nando_id	nando_uid	nando_label_ja	nando_label_en	kegg_id	property	kegg_label_ja	kegg_label_en	kegg_url
NANDO:1200003	http://nanbyodata.jp/ontology/NANDO_1200003	脊髄性筋萎縮症	Spinal muscular atrophy	H00455	http://www.geneontology.org/formats/oboInOwl#hasDbXref	脊髄性筋萎縮症	Spinal muscular atrophy	https://identifiers.org/kegg.disease:H00455
NANDO:1200009	http://nanbyodata.jp/ontology/NANDO_1200009	進行性核上性麻痺	Progressive supranuclear palsy	H00077	http://www.geneontology.org/formats/oboInOwl#hasDbXref	進行性核上性麻痺	Progressive supranuclear palsy	https://identifiers.org/kegg.disease:H00077
NANDO:1200009	http://nanbyodata.jp/ontology/NANDO_1200009	進行性核上性麻痺	Progressive supranuclear palsy	H00077	http://www.geneontology.org/formats/oboInOwl#hasDbXref	進行性核上性麻痺	Steele-Richardson-Olszewski syndrome	https://identifiers.org/kegg.disease:H00077
NANDO:1200010	http://nanbyodata.jp/ontology/NANDO_1200010	パーキンソン病	Parkinson's disease	H00057	http://www.geneontology.org/formats/oboInOwl#hasDbXref	パーキンソン病	Parkinson disease	https://identifiers.org/kegg.disease:H00057
NANDO:1200012	http://nanbyodata.jp/ontology/NANDO_1200012	ハンチントン病	Huntington's disease	H00059	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ハンチントン病	Huntington disease	https://identifiers.org/kegg.disease:H00059
NANDO:1200014	http://nanbyodata.jp/ontology/NANDO_1200014	有棘赤血球舞踏病	Chorea-acanthocytosis	H01432	http://www.geneontology.org/formats/oboInOwl#hasDbXref	有棘赤血球を伴う舞踏病	Chorea-acanthocytosis	https://identifiers.org/kegg.disease:H01432
NANDO:1200014	http://nanbyodata.jp/ontology/NANDO_1200014	有棘赤血球舞踏病	Chorea-acanthocytosis	H01432	http://www.geneontology.org/formats/oboInOwl#hasDbXref	有棘赤血球を伴う舞踏病	Choreoacanthocytosis	https://identifiers.org/kegg.disease:H01432
NANDO:1200015	http://nanbyodata.jp/ontology/NANDO_1200015	Mcleod症候群	McLeod syndrome	H00655	http://www.geneontology.org/formats/oboInOwl#hasDbXref	McLeod 症候群	McLeod syndrome	https://identifiers.org/kegg.disease:H00655
NANDO:1200016	http://nanbyodata.jp/ontology/NANDO_1200016	シャルコー・マリー・トゥース病	Charcot-Marie-Tooth disease	H00264	http://www.geneontology.org/formats/oboInOwl#hasDbXref	シャルコー・マリー・トゥース病	Charcot-Marie-Tooth disease	https://identifiers.org/kegg.disease:H00264
NANDO:1200016	http://nanbyodata.jp/ontology/NANDO_1200016	シャルコー・マリー・トゥース病	Charcot-Marie-Tooth disease	H00264	http://www.geneontology.org/formats/oboInOwl#hasDbXref	遺伝性運動感覚ニューロパチー	Charcot-Marie-Tooth disease	https://identifiers.org/kegg.disease:H00264
NANDO:1200016	http://nanbyodata.jp/ontology/NANDO_1200016	シャルコー・マリー・トゥース病	Charcot-Marie-Tooth disease	H00264	http://www.geneontology.org/formats/oboInOwl#hasDbXref	シャルコー・マリー・トゥース病	Hereditary motor and sensory neuropathy	https://identifiers.org/kegg.disease:H00264
NANDO:1200016	http://nanbyodata.jp/ontology/NANDO_1200016	シャルコー・マリー・トゥース病	Charcot-Marie-Tooth disease	H00264	http://www.geneontology.org/formats/oboInOwl#hasDbXref	遺伝性運動感覚ニューロパチー	Hereditary motor and sensory neuropathy	https://identifiers.org/kegg.disease:H00264
NANDO:1200020	http://nanbyodata.jp/ontology/NANDO_1200020	重症筋無力症	Myasthenia gravis	H01594	http://www.geneontology.org/formats/oboInOwl#hasDbXref	重症筋無力症	Myasthenia gravis	https://identifiers.org/kegg.disease:H01594
NANDO:1200021	http://nanbyodata.jp/ontology/NANDO_1200021	先天性筋無力症候群	Congenital myasthenic syndrome	H00770	http://www.geneontology.org/formats/oboInOwl#hasDbXref	先天性筋無力症候群	Congenital myasthenic syndrome	https://identifiers.org/kegg.disease:H00770
NANDO:1200023	http://nanbyodata.jp/ontology/NANDO_1200023	多発性硬化症	Multiple sclerosis	H01490	http://www.geneontology.org/formats/oboInOwl#hasDbXref	多発性硬化症	Multiple sclerosis	https://identifiers.org/kegg.disease:H01490
NANDO:1200027	http://nanbyodata.jp/ontology/NANDO_1200027	視神経脊髄炎	Neuromyelitis optica spectrum disorders	H01491	http://www.geneontology.org/formats/oboInOwl#hasDbXref	視神経脊髄炎	Neuromyelitis optica	https://identifiers.org/kegg.disease:H01491
NANDO:1200027	http://nanbyodata.jp/ontology/NANDO_1200027	視神経脊髄炎	Neuromyelitis optica spectrum disorders	H01491	http://www.geneontology.org/formats/oboInOwl#hasDbXref	デビック病	Neuromyelitis optica	https://identifiers.org/kegg.disease:H01491
NANDO:1200027	http://nanbyodata.jp/ontology/NANDO_1200027	視神経脊髄炎	Neuromyelitis optica spectrum disorders	H01491	http://www.geneontology.org/formats/oboInOwl#hasDbXref	視神経脊髄炎	Devic disease	https://identifiers.org/kegg.disease:H01491
NANDO:1200027	http://nanbyodata.jp/ontology/NANDO_1200027	視神経脊髄炎	Neuromyelitis optica spectrum disorders	H01491	http://www.geneontology.org/formats/oboInOwl#hasDbXref	デビック病	Devic disease	https://identifiers.org/kegg.disease:H01491
NANDO:1200030	http://nanbyodata.jp/ontology/NANDO_1200030	慢性炎症性脱髄性多発神経炎	Chronic inflammatory demyelinating polyneuropathy	H01527	http://www.geneontology.org/formats/oboInOwl#hasDbXref	多巣性運動ニューロパチー	Chronic inflammatory demyelinating polyradiculoneuropathy	https://identifiers.org/kegg.disease:H01527
NANDO:1200030	http://nanbyodata.jp/ontology/NANDO_1200030	慢性炎症性脱髄性多発神経炎	Chronic inflammatory demyelinating polyneuropathy	H01527	http://www.geneontology.org/formats/oboInOwl#hasDbXref	慢性炎症性脱髄性多発神経炎	Chronic inflammatory demyelinating polyradiculoneuropathy	https://identifiers.org/kegg.disease:H01527
NANDO:1200031	http://nanbyodata.jp/ontology/NANDO_1200031	多巣性運動ニューロパチー	Multifocal motor neuropathy	H01527	http://www.geneontology.org/formats/oboInOwl#hasDbXref	多巣性運動ニューロパチー	Chronic inflammatory demyelinating polyradiculoneuropathy	https://identifiers.org/kegg.disease:H01527
NANDO:1200031	http://nanbyodata.jp/ontology/NANDO_1200031	多巣性運動ニューロパチー	Multifocal motor neuropathy	H01527	http://www.geneontology.org/formats/oboInOwl#hasDbXref	慢性炎症性脱髄性多発神経炎	Chronic inflammatory demyelinating polyradiculoneuropathy	https://identifiers.org/kegg.disease:H01527
NANDO:1200032	http://nanbyodata.jp/ontology/NANDO_1200032	封入体筋炎	Sporadic inclusion body myositis	H01505	http://www.geneontology.org/formats/oboInOwl#hasDbXref	封入体筋炎	Inclusion body myositis	https://identifiers.org/kegg.disease:H01505
NANDO:1200033	http://nanbyodata.jp/ontology/NANDO_1200033	クロウ・深瀬症候群	Crow-Fukase syndrome	H01461	http://www.geneontology.org/formats/oboInOwl#hasDbXref	クロウ・深瀬症候群	Crow-Fukase syndrome	https://identifiers.org/kegg.disease:H01461
NANDO:1200033	http://nanbyodata.jp/ontology/NANDO_1200033	クロウ・深瀬症候群	Crow-Fukase syndrome	H01461	http://www.geneontology.org/formats/oboInOwl#hasDbXref	POEMS 症候群	Crow-Fukase syndrome	https://identifiers.org/kegg.disease:H01461
NANDO:1200033	http://nanbyodata.jp/ontology/NANDO_1200033	クロウ・深瀬症候群	Crow-Fukase syndrome	H01461	http://www.geneontology.org/formats/oboInOwl#hasDbXref	クロウ・深瀬症候群	POEMS syndrome	https://identifiers.org/kegg.disease:H01461
NANDO:1200033	http://nanbyodata.jp/ontology/NANDO_1200033	クロウ・深瀬症候群	Crow-Fukase syndrome	H01461	http://www.geneontology.org/formats/oboInOwl#hasDbXref	POEMS 症候群	POEMS syndrome	https://identifiers.org/kegg.disease:H01461
NANDO:1200034	http://nanbyodata.jp/ontology/NANDO_1200034	多系統萎縮症	Multiple system atrophy	H01614	http://www.geneontology.org/formats/oboInOwl#hasDbXref	多系統萎縮症	Multiple system atrophy	https://identifiers.org/kegg.disease:H01614
NANDO:1200037	http://nanbyodata.jp/ontology/NANDO_1200037	脊髄小脳変性症	Spinocerebellar degeneration	H01616	http://www.geneontology.org/formats/oboInOwl#hasDbXref	脊髄小脳変性症	Spinocerebellar degeneration	https://identifiers.org/kegg.disease:H01616
NANDO:1200052	http://nanbyodata.jp/ontology/NANDO_1200052	痙性対麻痺	Hereditary spastic paraplegia	H00266	http://www.geneontology.org/formats/oboInOwl#hasDbXref	遺伝性痙性対麻痺	Hereditary spastic paraplegia	https://identifiers.org/kegg.disease:H00266
NANDO:1200055	http://nanbyodata.jp/ontology/NANDO_1200055	ライソゾーム病	Lysosomal storage disease	H01425	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ライソゾーム病 (リソソーム蓄積症)	Lysosomal storage disease	https://identifiers.org/kegg.disease:H01425
NANDO:1200056	http://nanbyodata.jp/ontology/NANDO_1200056	ゴーシェ病	Gaucher disease	H00126	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ゴーシェ病	Gaucher disease	https://identifiers.org/kegg.disease:H00126
NANDO:1200063	http://nanbyodata.jp/ontology/NANDO_1200063	ニーマン・ピック病C型	Niemann-Pick disease type C	H00136	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ニーマン・ピック病 C 型	Niemann-Pick disease type C	https://identifiers.org/kegg.disease:H00136
NANDO:1200066	http://nanbyodata.jp/ontology/NANDO_1200066	GM1ガングリオシドーシス	GM1 gangliosidosis	H00281	http://www.geneontology.org/formats/oboInOwl#hasDbXref	GM1 ガングリオシドーシス	GM1 gangliosidosis	https://identifiers.org/kegg.disease:H00281
NANDO:1200074	http://nanbyodata.jp/ontology/NANDO_1200074	クラッベ病	Krabbe disease	H00135	http://www.geneontology.org/formats/oboInOwl#hasDbXref	クラッベ病	Krabbe disease	https://identifiers.org/kegg.disease:H00135
NANDO:1200074	http://nanbyodata.jp/ontology/NANDO_1200074	クラッベ病	Krabbe disease	H00135	http://www.geneontology.org/formats/oboInOwl#hasDbXref	グロボイド細胞白質ジストロフィー	Krabbe disease	https://identifiers.org/kegg.disease:H00135
NANDO:1200074	http://nanbyodata.jp/ontology/NANDO_1200074	クラッベ病	Krabbe disease	H00135	http://www.geneontology.org/formats/oboInOwl#hasDbXref	クラッベ病	Globoid cell leukodystrophy	https://identifiers.org/kegg.disease:H00135
NANDO:1200074	http://nanbyodata.jp/ontology/NANDO_1200074	クラッベ病	Krabbe disease	H00135	http://www.geneontology.org/formats/oboInOwl#hasDbXref	グロボイド細胞白質ジストロフィー	Globoid cell leukodystrophy	https://identifiers.org/kegg.disease:H00135
NANDO:1200078	http://nanbyodata.jp/ontology/NANDO_1200078	異染性白質ジストロフィー	Metachromatic leukodystrophy	H00127	http://www.geneontology.org/formats/oboInOwl#hasDbXref	異染性白質ジストロフィー	Metachromatic leukodystrophy	https://identifiers.org/kegg.disease:H00127
NANDO:1200083	http://nanbyodata.jp/ontology/NANDO_1200083	マルチプルサルファターゼ欠損症	Multiple sulfatase deficiency	H00272	http://www.geneontology.org/formats/oboInOwl#hasDbXref	マルチプルスルファターゼ欠損症	Multiple sulfatase deficiency	https://identifiers.org/kegg.disease:H00272
NANDO:1200086	http://nanbyodata.jp/ontology/NANDO_1200086	ファーバー病	Farber disease	H00138	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ファーバー病	Farber disease	https://identifiers.org/kegg.disease:H00138
NANDO:1200086	http://nanbyodata.jp/ontology/NANDO_1200086	ファーバー病	Farber disease	H00138	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ファーバー脂肪性肉芽腫症	Farber disease	https://identifiers.org/kegg.disease:H00138
NANDO:1200086	http://nanbyodata.jp/ontology/NANDO_1200086	ファーバー病	Farber disease	H00138	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ファーバー病	Farber lipogranulomatosis	https://identifiers.org/kegg.disease:H00138
NANDO:1200086	http://nanbyodata.jp/ontology/NANDO_1200086	ファーバー病	Farber disease	H00138	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ファーバー脂肪性肉芽腫症	Farber lipogranulomatosis	https://identifiers.org/kegg.disease:H00138
NANDO:1200097	http://nanbyodata.jp/ontology/NANDO_1200097	Hunter症候群	Hunter syndrome	H00129	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ハンター症候群	Hunter syndrome	https://identifiers.org/kegg.disease:H00129
NANDO:1200097	http://nanbyodata.jp/ontology/NANDO_1200097	Hunter症候群	Hunter syndrome	H00129	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ムコ多糖症 II 型	Hunter syndrome	https://identifiers.org/kegg.disease:H00129
NANDO:1200097	http://nanbyodata.jp/ontology/NANDO_1200097	Hunter症候群	Hunter syndrome	H00129	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ハンター症候群	Mucopolysaccharidosis type II	https://identifiers.org/kegg.disease:H00129
NANDO:1200097	http://nanbyodata.jp/ontology/NANDO_1200097	Hunter症候群	Hunter syndrome	H00129	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ムコ多糖症 II 型	Mucopolysaccharidosis type II	https://identifiers.org/kegg.disease:H00129
NANDO:1200108	http://nanbyodata.jp/ontology/NANDO_1200108	マロトー・ラミー症候群	Maroteaux-Lamy syndrome	H00131	http://www.geneontology.org/formats/oboInOwl#hasDbXref	マロトー・ラミー症候群	Maroteaux-Lamy syndrome	https://identifiers.org/kegg.disease:H00131
NANDO:1200108	http://nanbyodata.jp/ontology/NANDO_1200108	マロトー・ラミー症候群	Maroteaux-Lamy syndrome	H00131	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ムコ多糖症 VI 型	Maroteaux-Lamy syndrome	https://identifiers.org/kegg.disease:H00131
NANDO:1200108	http://nanbyodata.jp/ontology/NANDO_1200108	マロトー・ラミー症候群	Maroteaux-Lamy syndrome	H00131	http://www.geneontology.org/formats/oboInOwl#hasDbXref	マロトー・ラミー症候群	Mucopolysaccharidosis type VI	https://identifiers.org/kegg.disease:H00131
NANDO:1200108	http://nanbyodata.jp/ontology/NANDO_1200108	マロトー・ラミー症候群	Maroteaux-Lamy syndrome	H00131	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ムコ多糖症 VI 型	Mucopolysaccharidosis type VI	https://identifiers.org/kegg.disease:H00131
NANDO:1200111	http://nanbyodata.jp/ontology/NANDO_1200111	Sly病	Sly syndrome	H00132	http://www.geneontology.org/formats/oboInOwl#hasDbXref	スライ症候群	Mucopolysaccharidosis type VII	https://identifiers.org/kegg.disease:H00132
NANDO:1200111	http://nanbyodata.jp/ontology/NANDO_1200111	Sly病	Sly syndrome	H00132	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ムコ多糖症 VII 型	Mucopolysaccharidosis type VII	https://identifiers.org/kegg.disease:H00132
NANDO:1200111	http://nanbyodata.jp/ontology/NANDO_1200111	Sly病	Sly syndrome	H00132	http://www.geneontology.org/formats/oboInOwl#hasDbXref	スライ症候群	Sly syndrome	https://identifiers.org/kegg.disease:H00132
NANDO:1200111	http://nanbyodata.jp/ontology/NANDO_1200111	Sly病	Sly syndrome	H00132	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ムコ多糖症 VII 型	Sly syndrome	https://identifiers.org/kegg.disease:H00132
NANDO:1200115	http://nanbyodata.jp/ontology/NANDO_1200115	ヒアルロニダーゼ欠損症	Hyaluronidase deficiency	H00133	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ヒアルロニダーゼ欠損症	Hyaluronidase deficiency	https://identifiers.org/kegg.disease:H00133
NANDO:1200115	http://nanbyodata.jp/ontology/NANDO_1200115	ヒアルロニダーゼ欠損症	Hyaluronidase deficiency	H00133	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ムコ多糖症 IX 型	Hyaluronidase deficiency	https://identifiers.org/kegg.disease:H00133
NANDO:1200115	http://nanbyodata.jp/ontology/NANDO_1200115	ヒアルロニダーゼ欠損症	Hyaluronidase deficiency	H00133	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ヒアルロニダーゼ欠損症	Mucopolysaccharidosis type IX	https://identifiers.org/kegg.disease:H00133
NANDO:1200115	http://nanbyodata.jp/ontology/NANDO_1200115	ヒアルロニダーゼ欠損症	Hyaluronidase deficiency	H00133	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ムコ多糖症 IX 型	Mucopolysaccharidosis type IX	https://identifiers.org/kegg.disease:H00133
NANDO:1200116	http://nanbyodata.jp/ontology/NANDO_1200116	シアリドーシス	Sialidosis	H00142	http://www.geneontology.org/formats/oboInOwl#hasDbXref	シアリドーシス	Sialidosis	https://identifiers.org/kegg.disease:H00142
NANDO:1200116	http://nanbyodata.jp/ontology/NANDO_1200116	シアリドーシス	Sialidosis	H00142	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ムコリピドーシス 1 型	Sialidosis	https://identifiers.org/kegg.disease:H00142
NANDO:1200116	http://nanbyodata.jp/ontology/NANDO_1200116	シアリドーシス	Sialidosis	H00142	http://www.geneontology.org/formats/oboInOwl#hasDbXref	シアリドーシス	Mucolipidosis I	https://identifiers.org/kegg.disease:H00142
NANDO:1200116	http://nanbyodata.jp/ontology/NANDO_1200116	シアリドーシス	Sialidosis	H00142	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ムコリピドーシス 1 型	Mucolipidosis I	https://identifiers.org/kegg.disease:H00142
NANDO:1200119	http://nanbyodata.jp/ontology/NANDO_1200119	ガラクトシアリドーシス	Galactosialidosis	H00276	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ガラクトシアリドーシス	Galactosialidosis	https://identifiers.org/kegg.disease:H00276
NANDO:1200119	http://nanbyodata.jp/ontology/NANDO_1200119	ガラクトシアリドーシス	Galactosialidosis	H00276	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ノイラミダーゼ欠損および β-ガラクトシダーゼ欠損症	Galactosialidosis	https://identifiers.org/kegg.disease:H00276
NANDO:1200119	http://nanbyodata.jp/ontology/NANDO_1200119	ガラクトシアリドーシス	Galactosialidosis	H00276	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ガラクトシアリドーシス	Neuraminidase deficiency with beta-galactosidase deficiency	https://identifiers.org/kegg.disease:H00276
NANDO:1200119	http://nanbyodata.jp/ontology/NANDO_1200119	ガラクトシアリドーシス	Galactosialidosis	H00276	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ノイラミダーゼ欠損および β-ガラクトシダーゼ欠損症	Neuraminidase deficiency with beta-galactosidase deficiency	https://identifiers.org/kegg.disease:H00276
NANDO:1200124	http://nanbyodata.jp/ontology/NANDO_1200124	ムコリピドーシスII型	Mucolipidosis II	H00143	http://www.geneontology.org/formats/oboInOwl#hasDbXref	I 細胞病	I-cell disease	https://identifiers.org/kegg.disease:H00143
NANDO:1200124	http://nanbyodata.jp/ontology/NANDO_1200124	ムコリピドーシスII型	Mucolipidosis II	H00143	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ムコリピドーシス II 型	I-cell disease	https://identifiers.org/kegg.disease:H00143
NANDO:1200124	http://nanbyodata.jp/ontology/NANDO_1200124	ムコリピドーシスII型	Mucolipidosis II	H00143	http://www.geneontology.org/formats/oboInOwl#hasDbXref	I 細胞病	Mucolipidosis II	https://identifiers.org/kegg.disease:H00143
NANDO:1200124	http://nanbyodata.jp/ontology/NANDO_1200124	ムコリピドーシスII型	Mucolipidosis II	H00143	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ムコリピドーシス II 型	Mucolipidosis II	https://identifiers.org/kegg.disease:H00143
NANDO:1200126	http://nanbyodata.jp/ontology/NANDO_1200126	α-マンノシドーシス	Alpha-mannosidosis	H00139	http://www.geneontology.org/formats/oboInOwl#hasDbXref	α-マンノシドーシス	alpha-Mannosidosis	https://identifiers.org/kegg.disease:H00139
NANDO:1200129	http://nanbyodata.jp/ontology/NANDO_1200129	β-マンノシドーシス	Beta-mannosidosis	H00140	http://www.geneontology.org/formats/oboInOwl#hasDbXref	β-マンノシドーシス	beta-Mannosidosis	https://identifiers.org/kegg.disease:H00140
NANDO:1200133	http://nanbyodata.jp/ontology/NANDO_1200133	アスパルチルグルコサミン尿症	Aspartylglucosaminuria	H00145	http://www.geneontology.org/formats/oboInOwl#hasDbXref	アスパルチルグルコサミン尿症	Aspartylglucosaminuria	https://identifiers.org/kegg.disease:H00145
NANDO:1200157	http://nanbyodata.jp/ontology/NANDO_1200157	ファブリー病	Fabry disease	H00125	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ファブリー病	Fabry disease	https://identifiers.org/kegg.disease:H00125
NANDO:1200157	http://nanbyodata.jp/ontology/NANDO_1200157	ファブリー病	Fabry disease	H00125	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ファブリー病	Anderson-Fabry disease	https://identifiers.org/kegg.disease:H00125
NANDO:1200161	http://nanbyodata.jp/ontology/NANDO_1200161	シスチン症	Cystinosis	H00275	http://www.geneontology.org/formats/oboInOwl#hasDbXref	シスチン症	Cystinosis	https://identifiers.org/kegg.disease:H00275
NANDO:1200165	http://nanbyodata.jp/ontology/NANDO_1200165	副腎白質ジストロフィー	Adrenoleukodystrophy	H00176	http://www.geneontology.org/formats/oboInOwl#hasDbXref	副腎白質ジストロフィー	Adrenoleukodystrophy	https://identifiers.org/kegg.disease:H00176
NANDO:1200173	http://nanbyodata.jp/ontology/NANDO_1200173	ミトコンドリア病	Mitochondrial diseases	H01427	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ミトコンドリア病	Mitochondrial disease	https://identifiers.org/kegg.disease:H01427
NANDO:1200176	http://nanbyodata.jp/ontology/NANDO_1200176	ミトコンドリア脳筋症・乳酸アシドーシス・脳卒中様発作症候群	Mitochondrial encephalomyopathy, lactic acidosis, and strokelike episodes syndrome	H01347	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ミトコンドリア脳筋症・乳酸アシドーシス・脳卒中様発作症候群	MELAS syndrome	https://identifiers.org/kegg.disease:H01347
NANDO:1200176	http://nanbyodata.jp/ontology/NANDO_1200176	ミトコンドリア脳筋症・乳酸アシドーシス・脳卒中様発作症候群	Mitochondrial encephalomyopathy, lactic acidosis, and strokelike episodes syndrome	H01347	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ミトコンドリア脳筋症・乳酸アシドーシス・脳卒中様発作症候群	Mitochondrial myopathy, Encephalopathy, Lactic Acidosis, Stroke-like episodes	https://identifiers.org/kegg.disease:H01347
NANDO:1200177	http://nanbyodata.jp/ontology/NANDO_1200177	赤色ぼろ線維・ミオクローヌスてんかん症候群	Myoclonus epilepsy associated with ragged-red fibers	H01356	http://www.geneontology.org/formats/oboInOwl#hasDbXref	赤色ぼろ線維・ミオクローヌスてんかん症候群	Fukuhara syndrome	https://identifiers.org/kegg.disease:H01356
NANDO:1200177	http://nanbyodata.jp/ontology/NANDO_1200177	赤色ぼろ線維・ミオクローヌスてんかん症候群	Myoclonus epilepsy associated with ragged-red fibers	H01356	http://www.geneontology.org/formats/oboInOwl#hasDbXref	MERRF 症候群	Fukuhara syndrome	https://identifiers.org/kegg.disease:H01356
NANDO:1200177	http://nanbyodata.jp/ontology/NANDO_1200177	赤色ぼろ線維・ミオクローヌスてんかん症候群	Myoclonus epilepsy associated with ragged-red fibers	H01356	http://www.geneontology.org/formats/oboInOwl#hasDbXref	福原病	Fukuhara syndrome	https://identifiers.org/kegg.disease:H01356
NANDO:1200177	http://nanbyodata.jp/ontology/NANDO_1200177	赤色ぼろ線維・ミオクローヌスてんかん症候群	Myoclonus epilepsy associated with ragged-red fibers	H01356	http://www.geneontology.org/formats/oboInOwl#hasDbXref	赤色ぼろ線維・ミオクローヌスてんかん症候群	MERRF syndrome	https://identifiers.org/kegg.disease:H01356
NANDO:1200177	http://nanbyodata.jp/ontology/NANDO_1200177	赤色ぼろ線維・ミオクローヌスてんかん症候群	Myoclonus epilepsy associated with ragged-red fibers	H01356	http://www.geneontology.org/formats/oboInOwl#hasDbXref	MERRF 症候群	MERRF syndrome	https://identifiers.org/kegg.disease:H01356
NANDO:1200177	http://nanbyodata.jp/ontology/NANDO_1200177	赤色ぼろ線維・ミオクローヌスてんかん症候群	Myoclonus epilepsy associated with ragged-red fibers	H01356	http://www.geneontology.org/formats/oboInOwl#hasDbXref	福原病	MERRF syndrome	https://identifiers.org/kegg.disease:H01356
NANDO:1200177	http://nanbyodata.jp/ontology/NANDO_1200177	赤色ぼろ線維・ミオクローヌスてんかん症候群	Myoclonus epilepsy associated with ragged-red fibers	H01356	http://www.geneontology.org/formats/oboInOwl#hasDbXref	赤色ぼろ線維・ミオクローヌスてんかん症候群	Myoclonic Epilepsy and Ragged-Red Fiber Disease	https://identifiers.org/kegg.disease:H01356
NANDO:1200177	http://nanbyodata.jp/ontology/NANDO_1200177	赤色ぼろ線維・ミオクローヌスてんかん症候群	Myoclonus epilepsy associated with ragged-red fibers	H01356	http://www.geneontology.org/formats/oboInOwl#hasDbXref	MERRF 症候群	Myoclonic Epilepsy and Ragged-Red Fiber Disease	https://identifiers.org/kegg.disease:H01356
NANDO:1200177	http://nanbyodata.jp/ontology/NANDO_1200177	赤色ぼろ線維・ミオクローヌスてんかん症候群	Myoclonus epilepsy associated with ragged-red fibers	H01356	http://www.geneontology.org/formats/oboInOwl#hasDbXref	福原病	Myoclonic Epilepsy and Ragged-Red Fiber Disease	https://identifiers.org/kegg.disease:H01356
NANDO:1200180	http://nanbyodata.jp/ontology/NANDO_1200180	複合体I欠損症	Mitochondrial complex I deficiency	H00473	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ミトコンドリア複合体 I 欠損症	Mitochondrial complex I deficiency	https://identifiers.org/kegg.disease:H00473
NANDO:1200183	http://nanbyodata.jp/ontology/NANDO_1200183	もやもや病	Moyamoya disease	H01396	http://www.geneontology.org/formats/oboInOwl#hasDbXref	もやもや病	Moyamoya disease	https://identifiers.org/kegg.disease:H01396
NANDO:1200186	http://nanbyodata.jp/ontology/NANDO_1200186	プリオン病	Prion disease	H00061	http://www.geneontology.org/formats/oboInOwl#hasDbXref	プリオン病	Prion disease	https://identifiers.org/kegg.disease:H00061
NANDO:1200186	http://nanbyodata.jp/ontology/NANDO_1200186	プリオン病	Prion disease	H00061	http://www.geneontology.org/formats/oboInOwl#hasDbXref	プリオン病	Creutzfeldt-Jacob disease (CJD)	https://identifiers.org/kegg.disease:H00061
NANDO:1200186	http://nanbyodata.jp/ontology/NANDO_1200186	プリオン病	Prion disease	H00061	http://www.geneontology.org/formats/oboInOwl#hasDbXref	プリオン病	Fatal familial insomnia (FFI)	https://identifiers.org/kegg.disease:H00061
NANDO:1200186	http://nanbyodata.jp/ontology/NANDO_1200186	プリオン病	Prion disease	H00061	http://www.geneontology.org/formats/oboInOwl#hasDbXref	プリオン病	Gerstmann-Straussler disease (GSD)	https://identifiers.org/kegg.disease:H00061
NANDO:1200186	http://nanbyodata.jp/ontology/NANDO_1200186	プリオン病	Prion disease	H00061	http://www.geneontology.org/formats/oboInOwl#hasDbXref	プリオン病	Gerstmann-Straussler-Scheinker disease (GSSD)	https://identifiers.org/kegg.disease:H00061
NANDO:1200195	http://nanbyodata.jp/ontology/NANDO_1200195	亜急性硬化性全脳炎	Subacute sclerosing panencephalitis	H01696	http://www.geneontology.org/formats/oboInOwl#hasDbXref	亜急性硬化性全脳炎	Subacute sclerosing panencephalitis	https://identifiers.org/kegg.disease:H01696
NANDO:1200205	http://nanbyodata.jp/ontology/NANDO_1200205	進行性多巣性白質脳症	Progressive multifocal leukoencephalopathy	H00370	http://www.geneontology.org/formats/oboInOwl#hasDbXref	進行性多巣性白質脳症	Progressive multifocal leukoencephalopathy	https://identifiers.org/kegg.disease:H00370
NANDO:1200208	http://nanbyodata.jp/ontology/NANDO_1200208	家族性特発性基底核石灰化症	Familial idiopathic basal ganglia calcification	H01574	http://www.geneontology.org/formats/oboInOwl#hasDbXref	家族性特発性基底核石灰化症	Familial idiopathic basal ganglia calcification	https://identifiers.org/kegg.disease:H01574
NANDO:1200208	http://nanbyodata.jp/ontology/NANDO_1200208	家族性特発性基底核石灰化症	Familial idiopathic basal ganglia calcification	H01574	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ファール病	Familial idiopathic basal ganglia calcification	https://identifiers.org/kegg.disease:H01574
NANDO:1200208	http://nanbyodata.jp/ontology/NANDO_1200208	家族性特発性基底核石灰化症	Familial idiopathic basal ganglia calcification	H01574	http://www.geneontology.org/formats/oboInOwl#hasDbXref	家族性特発性基底核石灰化症	Bilateral striopallidodentate calcinosis (BSPDC)	https://identifiers.org/kegg.disease:H01574
NANDO:1200208	http://nanbyodata.jp/ontology/NANDO_1200208	家族性特発性基底核石灰化症	Familial idiopathic basal ganglia calcification	H01574	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ファール病	Bilateral striopallidodentate calcinosis (BSPDC)	https://identifiers.org/kegg.disease:H01574
NANDO:1200208	http://nanbyodata.jp/ontology/NANDO_1200208	家族性特発性基底核石灰化症	Familial idiopathic basal ganglia calcification	H01574	http://www.geneontology.org/formats/oboInOwl#hasDbXref	家族性特発性基底核石灰化症	Fahr disease	https://identifiers.org/kegg.disease:H01574
NANDO:1200208	http://nanbyodata.jp/ontology/NANDO_1200208	家族性特発性基底核石灰化症	Familial idiopathic basal ganglia calcification	H01574	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ファール病	Fahr disease	https://identifiers.org/kegg.disease:H01574
NANDO:1200216	http://nanbyodata.jp/ontology/NANDO_1200216	遠位型ミオパチー	Distal myopathy	H00594	http://www.geneontology.org/formats/oboInOwl#hasDbXref	遠位型ミオパチー	Distal myopathy	https://identifiers.org/kegg.disease:H00594
NANDO:1200220	http://nanbyodata.jp/ontology/NANDO_1200220	ベスレムミオパチー	Bethlem Myopathy	H01340	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ベスレムミオパチー	Bethlem myopathy	https://identifiers.org/kegg.disease:H01340
NANDO:1200222	http://nanbyodata.jp/ontology/NANDO_1200222	ダノン病	Danon disease	H00150	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ダノン病	Danon disease	https://identifiers.org/kegg.disease:H00150
NANDO:1200222	http://nanbyodata.jp/ontology/NANDO_1200222	ダノン病	Danon disease	H00150	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ダノン病	X-linked vacuolar cardiomyopathy and myopathy	https://identifiers.org/kegg.disease:H00150
NANDO:1200226	http://nanbyodata.jp/ontology/NANDO_1200226	神経線維腫症I型	Neurofibromatosis type 1	H01437	http://www.geneontology.org/formats/oboInOwl#hasDbXref	レックリングハウゼン病	Neurofibromatosis type 1	https://identifiers.org/kegg.disease:H01437
NANDO:1200226	http://nanbyodata.jp/ontology/NANDO_1200226	神経線維腫症I型	Neurofibromatosis type 1	H01437	http://www.geneontology.org/formats/oboInOwl#hasDbXref	神経線維腫症 I 型	Neurofibromatosis type 1	https://identifiers.org/kegg.disease:H01437
NANDO:1200226	http://nanbyodata.jp/ontology/NANDO_1200226	神経線維腫症I型	Neurofibromatosis type 1	H01437	http://www.geneontology.org/formats/oboInOwl#hasDbXref	レックリングハウゼン病	Von Recklinghausen disease	https://identifiers.org/kegg.disease:H01437
NANDO:1200226	http://nanbyodata.jp/ontology/NANDO_1200226	神経線維腫症I型	Neurofibromatosis type 1	H01437	http://www.geneontology.org/formats/oboInOwl#hasDbXref	神経線維腫症 I 型	Von Recklinghausen disease	https://identifiers.org/kegg.disease:H01437
NANDO:1200227	http://nanbyodata.jp/ontology/NANDO_1200227	神経線維腫症II型	Neurofibromatosis type 2	H01438	http://www.geneontology.org/formats/oboInOwl#hasDbXref	神経線維腫症 II 型	Neurofibromatosis type 2	https://identifiers.org/kegg.disease:H01438
NANDO:1200228	http://nanbyodata.jp/ontology/NANDO_1200228	天疱瘡	Pemphigus	H01648	http://www.geneontology.org/formats/oboInOwl#hasDbXref	天疱瘡	Pemphigus	https://identifiers.org/kegg.disease:H01648
NANDO:1200235	http://nanbyodata.jp/ontology/NANDO_1200235	単純型表皮水疱症	Epidermolysis bullosa simplex	H00584	http://www.geneontology.org/formats/oboInOwl#hasDbXref	単純型表皮水疱症	Epidermolysis bullosa simplex	https://identifiers.org/kegg.disease:H00584
NANDO:1200236	http://nanbyodata.jp/ontology/NANDO_1200236	接合部型表皮水疱症	Junctional epidermolysis bullosa	H00586	http://www.geneontology.org/formats/oboInOwl#hasDbXref	接合部型表皮水疱症	Epidermolysis bullosa, junctional	https://identifiers.org/kegg.disease:H00586
NANDO:1200239	http://nanbyodata.jp/ontology/NANDO_1200239	キンドラー症候群	Kindler syndrome	H00588	http://www.geneontology.org/formats/oboInOwl#hasDbXref	キンドラー症候群	Kindler syndrome	https://identifiers.org/kegg.disease:H00588
NANDO:1200240	http://nanbyodata.jp/ontology/NANDO_1200240	膿疱性乾癬（汎発型）	Pustular psoriasis	H01663	http://www.geneontology.org/formats/oboInOwl#hasDbXref	膿疱性乾癬	Pustular psoriasis	https://identifiers.org/kegg.disease:H01663
NANDO:1200245	http://nanbyodata.jp/ontology/NANDO_1200245	スティーヴンス・ジョンソン症候群	Stevens-Johnson syndrome	H01694	http://www.geneontology.org/formats/oboInOwl#hasDbXref	中毒性表皮壊死症	Stevens-Johnson syndrome	https://identifiers.org/kegg.disease:H01694
NANDO:1200245	http://nanbyodata.jp/ontology/NANDO_1200245	スティーヴンス・ジョンソン症候群	Stevens-Johnson syndrome	H01694	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ライエル症候群	Stevens-Johnson syndrome	https://identifiers.org/kegg.disease:H01694
NANDO:1200245	http://nanbyodata.jp/ontology/NANDO_1200245	スティーヴンス・ジョンソン症候群	Stevens-Johnson syndrome	H01694	http://www.geneontology.org/formats/oboInOwl#hasDbXref	スティーブンス・ジョンソン症候群	Stevens-Johnson syndrome	https://identifiers.org/kegg.disease:H01694
NANDO:1200245	http://nanbyodata.jp/ontology/NANDO_1200245	スティーヴンス・ジョンソン症候群	Stevens-Johnson syndrome	H01694	http://www.geneontology.org/formats/oboInOwl#hasDbXref	重症多形滲出性紅斑	Stevens-Johnson syndrome	https://identifiers.org/kegg.disease:H01694
NANDO:1200245	http://nanbyodata.jp/ontology/NANDO_1200245	スティーヴンス・ジョンソン症候群	Stevens-Johnson syndrome	H01694	http://www.geneontology.org/formats/oboInOwl#hasDbXref	中毒性表皮壊死症	Toxic epidermal necrolysis	https://identifiers.org/kegg.disease:H01694
NANDO:1200245	http://nanbyodata.jp/ontology/NANDO_1200245	スティーヴンス・ジョンソン症候群	Stevens-Johnson syndrome	H01694	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ライエル症候群	Toxic epidermal necrolysis	https://identifiers.org/kegg.disease:H01694
NANDO:1200245	http://nanbyodata.jp/ontology/NANDO_1200245	スティーヴンス・ジョンソン症候群	Stevens-Johnson syndrome	H01694	http://www.geneontology.org/formats/oboInOwl#hasDbXref	スティーブンス・ジョンソン症候群	Toxic epidermal necrolysis	https://identifiers.org/kegg.disease:H01694
NANDO:1200245	http://nanbyodata.jp/ontology/NANDO_1200245	スティーヴンス・ジョンソン症候群	Stevens-Johnson syndrome	H01694	http://www.geneontology.org/formats/oboInOwl#hasDbXref	重症多形滲出性紅斑	Toxic epidermal necrolysis	https://identifiers.org/kegg.disease:H01694
NANDO:1200245	http://nanbyodata.jp/ontology/NANDO_1200245	スティーヴンス・ジョンソン症候群	Stevens-Johnson syndrome	H01694	http://www.geneontology.org/formats/oboInOwl#hasDbXref	中毒性表皮壊死症	Lyell syndrome	https://identifiers.org/kegg.disease:H01694
NANDO:1200245	http://nanbyodata.jp/ontology/NANDO_1200245	スティーヴンス・ジョンソン症候群	Stevens-Johnson syndrome	H01694	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ライエル症候群	Lyell syndrome	https://identifiers.org/kegg.disease:H01694
NANDO:1200245	http://nanbyodata.jp/ontology/NANDO_1200245	スティーヴンス・ジョンソン症候群	Stevens-Johnson syndrome	H01694	http://www.geneontology.org/formats/oboInOwl#hasDbXref	スティーブンス・ジョンソン症候群	Lyell syndrome	https://identifiers.org/kegg.disease:H01694
NANDO:1200245	http://nanbyodata.jp/ontology/NANDO_1200245	スティーヴンス・ジョンソン症候群	Stevens-Johnson syndrome	H01694	http://www.geneontology.org/formats/oboInOwl#hasDbXref	重症多形滲出性紅斑	Lyell syndrome	https://identifiers.org/kegg.disease:H01694
NANDO:1200246	http://nanbyodata.jp/ontology/NANDO_1200246	中毒性表皮壊死症	Toxic epidermal necrolysis	H01694	http://www.geneontology.org/formats/oboInOwl#hasDbXref	中毒性表皮壊死症	Stevens-Johnson syndrome	https://identifiers.org/kegg.disease:H01694
NANDO:1200246	http://nanbyodata.jp/ontology/NANDO_1200246	中毒性表皮壊死症	Toxic epidermal necrolysis	H01694	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ライエル症候群	Stevens-Johnson syndrome	https://identifiers.org/kegg.disease:H01694
NANDO:1200246	http://nanbyodata.jp/ontology/NANDO_1200246	中毒性表皮壊死症	Toxic epidermal necrolysis	H01694	http://www.geneontology.org/formats/oboInOwl#hasDbXref	スティーブンス・ジョンソン症候群	Stevens-Johnson syndrome	https://identifiers.org/kegg.disease:H01694
NANDO:1200246	http://nanbyodata.jp/ontology/NANDO_1200246	中毒性表皮壊死症	Toxic epidermal necrolysis	H01694	http://www.geneontology.org/formats/oboInOwl#hasDbXref	重症多形滲出性紅斑	Stevens-Johnson syndrome	https://identifiers.org/kegg.disease:H01694
NANDO:1200246	http://nanbyodata.jp/ontology/NANDO_1200246	中毒性表皮壊死症	Toxic epidermal necrolysis	H01694	http://www.geneontology.org/formats/oboInOwl#hasDbXref	中毒性表皮壊死症	Toxic epidermal necrolysis	https://identifiers.org/kegg.disease:H01694
NANDO:1200246	http://nanbyodata.jp/ontology/NANDO_1200246	中毒性表皮壊死症	Toxic epidermal necrolysis	H01694	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ライエル症候群	Toxic epidermal necrolysis	https://identifiers.org/kegg.disease:H01694
NANDO:1200246	http://nanbyodata.jp/ontology/NANDO_1200246	中毒性表皮壊死症	Toxic epidermal necrolysis	H01694	http://www.geneontology.org/formats/oboInOwl#hasDbXref	スティーブンス・ジョンソン症候群	Toxic epidermal necrolysis	https://identifiers.org/kegg.disease:H01694
NANDO:1200246	http://nanbyodata.jp/ontology/NANDO_1200246	中毒性表皮壊死症	Toxic epidermal necrolysis	H01694	http://www.geneontology.org/formats/oboInOwl#hasDbXref	重症多形滲出性紅斑	Toxic epidermal necrolysis	https://identifiers.org/kegg.disease:H01694
NANDO:1200246	http://nanbyodata.jp/ontology/NANDO_1200246	中毒性表皮壊死症	Toxic epidermal necrolysis	H01694	http://www.geneontology.org/formats/oboInOwl#hasDbXref	中毒性表皮壊死症	Lyell syndrome	https://identifiers.org/kegg.disease:H01694
NANDO:1200246	http://nanbyodata.jp/ontology/NANDO_1200246	中毒性表皮壊死症	Toxic epidermal necrolysis	H01694	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ライエル症候群	Lyell syndrome	https://identifiers.org/kegg.disease:H01694
NANDO:1200246	http://nanbyodata.jp/ontology/NANDO_1200246	中毒性表皮壊死症	Toxic epidermal necrolysis	H01694	http://www.geneontology.org/formats/oboInOwl#hasDbXref	スティーブンス・ジョンソン症候群	Lyell syndrome	https://identifiers.org/kegg.disease:H01694
NANDO:1200246	http://nanbyodata.jp/ontology/NANDO_1200246	中毒性表皮壊死症	Toxic epidermal necrolysis	H01694	http://www.geneontology.org/formats/oboInOwl#hasDbXref	重症多形滲出性紅斑	Lyell syndrome	https://identifiers.org/kegg.disease:H01694
NANDO:1200258	http://nanbyodata.jp/ontology/NANDO_1200258	巨細胞性動脈炎	Giant cell arteritis	H01698	http://www.geneontology.org/formats/oboInOwl#hasDbXref	側頭動脈炎	Giant cell arteritis	https://identifiers.org/kegg.disease:H01698
NANDO:1200258	http://nanbyodata.jp/ontology/NANDO_1200258	巨細胞性動脈炎	Giant cell arteritis	H01698	http://www.geneontology.org/formats/oboInOwl#hasDbXref	巨細胞性動脈炎	Giant cell arteritis	https://identifiers.org/kegg.disease:H01698
NANDO:1200258	http://nanbyodata.jp/ontology/NANDO_1200258	巨細胞性動脈炎	Giant cell arteritis	H01698	http://www.geneontology.org/formats/oboInOwl#hasDbXref	側頭動脈炎	Temporal arteritis	https://identifiers.org/kegg.disease:H01698
NANDO:1200258	http://nanbyodata.jp/ontology/NANDO_1200258	巨細胞性動脈炎	Giant cell arteritis	H01698	http://www.geneontology.org/formats/oboInOwl#hasDbXref	巨細胞性動脈炎	Temporal arteritis	https://identifiers.org/kegg.disease:H01698
NANDO:1200261	http://nanbyodata.jp/ontology/NANDO_1200261	結節性多発動脈炎	Polyarteritis nodosa	H01382	http://www.geneontology.org/formats/oboInOwl#hasDbXref	結節性多発動脈炎	ADA2 deficiency	https://identifiers.org/kegg.disease:H01382
NANDO:1200261	http://nanbyodata.jp/ontology/NANDO_1200261	結節性多発動脈炎	Polyarteritis nodosa	H01382	http://www.geneontology.org/formats/oboInOwl#hasDbXref	血管炎・自己炎症・免疫不全・血液学的異常症候群	ADA2 deficiency	https://identifiers.org/kegg.disease:H01382
NANDO:1200261	http://nanbyodata.jp/ontology/NANDO_1200261	結節性多発動脈炎	Polyarteritis nodosa	H01382	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ADA2 欠損症	ADA2 deficiency	https://identifiers.org/kegg.disease:H01382
NANDO:1200261	http://nanbyodata.jp/ontology/NANDO_1200261	結節性多発動脈炎	Polyarteritis nodosa	H01382	http://www.geneontology.org/formats/oboInOwl#hasDbXref	結節性多発動脈炎	Polyarteritis nodosa	https://identifiers.org/kegg.disease:H01382
NANDO:1200261	http://nanbyodata.jp/ontology/NANDO_1200261	結節性多発動脈炎	Polyarteritis nodosa	H01382	http://www.geneontology.org/formats/oboInOwl#hasDbXref	血管炎・自己炎症・免疫不全・血液学的異常症候群	Polyarteritis nodosa	https://identifiers.org/kegg.disease:H01382
NANDO:1200261	http://nanbyodata.jp/ontology/NANDO_1200261	結節性多発動脈炎	Polyarteritis nodosa	H01382	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ADA2 欠損症	Polyarteritis nodosa	https://identifiers.org/kegg.disease:H01382
NANDO:1200261	http://nanbyodata.jp/ontology/NANDO_1200261	結節性多発動脈炎	Polyarteritis nodosa	H01382	http://www.geneontology.org/formats/oboInOwl#hasDbXref	結節性多発動脈炎	Vasculitis, autoinflammation, immunodeficiency, and hematologic defects syndrome	https://identifiers.org/kegg.disease:H01382
NANDO:1200261	http://nanbyodata.jp/ontology/NANDO_1200261	結節性多発動脈炎	Polyarteritis nodosa	H01382	http://www.geneontology.org/formats/oboInOwl#hasDbXref	血管炎・自己炎症・免疫不全・血液学的異常症候群	Vasculitis, autoinflammation, immunodeficiency, and hematologic defects syndrome	https://identifiers.org/kegg.disease:H01382
NANDO:1200261	http://nanbyodata.jp/ontology/NANDO_1200261	結節性多発動脈炎	Polyarteritis nodosa	H01382	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ADA2 欠損症	Vasculitis, autoinflammation, immunodeficiency, and hematologic defects syndrome	https://identifiers.org/kegg.disease:H01382
NANDO:1200262	http://nanbyodata.jp/ontology/NANDO_1200262	顕微鏡的多発血管炎	Microscopic polyangiitis	H01658	http://www.geneontology.org/formats/oboInOwl#hasDbXref	顕微鏡的多発血管炎	Microscopic polyangiitis	https://identifiers.org/kegg.disease:H01658
NANDO:1200263	http://nanbyodata.jp/ontology/NANDO_1200263	多発血管炎性肉芽腫症	Granulomatosis with polyangiitis	H01655	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ウェゲナー肉芽腫症	Granulomatosis with polyangiitis	https://identifiers.org/kegg.disease:H01655
NANDO:1200263	http://nanbyodata.jp/ontology/NANDO_1200263	多発血管炎性肉芽腫症	Granulomatosis with polyangiitis	H01655	http://www.geneontology.org/formats/oboInOwl#hasDbXref	多発血管炎性肉芽腫症	Granulomatosis with polyangiitis	https://identifiers.org/kegg.disease:H01655
NANDO:1200263	http://nanbyodata.jp/ontology/NANDO_1200263	多発血管炎性肉芽腫症	Granulomatosis with polyangiitis	H01655	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ウェゲナー肉芽腫症	Wegener granulomatosis	https://identifiers.org/kegg.disease:H01655
NANDO:1200263	http://nanbyodata.jp/ontology/NANDO_1200263	多発血管炎性肉芽腫症	Granulomatosis with polyangiitis	H01655	http://www.geneontology.org/formats/oboInOwl#hasDbXref	多発血管炎性肉芽腫症	Wegener granulomatosis	https://identifiers.org/kegg.disease:H01655
NANDO:1200264	http://nanbyodata.jp/ontology/NANDO_1200264	好酸球性多発血管炎性肉芽腫症	Eosinophilic granulomatosis with polyangiitis	H01468	http://www.geneontology.org/formats/oboInOwl#hasDbXref	好酸球性多発血管炎性肉芽腫症	Eosinophilic granulomatosis with polyangiitis	https://identifiers.org/kegg.disease:H01468
NANDO:1200264	http://nanbyodata.jp/ontology/NANDO_1200264	好酸球性多発血管炎性肉芽腫症	Eosinophilic granulomatosis with polyangiitis	H01468	http://www.geneontology.org/formats/oboInOwl#hasDbXref	チャーグストラウス症候群	Eosinophilic granulomatosis with polyangiitis	https://identifiers.org/kegg.disease:H01468
NANDO:1200264	http://nanbyodata.jp/ontology/NANDO_1200264	好酸球性多発血管炎性肉芽腫症	Eosinophilic granulomatosis with polyangiitis	H01468	http://www.geneontology.org/formats/oboInOwl#hasDbXref	好酸球性多発血管炎性肉芽腫症	Churg-Strauss syndrome	https://identifiers.org/kegg.disease:H01468
NANDO:1200264	http://nanbyodata.jp/ontology/NANDO_1200264	好酸球性多発血管炎性肉芽腫症	Eosinophilic granulomatosis with polyangiitis	H01468	http://www.geneontology.org/formats/oboInOwl#hasDbXref	チャーグストラウス症候群	Churg-Strauss syndrome	https://identifiers.org/kegg.disease:H01468
NANDO:1200266	http://nanbyodata.jp/ontology/NANDO_1200266	バージャー病	Buerger's disease	H01625	http://www.geneontology.org/formats/oboInOwl#hasDbXref	バージャー病	Thromboangiitis obliterans	https://identifiers.org/kegg.disease:H01625
NANDO:1200266	http://nanbyodata.jp/ontology/NANDO_1200266	バージャー病	Buerger's disease	H01625	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ビュルガー病	Thromboangiitis obliterans	https://identifiers.org/kegg.disease:H01625
NANDO:1200266	http://nanbyodata.jp/ontology/NANDO_1200266	バージャー病	Buerger's disease	H01625	http://www.geneontology.org/formats/oboInOwl#hasDbXref	閉塞性血栓血管炎	Thromboangiitis obliterans	https://identifiers.org/kegg.disease:H01625
NANDO:1200266	http://nanbyodata.jp/ontology/NANDO_1200266	バージャー病	Buerger's disease	H01625	http://www.geneontology.org/formats/oboInOwl#hasDbXref	バージャー病	Buerger disease	https://identifiers.org/kegg.disease:H01625
NANDO:1200266	http://nanbyodata.jp/ontology/NANDO_1200266	バージャー病	Buerger's disease	H01625	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ビュルガー病	Buerger disease	https://identifiers.org/kegg.disease:H01625
NANDO:1200266	http://nanbyodata.jp/ontology/NANDO_1200266	バージャー病	Buerger's disease	H01625	http://www.geneontology.org/formats/oboInOwl#hasDbXref	閉塞性血栓血管炎	Buerger disease	https://identifiers.org/kegg.disease:H01625
NANDO:1200272	http://nanbyodata.jp/ontology/NANDO_1200272	全身性エリテマトーデス	Systemic lupus erythematosus	H00080	http://www.geneontology.org/formats/oboInOwl#hasDbXref	全身性エリテマトーデス	Systemic lupus erythematosus	https://identifiers.org/kegg.disease:H00080
NANDO:1200273	http://nanbyodata.jp/ontology/NANDO_1200273	皮膚筋炎／多発性筋炎	Dermatomyositis/Polymyositis	H01604	http://www.geneontology.org/formats/oboInOwl#hasDbXref	皮膚筋炎/多発性筋炎	Polymyositis and dermatomyositis	https://identifiers.org/kegg.disease:H01604
NANDO:1200277	http://nanbyodata.jp/ontology/NANDO_1200277	全身性強皮症	Systemic sclerosis	H01492	http://www.geneontology.org/formats/oboInOwl#hasDbXref	全身性強皮症	Systemic scleroderma	https://identifiers.org/kegg.disease:H01492
NANDO:1200277	http://nanbyodata.jp/ontology/NANDO_1200277	全身性強皮症	Systemic sclerosis	H01492	http://www.geneontology.org/formats/oboInOwl#hasDbXref	全身性強皮症	Systemic sclerosis	https://identifiers.org/kegg.disease:H01492
NANDO:1200279	http://nanbyodata.jp/ontology/NANDO_1200279	シェーグレン症候群	Sjogren's syndrome	H01502	http://www.geneontology.org/formats/oboInOwl#hasDbXref	シェーグレン症候群	Sjogren syndrome	https://identifiers.org/kegg.disease:H01502
NANDO:1200284	http://nanbyodata.jp/ontology/NANDO_1200284	ベーチェット病	Behcet's disease	H01476	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ベーチェット病	Behcet disease	https://identifiers.org/kegg.disease:H01476
NANDO:1200284	http://nanbyodata.jp/ontology/NANDO_1200284	ベーチェット病	Behcet's disease	H01476	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ベーチェット病	Behcet syndrome	https://identifiers.org/kegg.disease:H01476
NANDO:1200286	http://nanbyodata.jp/ontology/NANDO_1200286	肥大型心筋症	Hypertrophic cardiomyopathy	H00292	http://www.geneontology.org/formats/oboInOwl#hasDbXref	肥大型心筋症	Hypertrophic cardiomyopathy	https://identifiers.org/kegg.disease:H00292
NANDO:1200292	http://nanbyodata.jp/ontology/NANDO_1200292	拘束型心筋症	Restrictive cardiomyopathy	H01219	http://www.geneontology.org/formats/oboInOwl#hasDbXref	拘束性心筋症	Restrictive cardiomyopathy	https://identifiers.org/kegg.disease:H01219
NANDO:1200295	http://nanbyodata.jp/ontology/NANDO_1200295	再生不良性貧血	Aplastic anemia	H01132	http://www.geneontology.org/formats/oboInOwl#hasDbXref	再生不良性貧血	Aplastic anemia	https://identifiers.org/kegg.disease:H01132
NANDO:1200304	http://nanbyodata.jp/ontology/NANDO_1200304	先天性角化不全症	Dyskeratosis congenita	H00507	http://www.geneontology.org/formats/oboInOwl#hasDbXref	先天性角化異常症	Dyskeratosis congenita	https://identifiers.org/kegg.disease:H00507
NANDO:1200305	http://nanbyodata.jp/ontology/NANDO_1200305	自己免疫性溶血性貧血	Autoimmune hemolytic anemia	H01585	http://www.geneontology.org/formats/oboInOwl#hasDbXref	自己免疫性溶血性貧血	Autoimmune hemolytic anemia	https://identifiers.org/kegg.disease:H01585
NANDO:1200311	http://nanbyodata.jp/ontology/NANDO_1200311	発作性夜間ヘモグロビン尿症	Paroxysmal nocturnal hemoglobinuria	H01053	http://www.geneontology.org/formats/oboInOwl#hasDbXref	発作性夜間ヘモグロビン尿症	Paroxysmal nocturnal hemoglobinuria	https://identifiers.org/kegg.disease:H01053
NANDO:1200316	http://nanbyodata.jp/ontology/NANDO_1200316	血栓性血小板減少性紫斑病	Thrombotic thrombocytopenic purpura	H00225	http://www.geneontology.org/formats/oboInOwl#hasDbXref	血栓性血小板減少性紫斑病	Thrombotic thrombocytopenic purpura	https://identifiers.org/kegg.disease:H00225
NANDO:1200316	http://nanbyodata.jp/ontology/NANDO_1200316	血栓性血小板減少性紫斑病	Thrombotic thrombocytopenic purpura	H00225	http://www.geneontology.org/formats/oboInOwl#hasDbXref	血栓性血小板減少性紫斑病	Moschcowitz disease	https://identifiers.org/kegg.disease:H00225
NANDO:1200316	http://nanbyodata.jp/ontology/NANDO_1200316	血栓性血小板減少性紫斑病	Thrombotic thrombocytopenic purpura	H00225	http://www.geneontology.org/formats/oboInOwl#hasDbXref	血栓性血小板減少性紫斑病	Schulman-Upshaw syndrome	https://identifiers.org/kegg.disease:H00225
NANDO:1200322	http://nanbyodata.jp/ontology/NANDO_1200322	細網異形成症	Reticular dysgenesis	H01128	http://www.geneontology.org/formats/oboInOwl#hasDbXref	細網異形成症	Reticular dysgenesis	https://identifiers.org/kegg.disease:H01128
NANDO:1200330	http://nanbyodata.jp/ontology/NANDO_1200330	ウィスコット・オルドリッチ症候群	Wiskott-Aldrich syndrome	H01523	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ウィスコット・アルドリッチ症候群	Wiskott-Aldrich syndrome	https://identifiers.org/kegg.disease:H01523
NANDO:1200331	http://nanbyodata.jp/ontology/NANDO_1200331	毛細血管拡張性運動失調症	Ataxia telangiectasia	H00064	http://www.geneontology.org/formats/oboInOwl#hasDbXref	毛細血管拡張性運動失調症	Ataxia telangiectasia	https://identifiers.org/kegg.disease:H00064
NANDO:1200331	http://nanbyodata.jp/ontology/NANDO_1200331	毛細血管拡張性運動失調症	Ataxia telangiectasia	H00064	http://www.geneontology.org/formats/oboInOwl#hasDbXref	毛細血管拡張性運動失調症	Louis-Bar syndrome	https://identifiers.org/kegg.disease:H00064
NANDO:1200331	http://nanbyodata.jp/ontology/NANDO_1200331	毛細血管拡張性運動失調症	Ataxia telangiectasia	H00064	http://www.geneontology.org/formats/oboInOwl#hasDbXref	毛細血管拡張性運動失調症	Boder-Sedgwick syndrome	https://identifiers.org/kegg.disease:H00064
NANDO:1200332	http://nanbyodata.jp/ontology/NANDO_1200332	ナイミーヘン染色体不安定症候群	Nijmegen breakage syndrome	H01344	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ナイミーヘン染色体不安定症候群	Nijmegen breakage syndrome	https://identifiers.org/kegg.disease:H01344
NANDO:1200333	http://nanbyodata.jp/ontology/NANDO_1200333	ブルーム症候群	Bloom syndrome	H01346	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ブルーム症候群	Bloom syndrome	https://identifiers.org/kegg.disease:H01346
NANDO:1200333	http://nanbyodata.jp/ontology/NANDO_1200333	ブルーム症候群	Bloom syndrome	H01346	http://www.geneontology.org/formats/oboInOwl#hasDbXref	MGRISCE1	Bloom syndrome	https://identifiers.org/kegg.disease:H01346
NANDO:1200333	http://nanbyodata.jp/ontology/NANDO_1200333	ブルーム症候群	Bloom syndrome	H01346	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ブルーム症候群	MGRISCE1	https://identifiers.org/kegg.disease:H01346
NANDO:1200333	http://nanbyodata.jp/ontology/NANDO_1200333	ブルーム症候群	Bloom syndrome	H01346	http://www.geneontology.org/formats/oboInOwl#hasDbXref	MGRISCE1	MGRISCE1	https://identifiers.org/kegg.disease:H01346
NANDO:1200336	http://nanbyodata.jp/ontology/NANDO_1200336	RIDDLE症候群	RIDDLE syndrome	H00962	http://www.geneontology.org/formats/oboInOwl#hasDbXref	RIDDLE 症候群	RIDDLE syndrome	https://identifiers.org/kegg.disease:H00962
NANDO:1200338	http://nanbyodata.jp/ontology/NANDO_1200338	ネザートン症候群	Netherton syndrome	H00671	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ネザートン症候群	Netherton syndrome	https://identifiers.org/kegg.disease:H00671
NANDO:1200344	http://nanbyodata.jp/ontology/NANDO_1200344	分類不能型免疫不全症	Common variable immunodeficiency	H00088	http://www.geneontology.org/formats/oboInOwl#hasDbXref	分類不能型免疫不全症	Common variable immunodeficiency	https://identifiers.org/kegg.disease:H00088
NANDO:1200352	http://nanbyodata.jp/ontology/NANDO_1200352	自己免疫性リンパ増殖症候群	Autoimmune lymphoproliferative syndrome	H00108	http://www.geneontology.org/formats/oboInOwl#hasDbXref	自己免疫性リンパ増殖症候群	Autoimmune lymphoproliferative syndromes	https://identifiers.org/kegg.disease:H00108
NANDO:1200355	http://nanbyodata.jp/ontology/NANDO_1200355	白血球接着不全症	Leukocyte adhesion deficiency	H00099	http://www.geneontology.org/formats/oboInOwl#hasDbXref	白血球粘着不全症	Leukocyte adhesion deficiency	https://identifiers.org/kegg.disease:H00099
NANDO:1200356	http://nanbyodata.jp/ontology/NANDO_1200356	シュワッハマン・ダイアモンド症候群	Shwachman-Diamond syndrome	H00439	http://www.geneontology.org/formats/oboInOwl#hasDbXref	シュバッハマン・ダイアモンド症候群	Shwachman-Diamond syndrome	https://identifiers.org/kegg.disease:H00439
NANDO:1200357	http://nanbyodata.jp/ontology/NANDO_1200357	慢性肉芽腫症	Chronic granulomatous disease	H00098	http://www.geneontology.org/formats/oboInOwl#hasDbXref	慢性肉芽腫症	Chronic granulomatous disease	https://identifiers.org/kegg.disease:H00098
NANDO:1200363	http://nanbyodata.jp/ontology/NANDO_1200363	慢性皮膚粘膜カンジダ症	Chronic mucocutaneous candidiasis	H01109	http://www.geneontology.org/formats/oboInOwl#hasDbXref	慢性皮膚粘膜カンジダ症	Chronic mucocutaneous candidiasis	https://identifiers.org/kegg.disease:H01109
NANDO:1200363	http://nanbyodata.jp/ontology/NANDO_1200363	慢性皮膚粘膜カンジダ症	Chronic mucocutaneous candidiasis	H01109	http://www.geneontology.org/formats/oboInOwl#hasDbXref	慢性皮膚粘膜カンジダ症	Familial candidiasis (CANDF)	https://identifiers.org/kegg.disease:H01109
NANDO:1200365	http://nanbyodata.jp/ontology/NANDO_1200365	遺伝性血管性浮腫	Hereditary angioedema	H01006	http://www.geneontology.org/formats/oboInOwl#hasDbXref	遺伝性血管性浮腫	Hereditary angioedema	https://identifiers.org/kegg.disease:H01006
NANDO:1200366	http://nanbyodata.jp/ontology/NANDO_1200366	IgＡ腎症	IgA nephropathy	H01581	http://www.geneontology.org/formats/oboInOwl#hasDbXref	IgA 腎症	IgA nephropathy	https://identifiers.org/kegg.disease:H01581
NANDO:1200366	http://nanbyodata.jp/ontology/NANDO_1200366	IgＡ腎症	IgA nephropathy	H01581	http://www.geneontology.org/formats/oboInOwl#hasDbXref	IgA 腎症	Berger disease	https://identifiers.org/kegg.disease:H01581
NANDO:1200367	http://nanbyodata.jp/ontology/NANDO_1200367	多発性嚢胞腎	Polycystic kidney disease	H00542	http://www.geneontology.org/formats/oboInOwl#hasDbXref	多発性嚢胞腎	Polycystic kidney disease	https://identifiers.org/kegg.disease:H00542
NANDO:1200375	http://nanbyodata.jp/ontology/NANDO_1200375	中枢性尿崩症	Central diabetes insipidus	H00253	http://www.geneontology.org/formats/oboInOwl#hasDbXref	中枢性尿崩症	Central diabetes insipidus	https://identifiers.org/kegg.disease:H00253
NANDO:1200375	http://nanbyodata.jp/ontology/NANDO_1200375	中枢性尿崩症	Central diabetes insipidus	H00253	http://www.geneontology.org/formats/oboInOwl#hasDbXref	神経下垂体性尿崩症	Central diabetes insipidus	https://identifiers.org/kegg.disease:H00253
NANDO:1200375	http://nanbyodata.jp/ontology/NANDO_1200375	中枢性尿崩症	Central diabetes insipidus	H00253	http://www.geneontology.org/formats/oboInOwl#hasDbXref	中枢性尿崩症	Neurohypophyseal diabetes insipidus	https://identifiers.org/kegg.disease:H00253
NANDO:1200375	http://nanbyodata.jp/ontology/NANDO_1200375	中枢性尿崩症	Central diabetes insipidus	H00253	http://www.geneontology.org/formats/oboInOwl#hasDbXref	神経下垂体性尿崩症	Neurohypophyseal diabetes insipidus	https://identifiers.org/kegg.disease:H00253
NANDO:1200388	http://nanbyodata.jp/ontology/NANDO_1200388	ゴナドトロピン分泌低下症	Hypogonadotropic hypogonadism	H00255	http://www.geneontology.org/formats/oboInOwl#hasDbXref	低ゴナドトロピン性性腺機能低下症	Hypogonadotropic hypogonadism	https://identifiers.org/kegg.disease:H00255
NANDO:1200396	http://nanbyodata.jp/ontology/NANDO_1200396	先天性副腎皮質酵素欠損症	Congenital adrenal enzyme deficiency	H00258	http://www.geneontology.org/formats/oboInOwl#hasDbXref	アルドステロン合成酵素欠損症	Aldosterone synthase deficiency	https://identifiers.org/kegg.disease:H00258
NANDO:1200396	http://nanbyodata.jp/ontology/NANDO_1200396	先天性副腎皮質酵素欠損症	Congenital adrenal enzyme deficiency	H00258	http://www.geneontology.org/formats/oboInOwl#hasDbXref	先天性副腎皮質酵素欠損症	Aldosterone synthase deficiency	https://identifiers.org/kegg.disease:H00258
NANDO:1200396	http://nanbyodata.jp/ontology/NANDO_1200396	先天性副腎皮質酵素欠損症	Congenital adrenal enzyme deficiency	H00258	http://www.geneontology.org/formats/oboInOwl#hasDbXref	アルドステロン合成酵素欠損症	Corticosterone methyloxidase type I deficiency	https://identifiers.org/kegg.disease:H00258
NANDO:1200396	http://nanbyodata.jp/ontology/NANDO_1200396	先天性副腎皮質酵素欠損症	Congenital adrenal enzyme deficiency	H00258	http://www.geneontology.org/formats/oboInOwl#hasDbXref	先天性副腎皮質酵素欠損症	Corticosterone methyloxidase type I deficiency	https://identifiers.org/kegg.disease:H00258
NANDO:1200396	http://nanbyodata.jp/ontology/NANDO_1200396	先天性副腎皮質酵素欠損症	Congenital adrenal enzyme deficiency	H00258	http://www.geneontology.org/formats/oboInOwl#hasDbXref	アルドステロン合成酵素欠損症	Corticosterone methyloxidase type II deficiency	https://identifiers.org/kegg.disease:H00258
NANDO:1200396	http://nanbyodata.jp/ontology/NANDO_1200396	先天性副腎皮質酵素欠損症	Congenital adrenal enzyme deficiency	H00258	http://www.geneontology.org/formats/oboInOwl#hasDbXref	先天性副腎皮質酵素欠損症	Corticosterone methyloxidase type II deficiency	https://identifiers.org/kegg.disease:H00258
NANDO:1200411	http://nanbyodata.jp/ontology/NANDO_1200411	アジソン病	Addison's disease	H01598	http://www.geneontology.org/formats/oboInOwl#hasDbXref	アジソン病	Addison disease	https://identifiers.org/kegg.disease:H01598
NANDO:1200411	http://nanbyodata.jp/ontology/NANDO_1200411	アジソン病	Addison's disease	H01598	http://www.geneontology.org/formats/oboInOwl#hasDbXref	副腎機能低下症	Addison disease	https://identifiers.org/kegg.disease:H01598
NANDO:1200411	http://nanbyodata.jp/ontology/NANDO_1200411	アジソン病	Addison's disease	H01598	http://www.geneontology.org/formats/oboInOwl#hasDbXref	原発性副腎機能不全	Addison disease	https://identifiers.org/kegg.disease:H01598
NANDO:1200411	http://nanbyodata.jp/ontology/NANDO_1200411	アジソン病	Addison's disease	H01598	http://www.geneontology.org/formats/oboInOwl#hasDbXref	アジソン病	Hypoadrenocorticism	https://identifiers.org/kegg.disease:H01598
NANDO:1200411	http://nanbyodata.jp/ontology/NANDO_1200411	アジソン病	Addison's disease	H01598	http://www.geneontology.org/formats/oboInOwl#hasDbXref	副腎機能低下症	Hypoadrenocorticism	https://identifiers.org/kegg.disease:H01598
NANDO:1200411	http://nanbyodata.jp/ontology/NANDO_1200411	アジソン病	Addison's disease	H01598	http://www.geneontology.org/formats/oboInOwl#hasDbXref	原発性副腎機能不全	Hypoadrenocorticism	https://identifiers.org/kegg.disease:H01598
NANDO:1200411	http://nanbyodata.jp/ontology/NANDO_1200411	アジソン病	Addison's disease	H01598	http://www.geneontology.org/formats/oboInOwl#hasDbXref	アジソン病	Primary adrenal insufficiency	https://identifiers.org/kegg.disease:H01598
NANDO:1200411	http://nanbyodata.jp/ontology/NANDO_1200411	アジソン病	Addison's disease	H01598	http://www.geneontology.org/formats/oboInOwl#hasDbXref	副腎機能低下症	Primary adrenal insufficiency	https://identifiers.org/kegg.disease:H01598
NANDO:1200411	http://nanbyodata.jp/ontology/NANDO_1200411	アジソン病	Addison's disease	H01598	http://www.geneontology.org/formats/oboInOwl#hasDbXref	原発性副腎機能不全	Primary adrenal insufficiency	https://identifiers.org/kegg.disease:H01598
NANDO:1200417	http://nanbyodata.jp/ontology/NANDO_1200417	特発性肺線維症	Idiopathic pulmonary fibrosis	H01299	http://www.geneontology.org/formats/oboInOwl#hasDbXref	特発性肺線維症	Idiopathic pulmonary fibrosis	https://identifiers.org/kegg.disease:H01299
NANDO:1200425	http://nanbyodata.jp/ontology/NANDO_1200425	肺動脈性肺高血圧症	Pulmonary arterial hypertension	H01621	http://www.geneontology.org/formats/oboInOwl#hasDbXref	肺動脈性肺高血圧症	Pulmonary arterial hypertension	https://identifiers.org/kegg.disease:H01621
NANDO:1200429	http://nanbyodata.jp/ontology/NANDO_1200429	慢性血栓塞栓性肺高血圧症	Chronic thromboembolic pulmonary hypertension	H01622	http://www.geneontology.org/formats/oboInOwl#hasDbXref	慢性血栓塞栓性肺高血圧症	Chronic thromboembolic pulmonary hypertension	https://identifiers.org/kegg.disease:H01622
NANDO:1200430	http://nanbyodata.jp/ontology/NANDO_1200430	リンパ脈管筋腫症	Lymphangioleiomyomatosis	H00896	http://www.geneontology.org/formats/oboInOwl#hasDbXref	リンパ脈管筋腫症	Lymphangioleiomyomatosis	https://identifiers.org/kegg.disease:H00896
NANDO:1200431	http://nanbyodata.jp/ontology/NANDO_1200431	網膜色素変性症	Retinitis pigmentosa	H00527	http://www.geneontology.org/formats/oboInOwl#hasDbXref	網膜色素変性	Retinitis pigmentosa	https://identifiers.org/kegg.disease:H00527
NANDO:1200437	http://nanbyodata.jp/ontology/NANDO_1200437	バッド・キアリ症候群	Budd-Chiari syndrome	H01433	http://www.geneontology.org/formats/oboInOwl#hasDbXref	バット・キアリ症候群	Budd-Chiari syndrome	https://identifiers.org/kegg.disease:H01433
NANDO:1200438	http://nanbyodata.jp/ontology/NANDO_1200438	特発性門脈圧亢進症	Idiopathic portal hypertension	H01686	http://www.geneontology.org/formats/oboInOwl#hasDbXref	バンチ症候群	Banti syndrome	https://identifiers.org/kegg.disease:H01686
NANDO:1200438	http://nanbyodata.jp/ontology/NANDO_1200438	特発性門脈圧亢進症	Idiopathic portal hypertension	H01686	http://www.geneontology.org/formats/oboInOwl#hasDbXref	特発性門脈圧亢進症	Banti syndrome	https://identifiers.org/kegg.disease:H01686
NANDO:1200438	http://nanbyodata.jp/ontology/NANDO_1200438	特発性門脈圧亢進症	Idiopathic portal hypertension	H01686	http://www.geneontology.org/formats/oboInOwl#hasDbXref	非硬変症性門脈線維症	Banti syndrome	https://identifiers.org/kegg.disease:H01686
NANDO:1200438	http://nanbyodata.jp/ontology/NANDO_1200438	特発性門脈圧亢進症	Idiopathic portal hypertension	H01686	http://www.geneontology.org/formats/oboInOwl#hasDbXref	バンチ症候群	Idiopathic portal hypertension	https://identifiers.org/kegg.disease:H01686
NANDO:1200438	http://nanbyodata.jp/ontology/NANDO_1200438	特発性門脈圧亢進症	Idiopathic portal hypertension	H01686	http://www.geneontology.org/formats/oboInOwl#hasDbXref	特発性門脈圧亢進症	Idiopathic portal hypertension	https://identifiers.org/kegg.disease:H01686
NANDO:1200438	http://nanbyodata.jp/ontology/NANDO_1200438	特発性門脈圧亢進症	Idiopathic portal hypertension	H01686	http://www.geneontology.org/formats/oboInOwl#hasDbXref	非硬変症性門脈線維症	Idiopathic portal hypertension	https://identifiers.org/kegg.disease:H01686
NANDO:1200438	http://nanbyodata.jp/ontology/NANDO_1200438	特発性門脈圧亢進症	Idiopathic portal hypertension	H01686	http://www.geneontology.org/formats/oboInOwl#hasDbXref	バンチ症候群	Non-cirrhotic portal fibrosis	https://identifiers.org/kegg.disease:H01686
NANDO:1200438	http://nanbyodata.jp/ontology/NANDO_1200438	特発性門脈圧亢進症	Idiopathic portal hypertension	H01686	http://www.geneontology.org/formats/oboInOwl#hasDbXref	特発性門脈圧亢進症	Non-cirrhotic portal fibrosis	https://identifiers.org/kegg.disease:H01686
NANDO:1200438	http://nanbyodata.jp/ontology/NANDO_1200438	特発性門脈圧亢進症	Idiopathic portal hypertension	H01686	http://www.geneontology.org/formats/oboInOwl#hasDbXref	非硬変症性門脈線維症	Non-cirrhotic portal fibrosis	https://identifiers.org/kegg.disease:H01686
NANDO:1200439	http://nanbyodata.jp/ontology/NANDO_1200439	原発性胆汁性胆管炎	Primary biliary cholangitis	H01467	http://www.geneontology.org/formats/oboInOwl#hasDbXref	原発性胆汁性胆管炎	Primary biliary cholangitis	https://identifiers.org/kegg.disease:H01467
NANDO:1200439	http://nanbyodata.jp/ontology/NANDO_1200439	原発性胆汁性胆管炎	Primary biliary cholangitis	H01467	http://www.geneontology.org/formats/oboInOwl#hasDbXref	原発性胆汁性肝硬変	Primary biliary cholangitis	https://identifiers.org/kegg.disease:H01467
NANDO:1200439	http://nanbyodata.jp/ontology/NANDO_1200439	原発性胆汁性胆管炎	Primary biliary cholangitis	H01467	http://www.geneontology.org/formats/oboInOwl#hasDbXref	原発性胆汁性胆管炎	Primary biliary cirrhosis	https://identifiers.org/kegg.disease:H01467
NANDO:1200439	http://nanbyodata.jp/ontology/NANDO_1200439	原発性胆汁性胆管炎	Primary biliary cholangitis	H01467	http://www.geneontology.org/formats/oboInOwl#hasDbXref	原発性胆汁性肝硬変	Primary biliary cirrhosis	https://identifiers.org/kegg.disease:H01467
NANDO:1200440	http://nanbyodata.jp/ontology/NANDO_1200440	原発性硬化性胆管炎	Primary sclerosing cholangitis	H01684	http://www.geneontology.org/formats/oboInOwl#hasDbXref	原発性硬化性胆管炎	Primary sclerosing cholangitis	https://identifiers.org/kegg.disease:H01684
NANDO:1200441	http://nanbyodata.jp/ontology/NANDO_1200441	自己免疫性肝炎	Autoimmune hepatitis	H01685	http://www.geneontology.org/formats/oboInOwl#hasDbXref	自己免疫性肝炎	Autoimmune hepatitis	https://identifiers.org/kegg.disease:H01685
NANDO:1200444	http://nanbyodata.jp/ontology/NANDO_1200444	クローン病	Crohn's disease	H00286	http://www.geneontology.org/formats/oboInOwl#hasDbXref	クローン病	Crohn disease	https://identifiers.org/kegg.disease:H00286
NANDO:1200449	http://nanbyodata.jp/ontology/NANDO_1200449	潰瘍性大腸炎	Ulcerative colitis	H01466	http://www.geneontology.org/formats/oboInOwl#hasDbXref	潰瘍性大腸炎	Ulcerative colitis	https://identifiers.org/kegg.disease:H01466
NANDO:1200456	http://nanbyodata.jp/ontology/NANDO_1200456	好酸球性食道炎	Eosinophilic esophagitis	H01361	http://www.geneontology.org/formats/oboInOwl#hasDbXref	好酸球性食道炎	Eosinophilic esophagitis	https://identifiers.org/kegg.disease:H01361
NANDO:1200458	http://nanbyodata.jp/ontology/NANDO_1200458	慢性特発性偽性腸閉塞症	Chronic idiopathic intestinal pseudo-obstruction	H01276	http://www.geneontology.org/formats/oboInOwl#hasDbXref	慢性特発性偽性腸閉塞症	CIIP	https://identifiers.org/kegg.disease:H01276
NANDO:1200458	http://nanbyodata.jp/ontology/NANDO_1200458	慢性特発性偽性腸閉塞症	Chronic idiopathic intestinal pseudo-obstruction	H01276	http://www.geneontology.org/formats/oboInOwl#hasDbXref	慢性特発性偽性腸閉塞症	Chronic idiopathic intestinal pseudo-obstruction	https://identifiers.org/kegg.disease:H01276
NANDO:1200461	http://nanbyodata.jp/ontology/NANDO_1200461	ルビンシュタイン・テイビ症候群	Rubinstein-Taybi syndrome	H00504	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ルビンシュタイン・テイビ症候群	Rubinstein-Taybi syndrome	https://identifiers.org/kegg.disease:H00504
NANDO:1200464	http://nanbyodata.jp/ontology/NANDO_1200464	チャージ症候群	CHARGE syndrome	H00556	http://www.geneontology.org/formats/oboInOwl#hasDbXref	チャージ症候群	CHARGE syndrome	https://identifiers.org/kegg.disease:H00556
NANDO:1200465	http://nanbyodata.jp/ontology/NANDO_1200465	クリオピリン関連周期熱症候群	Cryopyrin-associated periodic syndrome	H00282	http://www.geneontology.org/formats/oboInOwl#hasDbXref	クリオピリン関連周期熱症候群	Cryopyrin associated periodic syndrome	https://identifiers.org/kegg.disease:H00282
NANDO:1200469	http://nanbyodata.jp/ontology/NANDO_1200469	若年性特発性関節炎	Juvenile idiopathic arthritis	H01672	http://www.geneontology.org/formats/oboInOwl#hasDbXref	若年性特発性関節炎	Juvenile idiopathic arthritis	https://identifiers.org/kegg.disease:H01672
NANDO:1200472	http://nanbyodata.jp/ontology/NANDO_1200472	TNF受容体関連周期性症候群	TNF receptor-associated periodic fever syndrome	H00912	http://www.geneontology.org/formats/oboInOwl#hasDbXref	TNF受容体関連周期性症候群	Familial periodic fever	https://identifiers.org/kegg.disease:H00912
NANDO:1200472	http://nanbyodata.jp/ontology/NANDO_1200472	TNF受容体関連周期性症候群	TNF receptor-associated periodic fever syndrome	H00912	http://www.geneontology.org/formats/oboInOwl#hasDbXref	TNF受容体関連周期性症候群	Tumor necrosis factor receptor-associated periodic syndrome	https://identifiers.org/kegg.disease:H00912
NANDO:1200473	http://nanbyodata.jp/ontology/NANDO_1200473	非典型溶血性尿毒症症候群	Atypical hemolytic uremic syndrome	H01434	http://www.geneontology.org/formats/oboInOwl#hasDbXref	非典型溶血性尿毒症症候群	Atypical hemolytic uremic syndrome	https://identifiers.org/kegg.disease:H01434
NANDO:1200476	http://nanbyodata.jp/ontology/NANDO_1200476	ブラウ症候群	Blau syndrome	H00285	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ブラウ症候群	Blau syndrome	https://identifiers.org/kegg.disease:H00285
NANDO:1200478	http://nanbyodata.jp/ontology/NANDO_1200478	ネマリンミオパチー	Nemaline myopathy	H00698	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ネマリンミオパチー	Nemaline myopathy	https://identifiers.org/kegg.disease:H00698
NANDO:1200479	http://nanbyodata.jp/ontology/NANDO_1200479	セントラルコア病	Central core disease	H00699	http://www.geneontology.org/formats/oboInOwl#hasDbXref	セントラルコア病	Central core disease	https://identifiers.org/kegg.disease:H00699
NANDO:1200482	http://nanbyodata.jp/ontology/NANDO_1200482	中心核ミオパチー	Centronuclear myopathy	H00700	http://www.geneontology.org/formats/oboInOwl#hasDbXref	中心核ミオパチー	Centronuclear myopathy	https://identifiers.org/kegg.disease:H00700
NANDO:1200485	http://nanbyodata.jp/ontology/NANDO_1200485	マリネスコ・シェーグレン症候群	Marinesco-Sjogren syndrome	H01284	http://www.geneontology.org/formats/oboInOwl#hasDbXref	マリネスコ・シェーグレン症候群	Marinesco-Sjogren syndrome	https://identifiers.org/kegg.disease:H01284
NANDO:1200487	http://nanbyodata.jp/ontology/NANDO_1200487	ジストロフィン異常症	Dystrophinopathies	H00562	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ジストロフィン異常症	Dystrophinopathies	https://identifiers.org/kegg.disease:H00562
NANDO:1200490	http://nanbyodata.jp/ontology/NANDO_1200490	肢帯型筋ジストロフィー	Limb-girdle muscular dystrophy	H00593	http://www.geneontology.org/formats/oboInOwl#hasDbXref	肢帯型筋ジストロフィー	Limb-girdle muscular dystrophy	https://identifiers.org/kegg.disease:H00593
NANDO:1200491	http://nanbyodata.jp/ontology/NANDO_1200491	顔面肩甲上腕型筋ジストロフィー	Facioscapulohumeral muscular dystrophy	H00591	http://www.geneontology.org/formats/oboInOwl#hasDbXref	顔面肩甲上腕型筋ジストロフィー	Facioscapulohumeral muscular dystrophy	https://identifiers.org/kegg.disease:H00591
NANDO:1200492	http://nanbyodata.jp/ontology/NANDO_1200492	エメリー・ドレイフス型筋ジストロフィー	Emery-Dreifuss muscular dystrophy	H00563	http://www.geneontology.org/formats/oboInOwl#hasDbXref	エメリー・ドレフュス型筋ジストロフィー	Emery-Dreifuss muscular dystrophy	https://identifiers.org/kegg.disease:H00563
NANDO:1200497	http://nanbyodata.jp/ontology/NANDO_1200497	先天性ミオトニー	Myotonia congenita	H00705	http://www.geneontology.org/formats/oboInOwl#hasDbXref	先天性ミオトニー	Myotonia congenita	https://identifiers.org/kegg.disease:H00705
NANDO:1200500	http://nanbyodata.jp/ontology/NANDO_1200500	ナトリウムチャネルミオトニー	Sodium channel myotonia	H00744	http://www.geneontology.org/formats/oboInOwl#hasDbXref	カリウム惹起性ミオトニー	Sodium channel myotonia	https://identifiers.org/kegg.disease:H00744
NANDO:1200500	http://nanbyodata.jp/ontology/NANDO_1200500	ナトリウムチャネルミオトニー	Sodium channel myotonia	H00744	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ナトリウムチャネルミオトニー	Sodium channel myotonia	https://identifiers.org/kegg.disease:H00744
NANDO:1200500	http://nanbyodata.jp/ontology/NANDO_1200500	ナトリウムチャネルミオトニー	Sodium channel myotonia	H00744	http://www.geneontology.org/formats/oboInOwl#hasDbXref	カリウム惹起性ミオトニー	Potassium-aggravated myotonia	https://identifiers.org/kegg.disease:H00744
NANDO:1200500	http://nanbyodata.jp/ontology/NANDO_1200500	ナトリウムチャネルミオトニー	Sodium channel myotonia	H00744	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ナトリウムチャネルミオトニー	Potassium-aggravated myotonia	https://identifiers.org/kegg.disease:H00744
NANDO:1200501	http://nanbyodata.jp/ontology/NANDO_1200501	先天性パラミオトニー	Paramyotonia congenita	H00743	http://www.geneontology.org/formats/oboInOwl#hasDbXref	先天性パラミオトニー	Paramyotonia congenita	https://identifiers.org/kegg.disease:H00743
NANDO:1200502	http://nanbyodata.jp/ontology/NANDO_1200502	遺伝性周期性四肢麻痺	Hereditary periodic paralysis	H00215	http://www.geneontology.org/formats/oboInOwl#hasDbXref	遺伝性周期性四肢麻痺	Periodic paralysis	https://identifiers.org/kegg.disease:H00215
NANDO:1200506	http://nanbyodata.jp/ontology/NANDO_1200506	脊髄空洞症	Syringomyelia	H01675	http://www.geneontology.org/formats/oboInOwl#hasDbXref	脊髄空洞症	Syringomyelia	https://identifiers.org/kegg.disease:H01675
NANDO:1200511	http://nanbyodata.jp/ontology/NANDO_1200511	遺伝性ジストニア	Hereditary dystonia	H00831	http://www.geneontology.org/formats/oboInOwl#hasDbXref	遺伝性ジストニア	Primary dystonia	https://identifiers.org/kegg.disease:H00831
NANDO:1200525	http://nanbyodata.jp/ontology/NANDO_1200525	小児交互性片麻痺	Alternating hemiplegia of childhood	H00998	http://www.geneontology.org/formats/oboInOwl#hasDbXref	小児交互性片麻痺	Alternating hemiplegia of childhood	https://identifiers.org/kegg.disease:H00998
NANDO:1200542	http://nanbyodata.jp/ontology/NANDO_1200542	脳内鉄沈着神経変性症	Neurodegeneration with brain iron accumulation	H00833	http://www.geneontology.org/formats/oboInOwl#hasDbXref	脳の鉄沈着を伴う神経変性疾患	Neurodegeneration with brain iron accumulation	https://identifiers.org/kegg.disease:H00833
NANDO:1200548	http://nanbyodata.jp/ontology/NANDO_1200548	前頭側頭葉変性症	Frontotemporal lobar degeneration	H00078	http://www.geneontology.org/formats/oboInOwl#hasDbXref	前頭側頭葉変性症	Frontotemporal lobar degeneration	https://identifiers.org/kegg.disease:H00078
NANDO:1200554	http://nanbyodata.jp/ontology/NANDO_1200554	アレキサンダー病	Alexander disease	H00065	http://www.geneontology.org/formats/oboInOwl#hasDbXref	アレキサンダー病	Alexander disease	https://identifiers.org/kegg.disease:H00065
NANDO:1200575	http://nanbyodata.jp/ontology/NANDO_1200575	先天性大脳白質形成不全症	Congenital hypomyelinating leukodystrophy	H00679	http://www.geneontology.org/formats/oboInOwl#hasDbXref	先天性大脳白質形成不全症	Hypomyelinating leukodystrophy	https://identifiers.org/kegg.disease:H00679
NANDO:1200575	http://nanbyodata.jp/ontology/NANDO_1200575	先天性大脳白質形成不全症	Congenital hypomyelinating leukodystrophy	H00679	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ペリツェウス・メルツバッヘル病	Hypomyelinating leukodystrophy	https://identifiers.org/kegg.disease:H00679
NANDO:1200575	http://nanbyodata.jp/ontology/NANDO_1200575	先天性大脳白質形成不全症	Congenital hypomyelinating leukodystrophy	H00679	http://www.geneontology.org/formats/oboInOwl#hasDbXref	先天性大脳白質形成不全症	Pelizaeus-Merzbacher disease (PMD)	https://identifiers.org/kegg.disease:H00679
NANDO:1200575	http://nanbyodata.jp/ontology/NANDO_1200575	先天性大脳白質形成不全症	Congenital hypomyelinating leukodystrophy	H00679	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ペリツェウス・メルツバッヘル病	Pelizaeus-Merzbacher disease (PMD)	https://identifiers.org/kegg.disease:H00679
NANDO:1200580	http://nanbyodata.jp/ontology/NANDO_1200580	アラン・ハーンドン・タドリー症候群	Allan-Herndon-Dudley syndrome	H00650	http://www.geneontology.org/formats/oboInOwl#hasDbXref	Allan-Herndon-Dudley 症候群	Allan-Herndon-Dudley syndrome	https://identifiers.org/kegg.disease:H00650
NANDO:1200580	http://nanbyodata.jp/ontology/NANDO_1200580	アラン・ハーンドン・タドリー症候群	Allan-Herndon-Dudley syndrome	H00650	http://www.geneontology.org/formats/oboInOwl#hasDbXref	Allan-Herndon-Dudley 症候群	Monocarboxylate transporter 8 deficiency	https://identifiers.org/kegg.disease:H00650
NANDO:1200592	http://nanbyodata.jp/ontology/NANDO_1200592	ウエスト症候群	West syndrome	H01460	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ウエスト症候群	Infantile spasms	https://identifiers.org/kegg.disease:H01460
NANDO:1200592	http://nanbyodata.jp/ontology/NANDO_1200592	ウエスト症候群	West syndrome	H01460	http://www.geneontology.org/formats/oboInOwl#hasDbXref	点頭てんかん	Infantile spasms	https://identifiers.org/kegg.disease:H01460
NANDO:1200592	http://nanbyodata.jp/ontology/NANDO_1200592	ウエスト症候群	West syndrome	H01460	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ウエスト症候群	West syndrome	https://identifiers.org/kegg.disease:H01460
NANDO:1200592	http://nanbyodata.jp/ontology/NANDO_1200592	ウエスト症候群	West syndrome	H01460	http://www.geneontology.org/formats/oboInOwl#hasDbXref	点頭てんかん	West syndrome	https://identifiers.org/kegg.disease:H01460
NANDO:1200593	http://nanbyodata.jp/ontology/NANDO_1200593	大田原症候群	Ohtahara syndrome	H00606	http://www.geneontology.org/formats/oboInOwl#hasDbXref	大田原症候群	Ohtahara syndrome	https://identifiers.org/kegg.disease:H00606
NANDO:1200593	http://nanbyodata.jp/ontology/NANDO_1200593	大田原症候群	Ohtahara syndrome	H00606	http://www.geneontology.org/formats/oboInOwl#hasDbXref	早期乳児てんかん性脳症	Ohtahara syndrome	https://identifiers.org/kegg.disease:H00606
NANDO:1200593	http://nanbyodata.jp/ontology/NANDO_1200593	大田原症候群	Ohtahara syndrome	H00606	http://www.geneontology.org/formats/oboInOwl#hasDbXref	発達性およびてんかん性脳症	Ohtahara syndrome	https://identifiers.org/kegg.disease:H00606
NANDO:1200593	http://nanbyodata.jp/ontology/NANDO_1200593	大田原症候群	Ohtahara syndrome	H00606	http://www.geneontology.org/formats/oboInOwl#hasDbXref	大田原症候群	Developmental and epileptic encephalopathy	https://identifiers.org/kegg.disease:H00606
NANDO:1200593	http://nanbyodata.jp/ontology/NANDO_1200593	大田原症候群	Ohtahara syndrome	H00606	http://www.geneontology.org/formats/oboInOwl#hasDbXref	早期乳児てんかん性脳症	Developmental and epileptic encephalopathy	https://identifiers.org/kegg.disease:H00606
NANDO:1200593	http://nanbyodata.jp/ontology/NANDO_1200593	大田原症候群	Ohtahara syndrome	H00606	http://www.geneontology.org/formats/oboInOwl#hasDbXref	発達性およびてんかん性脳症	Developmental and epileptic encephalopathy	https://identifiers.org/kegg.disease:H00606
NANDO:1200593	http://nanbyodata.jp/ontology/NANDO_1200593	大田原症候群	Ohtahara syndrome	H00606	http://www.geneontology.org/formats/oboInOwl#hasDbXref	大田原症候群	Early infantile epileptic encephalopathy	https://identifiers.org/kegg.disease:H00606
NANDO:1200593	http://nanbyodata.jp/ontology/NANDO_1200593	大田原症候群	Ohtahara syndrome	H00606	http://www.geneontology.org/formats/oboInOwl#hasDbXref	早期乳児てんかん性脳症	Early infantile epileptic encephalopathy	https://identifiers.org/kegg.disease:H00606
NANDO:1200593	http://nanbyodata.jp/ontology/NANDO_1200593	大田原症候群	Ohtahara syndrome	H00606	http://www.geneontology.org/formats/oboInOwl#hasDbXref	発達性およびてんかん性脳症	Early infantile epileptic encephalopathy	https://identifiers.org/kegg.disease:H00606
NANDO:1200602	http://nanbyodata.jp/ontology/NANDO_1200602	ランドウ・クレフナー症候群	Landau-Kleffner syndrome	H01514	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ランドウ・クレフナー症候群	Landau-Kleffner syndrome	https://identifiers.org/kegg.disease:H01514
NANDO:1200603	http://nanbyodata.jp/ontology/NANDO_1200603	レット症候群	Rett syndrome	H00440	http://www.geneontology.org/formats/oboInOwl#hasDbXref	レット症候群	Rett syndrome	https://identifiers.org/kegg.disease:H00440
NANDO:1200607	http://nanbyodata.jp/ontology/NANDO_1200607	結節性硬化症	Tuberous sclerosis complex	H00915	http://www.geneontology.org/formats/oboInOwl#hasDbXref	結節性硬化症	Tuberous sclerosis complex	https://identifiers.org/kegg.disease:H00915
NANDO:1200607	http://nanbyodata.jp/ontology/NANDO_1200607	結節性硬化症	Tuberous sclerosis complex	H00915	http://www.geneontology.org/formats/oboInOwl#hasDbXref	結節性硬化症	Bourneville-Pringle disease	https://identifiers.org/kegg.disease:H00915
NANDO:1200608	http://nanbyodata.jp/ontology/NANDO_1200608	色素性乾皮症	Xeroderma pigmentosum	H01428	http://www.geneontology.org/formats/oboInOwl#hasDbXref	色素性乾皮症	Xeroderma pigmentosum	https://identifiers.org/kegg.disease:H01428
NANDO:1200614	http://nanbyodata.jp/ontology/NANDO_1200614	道化師様魚鱗癬	Harlequin ichthyosis	H00733	http://www.geneontology.org/formats/oboInOwl#hasDbXref	道化師様魚鱗癬	Harlequin ichthyosis	https://identifiers.org/kegg.disease:H00733
NANDO:1200620	http://nanbyodata.jp/ontology/NANDO_1200620	シェーグレン・ラルソン症候群	Sjögren-Larsson syndrome	H00162	http://www.geneontology.org/formats/oboInOwl#hasDbXref	シェーグレン・ラルソン症候群	Sjogren-Larsson syndrome	https://identifiers.org/kegg.disease:H00162
NANDO:1200622	http://nanbyodata.jp/ontology/NANDO_1200622	ドルフマン・シャナリン症候群	Dorfman-Chanarin syndrome	H00736	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ドルフマン・シャナリン症候群	Dorfman-Chanarin syndrome	https://identifiers.org/kegg.disease:H00736
NANDO:1200622	http://nanbyodata.jp/ontology/NANDO_1200622	ドルフマン・シャナリン症候群	Dorfman-Chanarin syndrome	H00736	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ドルフマン・シャナリン症候群	Chanarin-Dorfman syndrome	https://identifiers.org/kegg.disease:H00736
NANDO:1200631	http://nanbyodata.jp/ontology/NANDO_1200631	家族性良性慢性天疱瘡	Benign familial pemphigus	H00844	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ヘイリー・ヘイリー病	Familial benign chronic pemphigus	https://identifiers.org/kegg.disease:H00844
NANDO:1200631	http://nanbyodata.jp/ontology/NANDO_1200631	家族性良性慢性天疱瘡	Benign familial pemphigus	H00844	http://www.geneontology.org/formats/oboInOwl#hasDbXref	家族性良性慢性天疱瘡	Familial benign chronic pemphigus	https://identifiers.org/kegg.disease:H00844
NANDO:1200631	http://nanbyodata.jp/ontology/NANDO_1200631	家族性良性慢性天疱瘡	Benign familial pemphigus	H00844	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ヘイリー・ヘイリー病	Hailey-Hailey disease	https://identifiers.org/kegg.disease:H00844
NANDO:1200631	http://nanbyodata.jp/ontology/NANDO_1200631	家族性良性慢性天疱瘡	Benign familial pemphigus	H00844	http://www.geneontology.org/formats/oboInOwl#hasDbXref	家族性良性慢性天疱瘡	Hailey-Hailey disease	https://identifiers.org/kegg.disease:H00844
NANDO:1200632	http://nanbyodata.jp/ontology/NANDO_1200632	類天疱瘡	Pemphigoid (including Epidermolysis bullosa acquisita)	H01650	http://www.geneontology.org/formats/oboInOwl#hasDbXref	類天疱瘡	Pemphigoid	https://identifiers.org/kegg.disease:H01650
NANDO:1200637	http://nanbyodata.jp/ontology/NANDO_1200637	眼皮膚白皮症	Oculocutaneous albinism	H00168	http://www.geneontology.org/formats/oboInOwl#hasDbXref	眼皮膚白皮症	Oculocutaneous albinism	https://identifiers.org/kegg.disease:H00168
NANDO:1200638	http://nanbyodata.jp/ontology/NANDO_1200638	ヘルマンスキー・パドラック症候群	Hermansky-Pudlak syndrome	H00166	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ヘルマンスキー・パドラック症候群	Hermansky-Pudlak syndrome	https://identifiers.org/kegg.disease:H00166
NANDO:1200643	http://nanbyodata.jp/ontology/NANDO_1200643	弾性線維性仮性黄色腫	Pseudoxanthoma elasticum	H00560	http://www.geneontology.org/formats/oboInOwl#hasDbXref	弾性線維性仮性黄色腫	Pseudoxanthoma elasticum	https://identifiers.org/kegg.disease:H00560
NANDO:1200645	http://nanbyodata.jp/ontology/NANDO_1200645	エーラス・ダンロス症候群	Ehlers-Danlos Syndrome	H00802	http://www.geneontology.org/formats/oboInOwl#hasDbXref	エーラス・ダンロス症候群	Ehlers-Danlos syndrome	https://identifiers.org/kegg.disease:H00802
NANDO:1200655	http://nanbyodata.jp/ontology/NANDO_1200655	ウィルソン病	Wilson disease	H00210	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ウィルソン病	Wilson disease	https://identifiers.org/kegg.disease:H00210
NANDO:1200655	http://nanbyodata.jp/ontology/NANDO_1200655	ウィルソン病	Wilson disease	H00210	http://www.geneontology.org/formats/oboInOwl#hasDbXref	肝レンズ核変性症	Wilson disease	https://identifiers.org/kegg.disease:H00210
NANDO:1200655	http://nanbyodata.jp/ontology/NANDO_1200655	ウィルソン病	Wilson disease	H00210	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ウィルソン病	Hepatolenticular degeneration	https://identifiers.org/kegg.disease:H00210
NANDO:1200655	http://nanbyodata.jp/ontology/NANDO_1200655	ウィルソン病	Wilson disease	H00210	http://www.geneontology.org/formats/oboInOwl#hasDbXref	肝レンズ核変性症	Hepatolenticular degeneration	https://identifiers.org/kegg.disease:H00210
NANDO:1200656	http://nanbyodata.jp/ontology/NANDO_1200656	低ホスファターゼ症	Hypophosphatasia	H00213	http://www.geneontology.org/formats/oboInOwl#hasDbXref	低ホスファターゼ症	Hypophosphatasia	https://identifiers.org/kegg.disease:H00213
NANDO:1200658	http://nanbyodata.jp/ontology/NANDO_1200658	那須・ハコラ病	Nasu-Hakola disease	H00438	http://www.geneontology.org/formats/oboInOwl#hasDbXref	多発性骨嚢胞および白質脳症	Nasu-Hakola disease	https://identifiers.org/kegg.disease:H00438
NANDO:1200658	http://nanbyodata.jp/ontology/NANDO_1200658	那須・ハコラ病	Nasu-Hakola disease	H00438	http://www.geneontology.org/formats/oboInOwl#hasDbXref	那須ハコラ病	Nasu-Hakola disease	https://identifiers.org/kegg.disease:H00438
NANDO:1200658	http://nanbyodata.jp/ontology/NANDO_1200658	那須・ハコラ病	Nasu-Hakola disease	H00438	http://www.geneontology.org/formats/oboInOwl#hasDbXref	多発性骨嚢胞および白質脳症	Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy	https://identifiers.org/kegg.disease:H00438
NANDO:1200658	http://nanbyodata.jp/ontology/NANDO_1200658	那須・ハコラ病	Nasu-Hakola disease	H00438	http://www.geneontology.org/formats/oboInOwl#hasDbXref	那須ハコラ病	Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy	https://identifiers.org/kegg.disease:H00438
NANDO:1200660	http://nanbyodata.jp/ontology/NANDO_1200660	コフィン・ローリー症候群	Coffin-Lowry syndrome	H00574	http://www.geneontology.org/formats/oboInOwl#hasDbXref	コフィン・ローリー症候群	Coffin-Lowry syndrome	https://identifiers.org/kegg.disease:H00574
NANDO:1200661	http://nanbyodata.jp/ontology/NANDO_1200661	ジュベール症候群関連疾患	Joubert syndrome and related disorders	H00530	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ジュベール症候群関連疾患	Joubert syndrome and related disorders	https://identifiers.org/kegg.disease:H00530
NANDO:1200663	http://nanbyodata.jp/ontology/NANDO_1200663	モワット・ウィルソン症候群	Mowat-Wilson syndrome	H00908	http://www.geneontology.org/formats/oboInOwl#hasDbXref	モワットウィルソン症候群	Mowat-Wilson syndrome	https://identifiers.org/kegg.disease:H00908
NANDO:1200664	http://nanbyodata.jp/ontology/NANDO_1200664	ウィリアムズ症候群	Williams syndrome	H01439	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ウィリアムズ症候群	Williams-Beuren syndrome	https://identifiers.org/kegg.disease:H01439
NANDO:1200670	http://nanbyodata.jp/ontology/NANDO_1200670	コフィン・シリス症候群	Coffin-Siris syndrome	H01403	http://www.geneontology.org/formats/oboInOwl#hasDbXref	コフィン・シリス症候群	Coffin-Siris syndrome	https://identifiers.org/kegg.disease:H01403
NANDO:1200672	http://nanbyodata.jp/ontology/NANDO_1200672	歌舞伎症候群	Kabuki syndrome	H00570	http://www.geneontology.org/formats/oboInOwl#hasDbXref	歌舞伎症候群	Kabuki syndrome	https://identifiers.org/kegg.disease:H00570
NANDO:1200677	http://nanbyodata.jp/ontology/NANDO_1200677	コケイン症候群	Cockayne syndrome	H00076	http://www.geneontology.org/formats/oboInOwl#hasDbXref	コケイン症候群	Cockayne syndrome	https://identifiers.org/kegg.disease:H00076
NANDO:1200678	http://nanbyodata.jp/ontology/NANDO_1200678	プラダー・ウィリ症候群	Prader-Willi syndrome	H00478	http://www.geneontology.org/formats/oboInOwl#hasDbXref	プラダー・ウィリー症候群	Prader-Willi syndrome	https://identifiers.org/kegg.disease:H00478
NANDO:1200679	http://nanbyodata.jp/ontology/NANDO_1200679	ソトス症候群	Sotos syndrome	H00718	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ソトス症候群	Sotos syndrome	https://identifiers.org/kegg.disease:H00718
NANDO:1200684	http://nanbyodata.jp/ontology/NANDO_1200684	5p欠失症候群	5p deletion syndrome	H00764	http://www.geneontology.org/formats/oboInOwl#hasDbXref	5p欠失症候群	Cri du chat syndrome	https://identifiers.org/kegg.disease:H00764
NANDO:1200684	http://nanbyodata.jp/ontology/NANDO_1200684	5p欠失症候群	5p deletion syndrome	H00764	http://www.geneontology.org/formats/oboInOwl#hasDbXref	猫鳴き症候群	Cri du chat syndrome	https://identifiers.org/kegg.disease:H00764
NANDO:1200684	http://nanbyodata.jp/ontology/NANDO_1200684	5p欠失症候群	5p deletion syndrome	H00764	http://www.geneontology.org/formats/oboInOwl#hasDbXref	5p欠失症候群	Cat cry syndrome	https://identifiers.org/kegg.disease:H00764
NANDO:1200684	http://nanbyodata.jp/ontology/NANDO_1200684	5p欠失症候群	5p deletion syndrome	H00764	http://www.geneontology.org/formats/oboInOwl#hasDbXref	猫鳴き症候群	Cat cry syndrome	https://identifiers.org/kegg.disease:H00764
NANDO:1200684	http://nanbyodata.jp/ontology/NANDO_1200684	5p欠失症候群	5p deletion syndrome	H00764	http://www.geneontology.org/formats/oboInOwl#hasDbXref	5p欠失症候群	Chromosome 5p deletion syndrome	https://identifiers.org/kegg.disease:H00764
NANDO:1200684	http://nanbyodata.jp/ontology/NANDO_1200684	5p欠失症候群	5p deletion syndrome	H00764	http://www.geneontology.org/formats/oboInOwl#hasDbXref	猫鳴き症候群	Chromosome 5p deletion syndrome	https://identifiers.org/kegg.disease:H00764
NANDO:1200688	http://nanbyodata.jp/ontology/NANDO_1200688	22q11.2欠失症候群	22q11.2 deletion syndrome	H01525	http://www.geneontology.org/formats/oboInOwl#hasDbXref	22q11.2 欠失症候群	22q11.2 deletion syndrome	https://identifiers.org/kegg.disease:H01525
NANDO:1200688	http://nanbyodata.jp/ontology/NANDO_1200688	22q11.2欠失症候群	22q11.2 deletion syndrome	H01525	http://www.geneontology.org/formats/oboInOwl#hasDbXref	キャッチ 22	22q11.2 deletion syndrome	https://identifiers.org/kegg.disease:H01525
NANDO:1200688	http://nanbyodata.jp/ontology/NANDO_1200688	22q11.2欠失症候群	22q11.2 deletion syndrome	H01525	http://www.geneontology.org/formats/oboInOwl#hasDbXref	22q11.2 欠失症候群	CATCH22	https://identifiers.org/kegg.disease:H01525
NANDO:1200688	http://nanbyodata.jp/ontology/NANDO_1200688	22q11.2欠失症候群	22q11.2 deletion syndrome	H01525	http://www.geneontology.org/formats/oboInOwl#hasDbXref	キャッチ 22	CATCH22	https://identifiers.org/kegg.disease:H01525
NANDO:1200692	http://nanbyodata.jp/ontology/NANDO_1200692	脆弱X症候群	Fragile X syndrome	H00465	http://www.geneontology.org/formats/oboInOwl#hasDbXref	脆弱Ｘ症候群	Fragile X syndrome	https://identifiers.org/kegg.disease:H00465
NANDO:1200699	http://nanbyodata.jp/ontology/NANDO_1200699	完全大血管転位症	Complete transposition of the great arteries	H00550	http://www.geneontology.org/formats/oboInOwl#hasDbXref	完全大血管転位症	Complete transposition of the great arteries	https://identifiers.org/kegg.disease:H00550
NANDO:1200705	http://nanbyodata.jp/ontology/NANDO_1200705	左心低形成症候群	Hypoplastic left heart syndrome	H01272	http://www.geneontology.org/formats/oboInOwl#hasDbXref	左心低形成症候群	Hypoplastic left heart syndrome	https://identifiers.org/kegg.disease:H01272
NANDO:1200709	http://nanbyodata.jp/ontology/NANDO_1200709	ファロー四徴症	Tetralogy of Fallot	H00549	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ファロー四徴症	Tetralogy of Fallot	https://identifiers.org/kegg.disease:H00549
NANDO:1200710	http://nanbyodata.jp/ontology/NANDO_1200710	両大血管右室起始症	Double outlet right ventricle	H00918	http://www.geneontology.org/formats/oboInOwl#hasDbXref	両大血管右室起始症	Double-outlet right ventricle	https://identifiers.org/kegg.disease:H00918
NANDO:1200712	http://nanbyodata.jp/ontology/NANDO_1200712	アルポート症候群	Alport's syndrome	H00581	http://www.geneontology.org/formats/oboInOwl#hasDbXref	アルポート症候群	Alport syndrome	https://identifiers.org/kegg.disease:H00581
NANDO:1200714	http://nanbyodata.jp/ontology/NANDO_1200714	急速進行性糸球体腎炎	Rapidly progressive glomerulonephritis	H01688	http://www.geneontology.org/formats/oboInOwl#hasDbXref	急速進行性糸球体腎炎	Rapidly progressive glomerulonephritis	https://identifiers.org/kegg.disease:H01688
NANDO:1200722	http://nanbyodata.jp/ontology/NANDO_1200722	巣状分節性糸球体硬化症	Focal segmental glomerulosclerosis	H00626	http://www.geneontology.org/formats/oboInOwl#hasDbXref	巣状分節性糸球体硬化症	Focal segmental glomerulosclerosis	https://identifiers.org/kegg.disease:H00626
NANDO:1200742	http://nanbyodata.jp/ontology/NANDO_1200742	先天性腎性尿崩症	Congenital nephrogenic diabetes insipidus	H00252	http://www.geneontology.org/formats/oboInOwl#hasDbXref	先天性腎性尿崩症	Congenital nephrogenic diabetes insipidus	https://identifiers.org/kegg.disease:H00252
NANDO:1200744	http://nanbyodata.jp/ontology/NANDO_1200744	オスラー病	Osler disease	H00533	http://www.geneontology.org/formats/oboInOwl#hasDbXref	オスラー病	Hereditary hemorrhagic telangiectasia	https://identifiers.org/kegg.disease:H00533
NANDO:1200744	http://nanbyodata.jp/ontology/NANDO_1200744	オスラー病	Osler disease	H00533	http://www.geneontology.org/formats/oboInOwl#hasDbXref	遺伝性出血性毛細血管拡張症	Hereditary hemorrhagic telangiectasia	https://identifiers.org/kegg.disease:H00533
NANDO:1200744	http://nanbyodata.jp/ontology/NANDO_1200744	オスラー病	Osler disease	H00533	http://www.geneontology.org/formats/oboInOwl#hasDbXref	オスラー病	Osler disease	https://identifiers.org/kegg.disease:H00533
NANDO:1200744	http://nanbyodata.jp/ontology/NANDO_1200744	オスラー病	Osler disease	H00533	http://www.geneontology.org/formats/oboInOwl#hasDbXref	遺伝性出血性毛細血管拡張症	Osler disease	https://identifiers.org/kegg.disease:H00533
NANDO:1200746	http://nanbyodata.jp/ontology/NANDO_1200746	肺胞蛋白症	Pulmonary alveolar proteinosis	H00217	http://www.geneontology.org/formats/oboInOwl#hasDbXref	肺胞蛋白症	Pulmonary alveolar proteinosis	https://identifiers.org/kegg.disease:H00217
NANDO:1200750	http://nanbyodata.jp/ontology/NANDO_1200750	先天性肺胞蛋白症	Congenital alveolar proteinosis	H01122	http://www.geneontology.org/formats/oboInOwl#hasDbXref	先天性肺胞蛋白症	Congenital pulmonary alveolar proteinosis	https://identifiers.org/kegg.disease:H01122
NANDO:1200750	http://nanbyodata.jp/ontology/NANDO_1200750	先天性肺胞蛋白症	Congenital alveolar proteinosis	H01122	http://www.geneontology.org/formats/oboInOwl#hasDbXref	肺サーファクタント代謝異常症	Congenital pulmonary alveolar proteinosis	https://identifiers.org/kegg.disease:H01122
NANDO:1200750	http://nanbyodata.jp/ontology/NANDO_1200750	先天性肺胞蛋白症	Congenital alveolar proteinosis	H01122	http://www.geneontology.org/formats/oboInOwl#hasDbXref	先天性肺胞蛋白症	Pulmonary surfactant metabolism dysfunction	https://identifiers.org/kegg.disease:H01122
NANDO:1200750	http://nanbyodata.jp/ontology/NANDO_1200750	先天性肺胞蛋白症	Congenital alveolar proteinosis	H01122	http://www.geneontology.org/formats/oboInOwl#hasDbXref	肺サーファクタント代謝異常症	Pulmonary surfactant metabolism dysfunction	https://identifiers.org/kegg.disease:H01122
NANDO:1200753	http://nanbyodata.jp/ontology/NANDO_1200753	先天性中枢性低換気症候群	Congenital central hypoventilation syndrome	H00916	http://www.geneontology.org/formats/oboInOwl#hasDbXref	先天性中枢性低換気症候群	Congenital central hypoventilation syndrome	https://identifiers.org/kegg.disease:H00916
NANDO:1200755	http://nanbyodata.jp/ontology/NANDO_1200755	α1-アンチトリプシン欠損症	Alpha-1-antitrypsin deficiency	H01103	http://www.geneontology.org/formats/oboInOwl#hasDbXref	α1-アンチトリプシン欠乏症	Alpha-1-antitrypsin deficiency	https://identifiers.org/kegg.disease:H01103
NANDO:1200757	http://nanbyodata.jp/ontology/NANDO_1200757	ウォルフラム症候群	Wolfram syndrome	H00854	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ウォルフラム症候群	Wolfram syndrome	https://identifiers.org/kegg.disease:H00854
NANDO:1200757	http://nanbyodata.jp/ontology/NANDO_1200757	ウォルフラム症候群	Wolfram syndrome	H00854	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ウォルフラム症候群	DIDMOAD syndrome	https://identifiers.org/kegg.disease:H00854
NANDO:1200759	http://nanbyodata.jp/ontology/NANDO_1200759	ペルオキシソーム形成異常症	Peroxisome biogenesis disorders	H00205	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ペルオキシソーム形成異常症	Peroxisome biogenesis disorder	https://identifiers.org/kegg.disease:H00205
NANDO:1200760	http://nanbyodata.jp/ontology/NANDO_1200760	ツェルベーガー症候群	Zellweger syndrome	H01342	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ツェルウエーガー症候群	Zellweger syndrome	https://identifiers.org/kegg.disease:H01342
NANDO:1200761	http://nanbyodata.jp/ontology/NANDO_1200761	新生児型副腎白質ジストロフィー	Neonatal adrenoleukodystrophy	H00177	http://www.geneontology.org/formats/oboInOwl#hasDbXref	新生児型副腎白質ジストロフィー	Neonatal adrenoleukodystrophy	https://identifiers.org/kegg.disease:H00177
NANDO:1200764	http://nanbyodata.jp/ontology/NANDO_1200764	ペルオキシソームβ酸化系酵素欠損症	Peroxisomal beta-oxidation enzyme deficiency	H00407	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ペルオキシソームβ酸化系酵素欠損症	Peroxisomal beta-oxidation enzyme deficiency	https://identifiers.org/kegg.disease:H00407
NANDO:1200769	http://nanbyodata.jp/ontology/NANDO_1200769	レフサム病	Refsum disease	H00075	http://www.geneontology.org/formats/oboInOwl#hasDbXref	レフスム病	Refsum disease	https://identifiers.org/kegg.disease:H00075
NANDO:1200769	http://nanbyodata.jp/ontology/NANDO_1200769	レフサム病	Refsum disease	H00075	http://www.geneontology.org/formats/oboInOwl#hasDbXref	多発神経炎型遺伝性失調症	Refsum disease	https://identifiers.org/kegg.disease:H00075
NANDO:1200769	http://nanbyodata.jp/ontology/NANDO_1200769	レフサム病	Refsum disease	H00075	http://www.geneontology.org/formats/oboInOwl#hasDbXref	レフスム病	Heredopathia atactica polyneuritiformis	https://identifiers.org/kegg.disease:H00075
NANDO:1200769	http://nanbyodata.jp/ontology/NANDO_1200769	レフサム病	Refsum disease	H00075	http://www.geneontology.org/formats/oboInOwl#hasDbXref	多発神経炎型遺伝性失調症	Heredopathia atactica polyneuritiformis	https://identifiers.org/kegg.disease:H00075
NANDO:1200774	http://nanbyodata.jp/ontology/NANDO_1200774	アカタラセミア	Acatalasemia	H00203	http://www.geneontology.org/formats/oboInOwl#hasDbXref	無カタラーゼ血症	Acatalasemia	https://identifiers.org/kegg.disease:H00203
NANDO:1200774	http://nanbyodata.jp/ontology/NANDO_1200774	アカタラセミア	Acatalasemia	H00203	http://www.geneontology.org/formats/oboInOwl#hasDbXref	高原病	Acatalasemia	https://identifiers.org/kegg.disease:H00203
NANDO:1200774	http://nanbyodata.jp/ontology/NANDO_1200774	アカタラセミア	Acatalasemia	H00203	http://www.geneontology.org/formats/oboInOwl#hasDbXref	無カタラーゼ血症	Takahara disease	https://identifiers.org/kegg.disease:H00203
NANDO:1200774	http://nanbyodata.jp/ontology/NANDO_1200774	アカタラセミア	Acatalasemia	H00203	http://www.geneontology.org/formats/oboInOwl#hasDbXref	高原病	Takahara disease	https://identifiers.org/kegg.disease:H00203
NANDO:1200776	http://nanbyodata.jp/ontology/NANDO_1200776	偽性副甲状腺機能低下症	Pseudohypoparathyroidism	H00244	http://www.geneontology.org/formats/oboInOwl#hasDbXref	偽性副甲状腺機能低下症	Pseudohypoparathyroidism	https://identifiers.org/kegg.disease:H00244
NANDO:1200777	http://nanbyodata.jp/ontology/NANDO_1200777	副腎皮質刺激ホルモン不応症	ACTH unresponsiveness	H00256	http://www.geneontology.org/formats/oboInOwl#hasDbXref	副腎皮質刺激ホルモン不応症	Familial glucocorticoid deficiency	https://identifiers.org/kegg.disease:H00256
NANDO:1200777	http://nanbyodata.jp/ontology/NANDO_1200777	副腎皮質刺激ホルモン不応症	ACTH unresponsiveness	H00256	http://www.geneontology.org/formats/oboInOwl#hasDbXref	家族性糖質コルチコイド欠損症	Familial glucocorticoid deficiency	https://identifiers.org/kegg.disease:H00256
NANDO:1200784	http://nanbyodata.jp/ontology/NANDO_1200784	フェニルケトン尿症	Phenylketonuria	H00167	http://www.geneontology.org/formats/oboInOwl#hasDbXref	フェニルケトン尿症	Hyperphenylalaninemia	https://identifiers.org/kegg.disease:H00167
NANDO:1200784	http://nanbyodata.jp/ontology/NANDO_1200784	フェニルケトン尿症	Phenylketonuria	H00167	http://www.geneontology.org/formats/oboInOwl#hasDbXref	高フェニルアラニン血症	Hyperphenylalaninemia	https://identifiers.org/kegg.disease:H00167
NANDO:1200784	http://nanbyodata.jp/ontology/NANDO_1200784	フェニルケトン尿症	Phenylketonuria	H00167	http://www.geneontology.org/formats/oboInOwl#hasDbXref	フェニルケトン尿症	Phenylketonuria	https://identifiers.org/kegg.disease:H00167
NANDO:1200784	http://nanbyodata.jp/ontology/NANDO_1200784	フェニルケトン尿症	Phenylketonuria	H00167	http://www.geneontology.org/formats/oboInOwl#hasDbXref	高フェニルアラニン血症	Phenylketonuria	https://identifiers.org/kegg.disease:H00167
NANDO:1200791	http://nanbyodata.jp/ontology/NANDO_1200791	メープルシロップ尿症	Maple syrup urine disease	H00172	http://www.geneontology.org/formats/oboInOwl#hasDbXref	メープルシロップ尿症	Maple syrup urine disease	https://identifiers.org/kegg.disease:H00172
NANDO:1200792	http://nanbyodata.jp/ontology/NANDO_1200792	プロピオン酸血症	Propionic acidemia	H00175	http://www.geneontology.org/formats/oboInOwl#hasDbXref	プロピオン酸血症	Propionic acidemia	https://identifiers.org/kegg.disease:H00175
NANDO:1200793	http://nanbyodata.jp/ontology/NANDO_1200793	メチルマロン酸血症	Methylmalonic acidemia	H00174	http://www.geneontology.org/formats/oboInOwl#hasDbXref	メチルマロン酸血症	Methylmalonic acidemia	https://identifiers.org/kegg.disease:H00174
NANDO:1200793	http://nanbyodata.jp/ontology/NANDO_1200793	メチルマロン酸血症	Methylmalonic acidemia	H00174	http://www.geneontology.org/formats/oboInOwl#hasDbXref	メチルマロン酸尿症	Methylmalonic acidemia	https://identifiers.org/kegg.disease:H00174
NANDO:1200793	http://nanbyodata.jp/ontology/NANDO_1200793	メチルマロン酸血症	Methylmalonic acidemia	H00174	http://www.geneontology.org/formats/oboInOwl#hasDbXref	メチルマロン酸血症	Methylmalonic aciduria	https://identifiers.org/kegg.disease:H00174
NANDO:1200793	http://nanbyodata.jp/ontology/NANDO_1200793	メチルマロン酸血症	Methylmalonic acidemia	H00174	http://www.geneontology.org/formats/oboInOwl#hasDbXref	メチルマロン酸尿症	Methylmalonic aciduria	https://identifiers.org/kegg.disease:H00174
NANDO:1200798	http://nanbyodata.jp/ontology/NANDO_1200798	イソ吉草酸血症	Isovaleric acidemia	H00173	http://www.geneontology.org/formats/oboInOwl#hasDbXref	イソ吉草酸血症	Isovaleric acidemia	https://identifiers.org/kegg.disease:H00173
NANDO:1200799	http://nanbyodata.jp/ontology/NANDO_1200799	グルコーストランスポーター1欠損症	Glucose transporter 1 deficiency	H00836	http://www.geneontology.org/formats/oboInOwl#hasDbXref	グルコーストランスポーター1欠損症	GLUT1 deficiency syndrome	https://identifiers.org/kegg.disease:H00836
NANDO:1200799	http://nanbyodata.jp/ontology/NANDO_1200799	グルコーストランスポーター1欠損症	Glucose transporter 1 deficiency	H00836	http://www.geneontology.org/formats/oboInOwl#hasDbXref	GLUT1欠損症候群	GLUT1 deficiency syndrome	https://identifiers.org/kegg.disease:H00836
NANDO:1200799	http://nanbyodata.jp/ontology/NANDO_1200799	グルコーストランスポーター1欠損症	Glucose transporter 1 deficiency	H00836	http://www.geneontology.org/formats/oboInOwl#hasDbXref	グルコーストランスポーター1欠損症	Glucose transport defect of the blood-brain barrier	https://identifiers.org/kegg.disease:H00836
NANDO:1200799	http://nanbyodata.jp/ontology/NANDO_1200799	グルコーストランスポーター1欠損症	Glucose transporter 1 deficiency	H00836	http://www.geneontology.org/formats/oboInOwl#hasDbXref	GLUT1欠損症候群	Glucose transport defect of the blood-brain barrier	https://identifiers.org/kegg.disease:H00836
NANDO:1200802	http://nanbyodata.jp/ontology/NANDO_1200802	尿素サイクル異常症	Urea cycle disorder	H01398	http://www.geneontology.org/formats/oboInOwl#hasDbXref	尿素サイクル異常症	Primary hyperammonemia (Urea cycle disorders)	https://identifiers.org/kegg.disease:H01398
NANDO:1200802	http://nanbyodata.jp/ontology/NANDO_1200802	尿素サイクル異常症	Urea cycle disorder	H01398	http://www.geneontology.org/formats/oboInOwl#hasDbXref	原発性高アンモニア血症	Primary hyperammonemia (Urea cycle disorders)	https://identifiers.org/kegg.disease:H01398
NANDO:1200804	http://nanbyodata.jp/ontology/NANDO_1200804	OTC欠損症	Ornithine transcarbamylase deficiency	H00187	http://www.geneontology.org/formats/oboInOwl#hasDbXref	オルニチントランスカルバミラーゼ欠損症	Ornithine transcarbamylase deficiency	https://identifiers.org/kegg.disease:H00187
NANDO:1200806	http://nanbyodata.jp/ontology/NANDO_1200806	アルギニノコハク酸尿症	Argininosuccinic aciduria	H01028	http://www.geneontology.org/formats/oboInOwl#hasDbXref	アルギニノコハク酸尿症	Argininosuccinic aciduria	https://identifiers.org/kegg.disease:H01028
NANDO:1200806	http://nanbyodata.jp/ontology/NANDO_1200806	アルギニノコハク酸尿症	Argininosuccinic aciduria	H01028	http://www.geneontology.org/formats/oboInOwl#hasDbXref	アルギニノコハク酸分解酵素欠損症	Argininosuccinic aciduria	https://identifiers.org/kegg.disease:H01028
NANDO:1200806	http://nanbyodata.jp/ontology/NANDO_1200806	アルギニノコハク酸尿症	Argininosuccinic aciduria	H01028	http://www.geneontology.org/formats/oboInOwl#hasDbXref	アルギニノコハク酸尿症	Argininosuccinate lyase deficiency	https://identifiers.org/kegg.disease:H01028
NANDO:1200806	http://nanbyodata.jp/ontology/NANDO_1200806	アルギニノコハク酸尿症	Argininosuccinic aciduria	H01028	http://www.geneontology.org/formats/oboInOwl#hasDbXref	アルギニノコハク酸分解酵素欠損症	Argininosuccinate lyase deficiency	https://identifiers.org/kegg.disease:H01028
NANDO:1200808	http://nanbyodata.jp/ontology/NANDO_1200808	NAGS欠損症	NAGS deficiency	H01032	http://www.geneontology.org/formats/oboInOwl#hasDbXref	NAGS欠損症	N-acetylglutamate synthase deficiency	https://identifiers.org/kegg.disease:H01032
NANDO:1200808	http://nanbyodata.jp/ontology/NANDO_1200808	NAGS欠損症	NAGS deficiency	H01032	http://www.geneontology.org/formats/oboInOwl#hasDbXref	N-アセチルグルタミン酸合成酵素欠損症	N-acetylglutamate synthase deficiency	https://identifiers.org/kegg.disease:H01032
NANDO:1200809	http://nanbyodata.jp/ontology/NANDO_1200809	リジン尿性蛋白不耐症	Lysinuric protein intolerance	H00899	http://www.geneontology.org/formats/oboInOwl#hasDbXref	リジン尿性蛋白不耐症	Lysinuric protein intolerance	https://identifiers.org/kegg.disease:H00899
NANDO:1200810	http://nanbyodata.jp/ontology/NANDO_1200810	先天性葉酸吸収不全症	Hereditary folate malabsorption	H01252	http://www.geneontology.org/formats/oboInOwl#hasDbXref	先天性葉酸吸収不全	Hereditary folate malabsorption	https://identifiers.org/kegg.disease:H01252
NANDO:1200820	http://nanbyodata.jp/ontology/NANDO_1200820	複合カルボキシラーゼ欠損症	Multiple carboxylase deficiency	H00180	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ホロカルボキシラーゼ合成酵素欠損症	Holocarboxylase synthetase deficiency	https://identifiers.org/kegg.disease:H00180
NANDO:1200820	http://nanbyodata.jp/ontology/NANDO_1200820	複合カルボキシラーゼ欠損症	Multiple carboxylase deficiency	H00180	http://www.geneontology.org/formats/oboInOwl#hasDbXref	複合カルボキシラーゼ欠損症	Holocarboxylase synthetase deficiency	https://identifiers.org/kegg.disease:H00180
NANDO:1200820	http://nanbyodata.jp/ontology/NANDO_1200820	複合カルボキシラーゼ欠損症	Multiple carboxylase deficiency	H00180	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ホロカルボキシラーゼ合成酵素欠損症	Multiple carboxylase deficiency	https://identifiers.org/kegg.disease:H00180
NANDO:1200820	http://nanbyodata.jp/ontology/NANDO_1200820	複合カルボキシラーゼ欠損症	Multiple carboxylase deficiency	H00180	http://www.geneontology.org/formats/oboInOwl#hasDbXref	複合カルボキシラーゼ欠損症	Multiple carboxylase deficiency	https://identifiers.org/kegg.disease:H00180
NANDO:1200821	http://nanbyodata.jp/ontology/NANDO_1200821	ホロカルボキシラーゼ合成酵素欠損症	Holocarboxylase synthetase deficiency	H00180	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ホロカルボキシラーゼ合成酵素欠損症	Holocarboxylase synthetase deficiency	https://identifiers.org/kegg.disease:H00180
NANDO:1200821	http://nanbyodata.jp/ontology/NANDO_1200821	ホロカルボキシラーゼ合成酵素欠損症	Holocarboxylase synthetase deficiency	H00180	http://www.geneontology.org/formats/oboInOwl#hasDbXref	複合カルボキシラーゼ欠損症	Holocarboxylase synthetase deficiency	https://identifiers.org/kegg.disease:H00180
NANDO:1200821	http://nanbyodata.jp/ontology/NANDO_1200821	ホロカルボキシラーゼ合成酵素欠損症	Holocarboxylase synthetase deficiency	H00180	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ホロカルボキシラーゼ合成酵素欠損症	Multiple carboxylase deficiency	https://identifiers.org/kegg.disease:H00180
NANDO:1200821	http://nanbyodata.jp/ontology/NANDO_1200821	ホロカルボキシラーゼ合成酵素欠損症	Holocarboxylase synthetase deficiency	H00180	http://www.geneontology.org/formats/oboInOwl#hasDbXref	複合カルボキシラーゼ欠損症	Multiple carboxylase deficiency	https://identifiers.org/kegg.disease:H00180
NANDO:1200822	http://nanbyodata.jp/ontology/NANDO_1200822	ビオチニダーゼ欠損症	Biotinidase deficiency	H01182	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ビオチニダーゼ欠損症	Biotinidase deficiency	https://identifiers.org/kegg.disease:H01182
NANDO:1200822	http://nanbyodata.jp/ontology/NANDO_1200822	ビオチニダーゼ欠損症	Biotinidase deficiency	H01182	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ビオチニダーゼ欠損症	Late-onset multiple carboxylase deficiency	https://identifiers.org/kegg.disease:H01182
NANDO:1200822	http://nanbyodata.jp/ontology/NANDO_1200822	ビオチニダーゼ欠損症	Biotinidase deficiency	H01182	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ビオチニダーゼ欠損症	BTD deficiency	https://identifiers.org/kegg.disease:H01182
NANDO:1200852	http://nanbyodata.jp/ontology/NANDO_1200852	レシチンコレステロールアシルトランスフェラーゼ欠損症	Lecithin cholesterol acyltransferase deficiency	H00158	http://www.geneontology.org/formats/oboInOwl#hasDbXref	レシチンコレステロールアシルトランスフェラーゼ欠損症	Norum disease	https://identifiers.org/kegg.disease:H00158
NANDO:1200852	http://nanbyodata.jp/ontology/NANDO_1200852	レシチンコレステロールアシルトランスフェラーゼ欠損症	Lecithin cholesterol acyltransferase deficiency	H00158	http://www.geneontology.org/formats/oboInOwl#hasDbXref	レシチンコレステロールアシルトランスフェラーゼ欠損症	Fish-eye disease	https://identifiers.org/kegg.disease:H00158
NANDO:1200852	http://nanbyodata.jp/ontology/NANDO_1200852	レシチンコレステロールアシルトランスフェラーゼ欠損症	Lecithin cholesterol acyltransferase deficiency	H00158	http://www.geneontology.org/formats/oboInOwl#hasDbXref	レシチンコレステロールアシルトランスフェラーゼ欠損症	Lecithin	https://identifiers.org/kegg.disease:H00158
NANDO:1200853	http://nanbyodata.jp/ontology/NANDO_1200853	シトステロール血症	Sitosterolemia	H00152	http://www.geneontology.org/formats/oboInOwl#hasDbXref	シトステロール血症	Sitosterolemia	https://identifiers.org/kegg.disease:H00152
NANDO:1200854	http://nanbyodata.jp/ontology/NANDO_1200854	タンジール病	Tangier disease	H00159	http://www.geneontology.org/formats/oboInOwl#hasDbXref	タンジール病	Tangier disease	https://identifiers.org/kegg.disease:H00159
NANDO:1200856	http://nanbyodata.jp/ontology/NANDO_1200856	脳腱黄色腫症	Cerebrotendinous xanthomatosis	H00151	http://www.geneontology.org/formats/oboInOwl#hasDbXref	脳腱黄色腫症	Cerebrotendinous xanthomatosis	https://identifiers.org/kegg.disease:H00151
NANDO:1200856	http://nanbyodata.jp/ontology/NANDO_1200856	脳腱黄色腫症	Cerebrotendinous xanthomatosis	H00151	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ヴァン-ボガエール病	Cerebrotendinous xanthomatosis	https://identifiers.org/kegg.disease:H00151
NANDO:1200856	http://nanbyodata.jp/ontology/NANDO_1200856	脳腱黄色腫症	Cerebrotendinous xanthomatosis	H00151	http://www.geneontology.org/formats/oboInOwl#hasDbXref	脳腱黄色腫症	Van Bogaert-Scherer-Epstein Disease	https://identifiers.org/kegg.disease:H00151
NANDO:1200856	http://nanbyodata.jp/ontology/NANDO_1200856	脳腱黄色腫症	Cerebrotendinous xanthomatosis	H00151	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ヴァン-ボガエール病	Van Bogaert-Scherer-Epstein Disease	https://identifiers.org/kegg.disease:H00151
NANDO:1200857	http://nanbyodata.jp/ontology/NANDO_1200857	無βリポタンパク血症	Abetalipoproteinemia	H00160	http://www.geneontology.org/formats/oboInOwl#hasDbXref	無βリポタンパク血症	Abetalipoproteinemia	https://identifiers.org/kegg.disease:H00160
NANDO:1200857	http://nanbyodata.jp/ontology/NANDO_1200857	無βリポタンパク血症	Abetalipoproteinemia	H00160	http://www.geneontology.org/formats/oboInOwl#hasDbXref	バッセン・コーンツヴァイク病	Abetalipoproteinemia	https://identifiers.org/kegg.disease:H00160
NANDO:1200857	http://nanbyodata.jp/ontology/NANDO_1200857	無βリポタンパク血症	Abetalipoproteinemia	H00160	http://www.geneontology.org/formats/oboInOwl#hasDbXref	無βリポタンパク血症	Bassen-Kornzweig Disease	https://identifiers.org/kegg.disease:H00160
NANDO:1200857	http://nanbyodata.jp/ontology/NANDO_1200857	無βリポタンパク血症	Abetalipoproteinemia	H00160	http://www.geneontology.org/formats/oboInOwl#hasDbXref	バッセン・コーンツヴァイク病	Bassen-Kornzweig Disease	https://identifiers.org/kegg.disease:H00160
NANDO:1200858	http://nanbyodata.jp/ontology/NANDO_1200858	脂肪萎縮症	Lipodystrophy	H01475	http://www.geneontology.org/formats/oboInOwl#hasDbXref	脂肪異栄養症	Lipodystrophy	https://identifiers.org/kegg.disease:H01475
NANDO:1200858	http://nanbyodata.jp/ontology/NANDO_1200858	脂肪萎縮症	Lipodystrophy	H01475	http://www.geneontology.org/formats/oboInOwl#hasDbXref	脂肪萎縮症	Lipodystrophy	https://identifiers.org/kegg.disease:H01475
NANDO:1200858	http://nanbyodata.jp/ontology/NANDO_1200858	脂肪萎縮症	Lipodystrophy	H01475	http://www.geneontology.org/formats/oboInOwl#hasDbXref	リポジストロフィー	Lipodystrophy	https://identifiers.org/kegg.disease:H01475
NANDO:1200858	http://nanbyodata.jp/ontology/NANDO_1200858	脂肪萎縮症	Lipodystrophy	H01475	http://www.geneontology.org/formats/oboInOwl#hasDbXref	脂肪異栄養症	Lipoatrophy	https://identifiers.org/kegg.disease:H01475
NANDO:1200858	http://nanbyodata.jp/ontology/NANDO_1200858	脂肪萎縮症	Lipodystrophy	H01475	http://www.geneontology.org/formats/oboInOwl#hasDbXref	脂肪萎縮症	Lipoatrophy	https://identifiers.org/kegg.disease:H01475
NANDO:1200858	http://nanbyodata.jp/ontology/NANDO_1200858	脂肪萎縮症	Lipodystrophy	H01475	http://www.geneontology.org/formats/oboInOwl#hasDbXref	リポジストロフィー	Lipoatrophy	https://identifiers.org/kegg.disease:H01475
NANDO:1200860	http://nanbyodata.jp/ontology/NANDO_1200860	後天性全身性脂肪萎縮症	Acquired generalized lipodystrophy	H01474	http://www.geneontology.org/formats/oboInOwl#hasDbXref	後天性全身性脂肪萎縮症	Acquired generalized lipodystrophy	https://identifiers.org/kegg.disease:H01474
NANDO:1200860	http://nanbyodata.jp/ontology/NANDO_1200860	後天性全身性脂肪萎縮症	Acquired generalized lipodystrophy	H01474	http://www.geneontology.org/formats/oboInOwl#hasDbXref	Lawrence 症候群	Acquired generalized lipodystrophy	https://identifiers.org/kegg.disease:H01474
NANDO:1200860	http://nanbyodata.jp/ontology/NANDO_1200860	後天性全身性脂肪萎縮症	Acquired generalized lipodystrophy	H01474	http://www.geneontology.org/formats/oboInOwl#hasDbXref	後天性全身性脂肪萎縮症	Lawrence syndrome	https://identifiers.org/kegg.disease:H01474
NANDO:1200860	http://nanbyodata.jp/ontology/NANDO_1200860	後天性全身性脂肪萎縮症	Acquired generalized lipodystrophy	H01474	http://www.geneontology.org/formats/oboInOwl#hasDbXref	Lawrence 症候群	Lawrence syndrome	https://identifiers.org/kegg.disease:H01474
NANDO:1200863	http://nanbyodata.jp/ontology/NANDO_1200863	家族性地中海熱	Familial Mediterranean fever	H00288	http://www.geneontology.org/formats/oboInOwl#hasDbXref	家族性地中海熱	Familial Mediterranean fever	https://identifiers.org/kegg.disease:H00288
NANDO:1200863	http://nanbyodata.jp/ontology/NANDO_1200863	家族性地中海熱	Familial Mediterranean fever	H00288	http://www.geneontology.org/formats/oboInOwl#hasDbXref	家族性地中海熱	Familial hereditary periodic fever syndromes	https://identifiers.org/kegg.disease:H00288
NANDO:1200868	http://nanbyodata.jp/ontology/NANDO_1200868	化膿性無菌性関節炎・壊疽性膿皮症・アクネ症候群	Pyogenic arthritis, pyoderma gangrenosum, acne syndrome	H00287	http://www.geneontology.org/formats/oboInOwl#hasDbXref	化膿性無菌性関節炎・壊疽性膿皮症・アクネ症候群	Pyogenic sterile arthritis, pyoderma gangrenosum, and acne syndrome	https://identifiers.org/kegg.disease:H00287
NANDO:1200869	http://nanbyodata.jp/ontology/NANDO_1200869	慢性再発性多発性骨髄炎	Chronic recurrent multifocal osteomyelitis	H01117	http://www.geneontology.org/formats/oboInOwl#hasDbXref	慢性再発性多発性骨髄炎	Chronic recurrent multifocal osteomyelitis	https://identifiers.org/kegg.disease:H01117
NANDO:1200869	http://nanbyodata.jp/ontology/NANDO_1200869	慢性再発性多発性骨髄炎	Chronic recurrent multifocal osteomyelitis	H01117	http://www.geneontology.org/formats/oboInOwl#hasDbXref	Majeed 症候群	Chronic recurrent multifocal osteomyelitis	https://identifiers.org/kegg.disease:H01117
NANDO:1200869	http://nanbyodata.jp/ontology/NANDO_1200869	慢性再発性多発性骨髄炎	Chronic recurrent multifocal osteomyelitis	H01117	http://www.geneontology.org/formats/oboInOwl#hasDbXref	慢性再発性多発性骨髄炎	Majeed syndrome	https://identifiers.org/kegg.disease:H01117
NANDO:1200869	http://nanbyodata.jp/ontology/NANDO_1200869	慢性再発性多発性骨髄炎	Chronic recurrent multifocal osteomyelitis	H01117	http://www.geneontology.org/formats/oboInOwl#hasDbXref	Majeed 症候群	Majeed syndrome	https://identifiers.org/kegg.disease:H01117
NANDO:1200870	http://nanbyodata.jp/ontology/NANDO_1200870	強直性脊椎炎	Ankylosing spondylitis	H01674	http://www.geneontology.org/formats/oboInOwl#hasDbXref	強直性脊椎炎	Ankylosing spondylitis	https://identifiers.org/kegg.disease:H01674
NANDO:1200870	http://nanbyodata.jp/ontology/NANDO_1200870	強直性脊椎炎	Ankylosing spondylitis	H01674	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ベヒテレフ病	Ankylosing spondylitis	https://identifiers.org/kegg.disease:H01674
NANDO:1200870	http://nanbyodata.jp/ontology/NANDO_1200870	強直性脊椎炎	Ankylosing spondylitis	H01674	http://www.geneontology.org/formats/oboInOwl#hasDbXref	強直性脊椎炎	Bechterew disease	https://identifiers.org/kegg.disease:H01674
NANDO:1200870	http://nanbyodata.jp/ontology/NANDO_1200870	強直性脊椎炎	Ankylosing spondylitis	H01674	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ベヒテレフ病	Bechterew disease	https://identifiers.org/kegg.disease:H01674
NANDO:1200871	http://nanbyodata.jp/ontology/NANDO_1200871	進行性骨化性線維異形成症	Fibrodysplasia ossificans progressiva	H00430	http://www.geneontology.org/formats/oboInOwl#hasDbXref	進行性骨化性線維異形成症	Fibrodysplasia ossificans progressiva	https://identifiers.org/kegg.disease:H00430
NANDO:1200871	http://nanbyodata.jp/ontology/NANDO_1200871	進行性骨化性線維異形成症	Fibrodysplasia ossificans progressiva	H00430	http://www.geneontology.org/formats/oboInOwl#hasDbXref	進行性骨化線維増殖症	Fibrodysplasia ossificans progressiva	https://identifiers.org/kegg.disease:H00430
NANDO:1200873	http://nanbyodata.jp/ontology/NANDO_1200873	骨形成不全症	Osteogenesis imperfecta	H00506	http://www.geneontology.org/formats/oboInOwl#hasDbXref	骨形成不全症	Osteogenesis imperfecta	https://identifiers.org/kegg.disease:H00506
NANDO:1200885	http://nanbyodata.jp/ontology/NANDO_1200885	先天性赤血球形成異常性貧血	Congenital dyserythropoietic anemia	H00917	http://www.geneontology.org/formats/oboInOwl#hasDbXref	先天性赤血球形成異常性貧血	Congenital dyserythropoietic anemia	https://identifiers.org/kegg.disease:H00917
NANDO:1200885	http://nanbyodata.jp/ontology/NANDO_1200885	先天性赤血球形成異常性貧血	Congenital dyserythropoietic anemia	H00917	http://www.geneontology.org/formats/oboInOwl#hasDbXref	先天性赤血球生成不全性貧血	Congenital dyserythropoietic anemia	https://identifiers.org/kegg.disease:H00917
NANDO:1200885	http://nanbyodata.jp/ontology/NANDO_1200885	先天性赤血球形成異常性貧血	Congenital dyserythropoietic anemia	H00917	http://www.geneontology.org/formats/oboInOwl#hasDbXref	先天性赤血球異形成貧血	Congenital dyserythropoietic anemia	https://identifiers.org/kegg.disease:H00917
NANDO:1200889	http://nanbyodata.jp/ontology/NANDO_1200889	後天性赤芽球癆	Acquired pure red cell aplasia	H01586	http://www.geneontology.org/formats/oboInOwl#hasDbXref	後天性赤芽球癆	Acquired pure red cell aplasia	https://identifiers.org/kegg.disease:H01586
NANDO:1200071	http://nanbyodata.jp/ontology/NANDO_1200071	Tay-Sachs病	Tay-Sachs disease	H02016	http://www.geneontology.org/formats/oboInOwl#hasDbXref	テイ・サックス病	Tay-Sachs disease	https://identifiers.org/kegg.disease:H02016
NANDO:1200071	http://nanbyodata.jp/ontology/NANDO_1200071	Tay-Sachs病	Tay-Sachs disease	H02016	http://www.geneontology.org/formats/oboInOwl#hasDbXref	GM2 ガングリオシドーシス I 型	Tay-Sachs disease	https://identifiers.org/kegg.disease:H02016
NANDO:1200071	http://nanbyodata.jp/ontology/NANDO_1200071	Tay-Sachs病	Tay-Sachs disease	H02016	http://www.geneontology.org/formats/oboInOwl#hasDbXref	テイ・サックス病	GM2 gangliosidoses type I	https://identifiers.org/kegg.disease:H02016
NANDO:1200071	http://nanbyodata.jp/ontology/NANDO_1200071	Tay-Sachs病	Tay-Sachs disease	H02016	http://www.geneontology.org/formats/oboInOwl#hasDbXref	GM2 ガングリオシドーシス I 型	GM2 gangliosidoses type I	https://identifiers.org/kegg.disease:H02016
NANDO:1200072	http://nanbyodata.jp/ontology/NANDO_1200072	サンドホフ病	Sandhoff disease	H02017	http://www.geneontology.org/formats/oboInOwl#hasDbXref	サンドホフ病	Sandhoff disease	https://identifiers.org/kegg.disease:H02017
NANDO:1200072	http://nanbyodata.jp/ontology/NANDO_1200072	サンドホフ病	Sandhoff disease	H02017	http://www.geneontology.org/formats/oboInOwl#hasDbXref	GM2 ガングリオシドーシス II 型	Sandhoff disease	https://identifiers.org/kegg.disease:H02017
NANDO:1200072	http://nanbyodata.jp/ontology/NANDO_1200072	サンドホフ病	Sandhoff disease	H02017	http://www.geneontology.org/formats/oboInOwl#hasDbXref	サンドホフ病	GM2 gangliosidoses type II	https://identifiers.org/kegg.disease:H02017
NANDO:1200072	http://nanbyodata.jp/ontology/NANDO_1200072	サンドホフ病	Sandhoff disease	H02017	http://www.geneontology.org/formats/oboInOwl#hasDbXref	GM2 ガングリオシドーシス II 型	GM2 gangliosidoses type II	https://identifiers.org/kegg.disease:H02017
NANDO:1200125	http://nanbyodata.jp/ontology/NANDO_1200125	ムコリピドーシスIII型	Mucolipidosis III	H02130	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ムコリピドーシス III 型	Mucolipidosis III	https://identifiers.org/kegg.disease:H02130
NANDO:1200125	http://nanbyodata.jp/ontology/NANDO_1200125	ムコリピドーシスIII型	Mucolipidosis III	H02130	http://www.geneontology.org/formats/oboInOwl#hasDbXref	偽 Hurler ポリジストロフィー	Mucolipidosis III	https://identifiers.org/kegg.disease:H02130
NANDO:1200125	http://nanbyodata.jp/ontology/NANDO_1200125	ムコリピドーシスIII型	Mucolipidosis III	H02130	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ムコリピドーシス III 型	Pseudo-Hurler polydystrophy	https://identifiers.org/kegg.disease:H02130
NANDO:1200125	http://nanbyodata.jp/ontology/NANDO_1200125	ムコリピドーシスIII型	Mucolipidosis III	H02130	http://www.geneontology.org/formats/oboInOwl#hasDbXref	偽 Hurler ポリジストロフィー	Pseudo-Hurler polydystrophy	https://identifiers.org/kegg.disease:H02130
NANDO:1200138	http://nanbyodata.jp/ontology/NANDO_1200138	ポンペ病	Pompe disease	H01940	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ポンペ病	Pompe disease	https://identifiers.org/kegg.disease:H01940
NANDO:1200138	http://nanbyodata.jp/ontology/NANDO_1200138	ポンペ病	Pompe disease	H01940	http://www.geneontology.org/formats/oboInOwl#hasDbXref	糖原病 II型	Pompe disease	https://identifiers.org/kegg.disease:H01940
NANDO:1200138	http://nanbyodata.jp/ontology/NANDO_1200138	ポンペ病	Pompe disease	H01940	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ポンペ病	Glycogen storage disease type II	https://identifiers.org/kegg.disease:H01940
NANDO:1200138	http://nanbyodata.jp/ontology/NANDO_1200138	ポンペ病	Pompe disease	H01940	http://www.geneontology.org/formats/oboInOwl#hasDbXref	糖原病 II型	Glycogen storage disease type II	https://identifiers.org/kegg.disease:H01940
NANDO:1200152	http://nanbyodata.jp/ontology/NANDO_1200152	乳児型神経セロイドリポフスチン症	Infantile neuronal ceroid lipofuscinosis	H02277	http://www.geneontology.org/formats/oboInOwl#hasDbXref	乳児型神経セロイドリポフスチン症	Infantile neuronal ceroid lipofuscinosis	https://identifiers.org/kegg.disease:H02277
NANDO:1200152	http://nanbyodata.jp/ontology/NANDO_1200152	乳児型神経セロイドリポフスチン症	Infantile neuronal ceroid lipofuscinosis	H02277	http://www.geneontology.org/formats/oboInOwl#hasDbXref	Santavuori-Haltia 病	Infantile neuronal ceroid lipofuscinosis	https://identifiers.org/kegg.disease:H02277
NANDO:1200152	http://nanbyodata.jp/ontology/NANDO_1200152	乳児型神経セロイドリポフスチン症	Infantile neuronal ceroid lipofuscinosis	H02277	http://www.geneontology.org/formats/oboInOwl#hasDbXref	乳児型神経セロイドリポフスチン症	Santavuori-Haltia disease	https://identifiers.org/kegg.disease:H02277
NANDO:1200152	http://nanbyodata.jp/ontology/NANDO_1200152	乳児型神経セロイドリポフスチン症	Infantile neuronal ceroid lipofuscinosis	H02277	http://www.geneontology.org/formats/oboInOwl#hasDbXref	Santavuori-Haltia 病	Santavuori-Haltia disease	https://identifiers.org/kegg.disease:H02277
NANDO:1200154	http://nanbyodata.jp/ontology/NANDO_1200154	若年型神経セロイドリポフスチン症	Juvenile neuronal ceroid lipofuscinosis	H02275	http://www.geneontology.org/formats/oboInOwl#hasDbXref	若年型神経セロイドリポフスチン症	Batten disease	https://identifiers.org/kegg.disease:H02275
NANDO:1200154	http://nanbyodata.jp/ontology/NANDO_1200154	若年型神経セロイドリポフスチン症	Juvenile neuronal ceroid lipofuscinosis	H02275	http://www.geneontology.org/formats/oboInOwl#hasDbXref	Spielmeyer-Vogt 病	Batten disease	https://identifiers.org/kegg.disease:H02275
NANDO:1200154	http://nanbyodata.jp/ontology/NANDO_1200154	若年型神経セロイドリポフスチン症	Juvenile neuronal ceroid lipofuscinosis	H02275	http://www.geneontology.org/formats/oboInOwl#hasDbXref	バッテン病	Batten disease	https://identifiers.org/kegg.disease:H02275
NANDO:1200154	http://nanbyodata.jp/ontology/NANDO_1200154	若年型神経セロイドリポフスチン症	Juvenile neuronal ceroid lipofuscinosis	H02275	http://www.geneontology.org/formats/oboInOwl#hasDbXref	若年型神経セロイドリポフスチン症	Juvenile neuronal ceroid lipofuscinoses	https://identifiers.org/kegg.disease:H02275
NANDO:1200154	http://nanbyodata.jp/ontology/NANDO_1200154	若年型神経セロイドリポフスチン症	Juvenile neuronal ceroid lipofuscinosis	H02275	http://www.geneontology.org/formats/oboInOwl#hasDbXref	Spielmeyer-Vogt 病	Juvenile neuronal ceroid lipofuscinoses	https://identifiers.org/kegg.disease:H02275
NANDO:1200154	http://nanbyodata.jp/ontology/NANDO_1200154	若年型神経セロイドリポフスチン症	Juvenile neuronal ceroid lipofuscinosis	H02275	http://www.geneontology.org/formats/oboInOwl#hasDbXref	バッテン病	Juvenile neuronal ceroid lipofuscinoses	https://identifiers.org/kegg.disease:H02275
NANDO:1200154	http://nanbyodata.jp/ontology/NANDO_1200154	若年型神経セロイドリポフスチン症	Juvenile neuronal ceroid lipofuscinosis	H02275	http://www.geneontology.org/formats/oboInOwl#hasDbXref	若年型神経セロイドリポフスチン症	Spielmeyer-Vogt disease	https://identifiers.org/kegg.disease:H02275
NANDO:1200154	http://nanbyodata.jp/ontology/NANDO_1200154	若年型神経セロイドリポフスチン症	Juvenile neuronal ceroid lipofuscinosis	H02275	http://www.geneontology.org/formats/oboInOwl#hasDbXref	Spielmeyer-Vogt 病	Spielmeyer-Vogt disease	https://identifiers.org/kegg.disease:H02275
NANDO:1200154	http://nanbyodata.jp/ontology/NANDO_1200154	若年型神経セロイドリポフスチン症	Juvenile neuronal ceroid lipofuscinosis	H02275	http://www.geneontology.org/formats/oboInOwl#hasDbXref	バッテン病	Spielmeyer-Vogt disease	https://identifiers.org/kegg.disease:H02275
NANDO:1200155	http://nanbyodata.jp/ontology/NANDO_1200155	成人型神経セロイドリポフスチン症	Adult neuronal ceroid lipofuscinosis	H02276	http://www.geneontology.org/formats/oboInOwl#hasDbXref	成人型神経セロイドリポフスチン症	Kufs disease	https://identifiers.org/kegg.disease:H02276
NANDO:1200155	http://nanbyodata.jp/ontology/NANDO_1200155	成人型神経セロイドリポフスチン症	Adult neuronal ceroid lipofuscinosis	H02276	http://www.geneontology.org/formats/oboInOwl#hasDbXref	Kufs 病	Kufs disease	https://identifiers.org/kegg.disease:H02276
NANDO:1200155	http://nanbyodata.jp/ontology/NANDO_1200155	成人型神経セロイドリポフスチン症	Adult neuronal ceroid lipofuscinosis	H02276	http://www.geneontology.org/formats/oboInOwl#hasDbXref	成人型神経セロイドリポフスチン症	Adult-onset neuronal ceroid lipofuscinosis	https://identifiers.org/kegg.disease:H02276
NANDO:1200155	http://nanbyodata.jp/ontology/NANDO_1200155	成人型神経セロイドリポフスチン症	Adult neuronal ceroid lipofuscinosis	H02276	http://www.geneontology.org/formats/oboInOwl#hasDbXref	Kufs 病	Adult-onset neuronal ceroid lipofuscinosis	https://identifiers.org/kegg.disease:H02276
NANDO:1200181	http://nanbyodata.jp/ontology/NANDO_1200181	複合体II欠損症	Mitochondrial complex II deficiency	H02005	http://www.geneontology.org/formats/oboInOwl#hasDbXref	コハク酸CoQ還元酵素欠損症	Mitochondrial complex II deficiency	https://identifiers.org/kegg.disease:H02005
NANDO:1200181	http://nanbyodata.jp/ontology/NANDO_1200181	複合体II欠損症	Mitochondrial complex II deficiency	H02005	http://www.geneontology.org/formats/oboInOwl#hasDbXref	コハク酸脱水素酵素欠損症	Mitochondrial complex II deficiency	https://identifiers.org/kegg.disease:H02005
NANDO:1200181	http://nanbyodata.jp/ontology/NANDO_1200181	複合体II欠損症	Mitochondrial complex II deficiency	H02005	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ミトコンドリア複合体 II 欠損症	Mitochondrial complex II deficiency	https://identifiers.org/kegg.disease:H02005
NANDO:1200181	http://nanbyodata.jp/ontology/NANDO_1200181	複合体II欠損症	Mitochondrial complex II deficiency	H02005	http://www.geneontology.org/formats/oboInOwl#hasDbXref	コハク酸CoQ還元酵素欠損症	Succinate CoQ reductase deficiency	https://identifiers.org/kegg.disease:H02005
NANDO:1200181	http://nanbyodata.jp/ontology/NANDO_1200181	複合体II欠損症	Mitochondrial complex II deficiency	H02005	http://www.geneontology.org/formats/oboInOwl#hasDbXref	コハク酸脱水素酵素欠損症	Succinate CoQ reductase deficiency	https://identifiers.org/kegg.disease:H02005
NANDO:1200181	http://nanbyodata.jp/ontology/NANDO_1200181	複合体II欠損症	Mitochondrial complex II deficiency	H02005	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ミトコンドリア複合体 II 欠損症	Succinate CoQ reductase deficiency	https://identifiers.org/kegg.disease:H02005
NANDO:1200181	http://nanbyodata.jp/ontology/NANDO_1200181	複合体II欠損症	Mitochondrial complex II deficiency	H02005	http://www.geneontology.org/formats/oboInOwl#hasDbXref	コハク酸CoQ還元酵素欠損症	Succinate dehydrogenase deficiency	https://identifiers.org/kegg.disease:H02005
NANDO:1200181	http://nanbyodata.jp/ontology/NANDO_1200181	複合体II欠損症	Mitochondrial complex II deficiency	H02005	http://www.geneontology.org/formats/oboInOwl#hasDbXref	コハク酸脱水素酵素欠損症	Succinate dehydrogenase deficiency	https://identifiers.org/kegg.disease:H02005
NANDO:1200181	http://nanbyodata.jp/ontology/NANDO_1200181	複合体II欠損症	Mitochondrial complex II deficiency	H02005	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ミトコンドリア複合体 II 欠損症	Succinate dehydrogenase deficiency	https://identifiers.org/kegg.disease:H02005
NANDO:1200215	http://nanbyodata.jp/ontology/NANDO_1200215	ウルリッヒ病	Ullrich disease	H01778	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ウルリッヒ型先天性筋ジストロフィー	Ullrich congenital muscular dystrophy	https://identifiers.org/kegg.disease:H01778
NANDO:1200215	http://nanbyodata.jp/ontology/NANDO_1200215	ウルリッヒ病	Ullrich disease	H01778	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ウルリッヒ病	Ullrich congenital muscular dystrophy	https://identifiers.org/kegg.disease:H01778
NANDO:1200215	http://nanbyodata.jp/ontology/NANDO_1200215	ウルリッヒ病	Ullrich disease	H01778	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ウルリッヒ型先天性筋ジストロフィー	Ullrich disease	https://identifiers.org/kegg.disease:H01778
NANDO:1200215	http://nanbyodata.jp/ontology/NANDO_1200215	ウルリッヒ病	Ullrich disease	H01778	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ウルリッヒ病	Ullrich disease	https://identifiers.org/kegg.disease:H01778
NANDO:1200217	http://nanbyodata.jp/ontology/NANDO_1200217	三好型ミオパチー	Miyoshi myopathy	H01965	http://www.geneontology.org/formats/oboInOwl#hasDbXref	三好型ミオパチー	Miyoshi myopathy	https://identifiers.org/kegg.disease:H01965
NANDO:1200217	http://nanbyodata.jp/ontology/NANDO_1200217	三好型ミオパチー	Miyoshi myopathy	H01965	http://www.geneontology.org/formats/oboInOwl#hasDbXref	三好型筋ジストロフィー	Miyoshi myopathy	https://identifiers.org/kegg.disease:H01965
NANDO:1200217	http://nanbyodata.jp/ontology/NANDO_1200217	三好型ミオパチー	Miyoshi myopathy	H01965	http://www.geneontology.org/formats/oboInOwl#hasDbXref	三好型ミオパチー	Miyoshi muscular dystrophy	https://identifiers.org/kegg.disease:H01965
NANDO:1200217	http://nanbyodata.jp/ontology/NANDO_1200217	三好型ミオパチー	Miyoshi myopathy	H01965	http://www.geneontology.org/formats/oboInOwl#hasDbXref	三好型筋ジストロフィー	Miyoshi muscular dystrophy	https://identifiers.org/kegg.disease:H01965
NANDO:1200218	http://nanbyodata.jp/ontology/NANDO_1200218	縁取り空胞を伴う遠位型ミオパチー	Distal myopathy with rimmed vacuoles	H02586	http://www.geneontology.org/formats/oboInOwl#hasDbXref	縁取り空胞を伴う遠位型ミオパチー	Distal myopathy with rimmed vacuoles	https://identifiers.org/kegg.disease:H02586
NANDO:1200219	http://nanbyodata.jp/ontology/NANDO_1200219	眼咽頭遠位型ミオパチー	Oculopharyngodistal myopathy	H02513	http://www.geneontology.org/formats/oboInOwl#hasDbXref	眼咽頭遠位型ミオパチー	Oculopharyngodistal myopathy	https://identifiers.org/kegg.disease:H02513
NANDO:1200221	http://nanbyodata.jp/ontology/NANDO_1200221	自己貪食空胞性ミオパチー	Autophagic vacuolar myopathy	H01781	http://www.geneontology.org/formats/oboInOwl#hasDbXref	自己貪食空胞性ミオパチー	Autophagic vacuolar myopathy	https://identifiers.org/kegg.disease:H01781
NANDO:1200224	http://nanbyodata.jp/ontology/NANDO_1200224	シュワルツ・ヤンペル症候群	Schwartz-Jampel syndrome	H01777	http://www.geneontology.org/formats/oboInOwl#hasDbXref	シュワルツ・ヤンペル症候群	Schwartz-Jampel syndrome	https://identifiers.org/kegg.disease:H01777
NANDO:1200234	http://nanbyodata.jp/ontology/NANDO_1200234	表皮水疱症	Epidermolysis bullosa	H01737	http://www.geneontology.org/formats/oboInOwl#hasDbXref	表皮水疱症	Epidermolysis bullosa	https://identifiers.org/kegg.disease:H01737
NANDO:1200278	http://nanbyodata.jp/ontology/NANDO_1200278	混合性結合組織病	Mixed connective tissue disease	H01710	http://www.geneontology.org/formats/oboInOwl#hasDbXref	混合性結合組織病	Mixed connective tissue disease	https://identifiers.org/kegg.disease:H01710
NANDO:1200283	http://nanbyodata.jp/ontology/NANDO_1200283	再発性多発軟骨炎	Relapsing polychondritis	H01758	http://www.geneontology.org/formats/oboInOwl#hasDbXref	再発性多発軟骨炎	Relapsing polychondritis	https://identifiers.org/kegg.disease:H01758
NANDO:1200323	http://nanbyodata.jp/ontology/NANDO_1200323	アデノシンデアミナーゼ欠損症	Adenosine deaminase deficiency	H02309	http://www.geneontology.org/formats/oboInOwl#hasDbXref	アデノシンデアミナーゼ欠損症	Adenosine deaminase deficiency	https://identifiers.org/kegg.disease:H02309
NANDO:1200324	http://nanbyodata.jp/ontology/NANDO_1200324	オーメン症候群	Omenn syndrome	H02554	http://www.geneontology.org/formats/oboInOwl#hasDbXref	Omenn 症候群	Omenn syndrome	https://identifiers.org/kegg.disease:H02554
NANDO:1200340	http://nanbyodata.jp/ontology/NANDO_1200340	高IgE症候群	Hyper-IgE syndrome	H01968	http://www.geneontology.org/formats/oboInOwl#hasDbXref	Buckley 症候群	Hyper-IgE syndrome	https://identifiers.org/kegg.disease:H01968
NANDO:1200340	http://nanbyodata.jp/ontology/NANDO_1200340	高IgE症候群	Hyper-IgE syndrome	H01968	http://www.geneontology.org/formats/oboInOwl#hasDbXref	Job 症候群	Hyper-IgE syndrome	https://identifiers.org/kegg.disease:H01968
NANDO:1200340	http://nanbyodata.jp/ontology/NANDO_1200340	高IgE症候群	Hyper-IgE syndrome	H01968	http://www.geneontology.org/formats/oboInOwl#hasDbXref	高 IgE 症候群	Hyper-IgE syndrome	https://identifiers.org/kegg.disease:H01968
NANDO:1200340	http://nanbyodata.jp/ontology/NANDO_1200340	高IgE症候群	Hyper-IgE syndrome	H01968	http://www.geneontology.org/formats/oboInOwl#hasDbXref	Buckley 症候群	Buckley syndrome	https://identifiers.org/kegg.disease:H01968
NANDO:1200340	http://nanbyodata.jp/ontology/NANDO_1200340	高IgE症候群	Hyper-IgE syndrome	H01968	http://www.geneontology.org/formats/oboInOwl#hasDbXref	Job 症候群	Buckley syndrome	https://identifiers.org/kegg.disease:H01968
NANDO:1200340	http://nanbyodata.jp/ontology/NANDO_1200340	高IgE症候群	Hyper-IgE syndrome	H01968	http://www.geneontology.org/formats/oboInOwl#hasDbXref	高 IgE 症候群	Buckley syndrome	https://identifiers.org/kegg.disease:H01968
NANDO:1200340	http://nanbyodata.jp/ontology/NANDO_1200340	高IgE症候群	Hyper-IgE syndrome	H01968	http://www.geneontology.org/formats/oboInOwl#hasDbXref	Buckley 症候群	Job syndrome	https://identifiers.org/kegg.disease:H01968
NANDO:1200340	http://nanbyodata.jp/ontology/NANDO_1200340	高IgE症候群	Hyper-IgE syndrome	H01968	http://www.geneontology.org/formats/oboInOwl#hasDbXref	Job 症候群	Job syndrome	https://identifiers.org/kegg.disease:H01968
NANDO:1200340	http://nanbyodata.jp/ontology/NANDO_1200340	高IgE症候群	Hyper-IgE syndrome	H01968	http://www.geneontology.org/formats/oboInOwl#hasDbXref	高 IgE 症候群	Job syndrome	https://identifiers.org/kegg.disease:H01968
NANDO:1200350	http://nanbyodata.jp/ontology/NANDO_1200350	チェディアック・東症候群	Chédiak-Higashi syndrome	H02021	http://www.geneontology.org/formats/oboInOwl#hasDbXref	チェディアック・東症候群	Chediak-Higashi syndrome	https://identifiers.org/kegg.disease:H02021
NANDO:1200351	http://nanbyodata.jp/ontology/NANDO_1200351	X連鎖リンパ増殖症候群	X-linked lymphoproliferative syndrome	H01969	http://www.geneontology.org/formats/oboInOwl#hasDbXref	Duncan 病	X-linked lymphoproliferative syndrome	https://identifiers.org/kegg.disease:H01969
NANDO:1200351	http://nanbyodata.jp/ontology/NANDO_1200351	X連鎖リンパ増殖症候群	X-linked lymphoproliferative syndrome	H01969	http://www.geneontology.org/formats/oboInOwl#hasDbXref	X連鎖性リンパ球増殖症候群	X-linked lymphoproliferative syndrome	https://identifiers.org/kegg.disease:H01969
NANDO:1200351	http://nanbyodata.jp/ontology/NANDO_1200351	X連鎖リンパ増殖症候群	X-linked lymphoproliferative syndrome	H01969	http://www.geneontology.org/formats/oboInOwl#hasDbXref	Duncan 病	Duncan disease	https://identifiers.org/kegg.disease:H01969
NANDO:1200351	http://nanbyodata.jp/ontology/NANDO_1200351	X連鎖リンパ増殖症候群	X-linked lymphoproliferative syndrome	H01969	http://www.geneontology.org/formats/oboInOwl#hasDbXref	X連鎖性リンパ球増殖症候群	Duncan disease	https://identifiers.org/kegg.disease:H01969
NANDO:1200358	http://nanbyodata.jp/ontology/NANDO_1200358	ミエロペルオキシダーゼ欠損症	Myeloperoxidase deficiency	H02025	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ミエロペルオキシダーゼ欠損症	Myeloperoxidase deficiency	https://identifiers.org/kegg.disease:H02025
NANDO:1200381	http://nanbyodata.jp/ontology/NANDO_1200381	中枢性思春期早発症	Central precocious puberty	H02018	http://www.geneontology.org/formats/oboInOwl#hasDbXref	中枢性思春期早発症	Central precocious puberty	https://identifiers.org/kegg.disease:H02018
NANDO:1200386	http://nanbyodata.jp/ontology/NANDO_1200386	下垂体性成長ホルモン分泌亢進症	Diencephalo-hypophysial dysfunction-syndrome of abnormal secretion of growth hormone	H01864	http://www.geneontology.org/formats/oboInOwl#hasDbXref	下垂体性成長ホルモン分泌亢進症	Excessive secretion of growth hormone	https://identifiers.org/kegg.disease:H01864
NANDO:1200387	http://nanbyodata.jp/ontology/NANDO_1200387	下垂体前葉機能低下症	Hypopituitarism syndrome	H01700	http://www.geneontology.org/formats/oboInOwl#hasDbXref	下垂体前葉機能低下症	Hypopituitarism	https://identifiers.org/kegg.disease:H01700
NANDO:1200403	http://nanbyodata.jp/ontology/NANDO_1200403	先天性副腎低形成症	Congenital adrenal hypoplasia	H01772	http://www.geneontology.org/formats/oboInOwl#hasDbXref	先天性副腎低形成症	Adrenal hypoplasia, congenital	https://identifiers.org/kegg.disease:H01772
NANDO:1200403	http://nanbyodata.jp/ontology/NANDO_1200403	先天性副腎低形成症	Congenital adrenal hypoplasia	H01772	http://www.geneontology.org/formats/oboInOwl#hasDbXref	X連鎖性アジソン病	Adrenal hypoplasia, congenital	https://identifiers.org/kegg.disease:H01772
NANDO:1200403	http://nanbyodata.jp/ontology/NANDO_1200403	先天性副腎低形成症	Congenital adrenal hypoplasia	H01772	http://www.geneontology.org/formats/oboInOwl#hasDbXref	先天性副腎低形成症	X-linked addison disease	https://identifiers.org/kegg.disease:H01772
NANDO:1200403	http://nanbyodata.jp/ontology/NANDO_1200403	先天性副腎低形成症	Congenital adrenal hypoplasia	H01772	http://www.geneontology.org/formats/oboInOwl#hasDbXref	X連鎖性アジソン病	X-linked addison disease	https://identifiers.org/kegg.disease:H01772
NANDO:1200406	http://nanbyodata.jp/ontology/NANDO_1200406	IMAge症候群	IMAge syndrome	H02319	http://www.geneontology.org/formats/oboInOwl#hasDbXref	IMAGE 症候群	IMAGE syndrome	https://identifiers.org/kegg.disease:H02319
NANDO:1200416	http://nanbyodata.jp/ontology/NANDO_1200416	特発性間質性肺炎	Idiopathic interstitial pneumonia	H01716	http://www.geneontology.org/formats/oboInOwl#hasDbXref	特発性間質性肺炎	Idiopathic interstitial pneumonias	https://identifiers.org/kegg.disease:H01716
NANDO:1200426	http://nanbyodata.jp/ontology/NANDO_1200426	肺静脈閉塞症／肺毛細血管腫症	Pulmonary veno-occlusive disease / pulmonary capillary hemangiomatosis	H01866	http://www.geneontology.org/formats/oboInOwl#hasDbXref	肺静脈閉塞症／肺毛細血管腫症	Pulmonary veno-occlusive disease and pulmonary capillary hemangiomatosis	https://identifiers.org/kegg.disease:H01866
NANDO:1200454	http://nanbyodata.jp/ontology/NANDO_1200454	好酸球性消化管疾患	Eosinophilic gastrointestinal disorders	H01782	http://www.geneontology.org/formats/oboInOwl#hasDbXref	好酸球性消化管疾患	Eosinophilic gastrointestinal disorder	https://identifiers.org/kegg.disease:H01782
NANDO:1200459	http://nanbyodata.jp/ontology/NANDO_1200459	巨大膀胱短小結腸腸管蠕動不全症	Megacystis-microcolon-intestinal hypoperistalsis syndrome	H01869	http://www.geneontology.org/formats/oboInOwl#hasDbXref	巨大膀胱短小結腸腸管蠕動不全症	Megacystis microcolon intestinal hypoperistalsis syndrome	https://identifiers.org/kegg.disease:H01869
NANDO:1200460	http://nanbyodata.jp/ontology/NANDO_1200460	腸管神経節細胞僅少症	Congenital isolated hypoganglionosis	H01871	http://www.geneontology.org/formats/oboInOwl#hasDbXref	腸管神経節細胞僅少症	Isolated hypoganglionosis	https://identifiers.org/kegg.disease:H01871
NANDO:1200463	http://nanbyodata.jp/ontology/NANDO_1200463	コステロ症候群	Costello syndrome	H01747	http://www.geneontology.org/formats/oboInOwl#hasDbXref	コステロ症候群	Costello syndrome	https://identifiers.org/kegg.disease:H01747
NANDO:1200467	http://nanbyodata.jp/ontology/NANDO_1200467	マックル・ウェルズ症候群	Muckle-Wells syndrome	H02555	http://www.geneontology.org/formats/oboInOwl#hasDbXref	マックル-ウェルズ症候群	Muckle-Wells syndrome	https://identifiers.org/kegg.disease:H02555
NANDO:1200477	http://nanbyodata.jp/ontology/NANDO_1200477	先天性ミオパチー	Congenital myopathy	H01810	http://www.geneontology.org/formats/oboInOwl#hasDbXref	先天性ミオパチー	Congenital myopathy	https://identifiers.org/kegg.disease:H01810
NANDO:1200488	http://nanbyodata.jp/ontology/NANDO_1200488	デュシェンヌ型筋ジストロフィー	Duchenne muscular dystrophy	H01963	http://www.geneontology.org/formats/oboInOwl#hasDbXref	デュシェンヌ型筋ジストロフィー	Duchenne muscular dystrophy	https://identifiers.org/kegg.disease:H01963
NANDO:1200489	http://nanbyodata.jp/ontology/NANDO_1200489	ベッカー型筋ジストロフィー	Becker muscular dystrophy	H01964	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ベッカー型筋ジストロフィー	Becker muscular dystrophy	https://identifiers.org/kegg.disease:H01964
NANDO:1200494	http://nanbyodata.jp/ontology/NANDO_1200494	福山型先天性筋ジストロフィー	Fukuyama type congenital muscular dystrophy	H01957	http://www.geneontology.org/formats/oboInOwl#hasDbXref	福山型先天性筋ジストロフィー	Fukuyama congenital muscular dystrophy	https://identifiers.org/kegg.disease:H01957
NANDO:1200496	http://nanbyodata.jp/ontology/NANDO_1200496	非ジストロフィー性ミオトニー症候群	Non-dystrophic myotonia	H01780	http://www.geneontology.org/formats/oboInOwl#hasDbXref	非ジストロフィー性ミオトニー症候群	Non-dystrophic myotonia	https://identifiers.org/kegg.disease:H01780
NANDO:1200505	http://nanbyodata.jp/ontology/NANDO_1200505	アトピー性脊髄炎	Atopic myelitis	H01863	http://www.geneontology.org/formats/oboInOwl#hasDbXref	アトピー性脊髄炎	Atopic myelitis	https://identifiers.org/kegg.disease:H01863
NANDO:1200505	http://nanbyodata.jp/ontology/NANDO_1200505	アトピー性脊髄炎	Atopic myelitis	H01863	http://www.geneontology.org/formats/oboInOwl#hasDbXref	アトピー性脊髄炎	Eosinophilic myelitis	https://identifiers.org/kegg.disease:H01863
NANDO:1200510	http://nanbyodata.jp/ontology/NANDO_1200510	アイザックス症候群	Isaacs syndrome	H01804	http://www.geneontology.org/formats/oboInOwl#hasDbXref	アイザックス症候群	Isaacs syndrome	https://identifiers.org/kegg.disease:H01804
NANDO:1200543	http://nanbyodata.jp/ontology/NANDO_1200543	脳表ヘモジデリン沈着症	Superficial siderosis	H01846	http://www.geneontology.org/formats/oboInOwl#hasDbXref	脳表ヘモジデリン沈着症	Superficial siderosis	https://identifiers.org/kegg.disease:H01846
NANDO:1200546	http://nanbyodata.jp/ontology/NANDO_1200546	神経軸索スフェロイド形成を伴う遺伝性びまん性白質脳症	Hereditary diffuse leukoencephalopathy with spheroid	H01807	http://www.geneontology.org/formats/oboInOwl#hasDbXref	神経軸索スフェロイド形成を伴う遺伝性びまん性白質脳症	Hereditary diffuse leukoencephalopathy with spheroids	https://identifiers.org/kegg.disease:H01807
NANDO:1200551	http://nanbyodata.jp/ontology/NANDO_1200551	ビッカースタッフ脳幹脳炎	Bickerstaff's brainstem encephalitis	H01842	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ビッカースタッフ脳幹脳炎	Bickerstaff brainstem encephalitis	https://identifiers.org/kegg.disease:H01842
NANDO:1200552	http://nanbyodata.jp/ontology/NANDO_1200552	痙攣重積型（二相性）急性脳症	Acute encephalopathy with biphasic seizures and late reduced diffusion	H01841	http://www.geneontology.org/formats/oboInOwl#hasDbXref	痙攣重積型 (二相性) 急性脳症	Acute encephalopathy with biphasic seizures and late reduced diffusion	https://identifiers.org/kegg.disease:H01841
NANDO:1200553	http://nanbyodata.jp/ontology/NANDO_1200553	先天性無痛無汗症	Congenital insensitivity to pain with anhidrosis	H01836	http://www.geneontology.org/formats/oboInOwl#hasDbXref	先天性無痛無汗症	Congenital pain insensitivity with anhidrosis	https://identifiers.org/kegg.disease:H01836
NANDO:1200558	http://nanbyodata.jp/ontology/NANDO_1200558	先天性核上性球麻痺	Congenital suprabulbar paresis	H01837	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ウースター・ドロート症候群	Congenital suprabulbar paresis	https://identifiers.org/kegg.disease:H01837
NANDO:1200558	http://nanbyodata.jp/ontology/NANDO_1200558	先天性核上性球麻痺	Congenital suprabulbar paresis	H01837	http://www.geneontology.org/formats/oboInOwl#hasDbXref	先天性核上性球麻痺	Congenital suprabulbar paresis	https://identifiers.org/kegg.disease:H01837
NANDO:1200558	http://nanbyodata.jp/ontology/NANDO_1200558	先天性核上性球麻痺	Congenital suprabulbar paresis	H01837	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ウースター・ドロート症候群	Worster Drought syndrome	https://identifiers.org/kegg.disease:H01837
NANDO:1200558	http://nanbyodata.jp/ontology/NANDO_1200558	先天性核上性球麻痺	Congenital suprabulbar paresis	H01837	http://www.geneontology.org/formats/oboInOwl#hasDbXref	先天性核上性球麻痺	Worster Drought syndrome	https://identifiers.org/kegg.disease:H01837
NANDO:1200559	http://nanbyodata.jp/ontology/NANDO_1200559	メビウス症候群	Moebius syndrome	H01840	http://www.geneontology.org/formats/oboInOwl#hasDbXref	メビウス症候群	Moebius syndrome	https://identifiers.org/kegg.disease:H01840
NANDO:1200559	http://nanbyodata.jp/ontology/NANDO_1200559	メビウス症候群	Moebius syndrome	H01840	http://www.geneontology.org/formats/oboInOwl#hasDbXref	メビウス症候群	Mobius syndrome	https://identifiers.org/kegg.disease:H01840
NANDO:1200562	http://nanbyodata.jp/ontology/NANDO_1200562	アイカルディ症候群	Aicardi syndrome	H01776	http://www.geneontology.org/formats/oboInOwl#hasDbXref	アイカルディ症候群	Aicardi syndrome	https://identifiers.org/kegg.disease:H01776
NANDO:1200563	http://nanbyodata.jp/ontology/NANDO_1200563	片側巨脳症	Hemimegalencephaly	H01833	http://www.geneontology.org/formats/oboInOwl#hasDbXref	片側巨脳症	Hemimegalencephaly	https://identifiers.org/kegg.disease:H01833
NANDO:1200574	http://nanbyodata.jp/ontology/NANDO_1200574	神経細胞移動異常症	Neuronal migration defects	H01835	http://www.geneontology.org/formats/oboInOwl#hasDbXref	神経細胞移動異常症	Neuronal migration disorder	https://identifiers.org/kegg.disease:H01835
NANDO:1200587	http://nanbyodata.jp/ontology/NANDO_1200587	ドラベ症候群	Dravet syndrome	H01818	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ドラベ症候群	Dravet syndrome	https://identifiers.org/kegg.disease:H01818
NANDO:1200588	http://nanbyodata.jp/ontology/NANDO_1200588	海馬硬化を伴う内側側頭葉てんかん	Mesial temporal lobe epilepsy with bilateral hippocampal sclerosis	H01826	http://www.geneontology.org/formats/oboInOwl#hasDbXref	海馬硬化を伴う内側側頭葉てんかん	Mesial temporal lobe epilepsy with hippocampal sclerosis	https://identifiers.org/kegg.disease:H01826
NANDO:1200589	http://nanbyodata.jp/ontology/NANDO_1200589	ミオクロニー欠神てんかん	Myoclonic absence epilepsy	H01822	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ミオクロニー欠神てんかん	Epilepsy with myoclonic absence	https://identifiers.org/kegg.disease:H01822
NANDO:1200590	http://nanbyodata.jp/ontology/NANDO_1200590	ミオクロニー脱力発作を伴うてんかん	Epilepsy with myoclonic atonic seizures	H01823	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ミオクロニー脱力発作を伴うてんかん	Doose syndrome	https://identifiers.org/kegg.disease:H01823
NANDO:1200590	http://nanbyodata.jp/ontology/NANDO_1200590	ミオクロニー脱力発作を伴うてんかん	Epilepsy with myoclonic atonic seizures	H01823	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ドーゼ症候群	Doose syndrome	https://identifiers.org/kegg.disease:H01823
NANDO:1200590	http://nanbyodata.jp/ontology/NANDO_1200590	ミオクロニー脱力発作を伴うてんかん	Epilepsy with myoclonic atonic seizures	H01823	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ミオクロニー脱力発作を伴うてんかん	Myoclonic-astatic epilepsy	https://identifiers.org/kegg.disease:H01823
NANDO:1200590	http://nanbyodata.jp/ontology/NANDO_1200590	ミオクロニー脱力発作を伴うてんかん	Epilepsy with myoclonic atonic seizures	H01823	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ドーゼ症候群	Myoclonic-astatic epilepsy	https://identifiers.org/kegg.disease:H01823
NANDO:1200591	http://nanbyodata.jp/ontology/NANDO_1200591	レノックス・ガストー症候群	Lennox-Gastaut syndrome	H01813	http://www.geneontology.org/formats/oboInOwl#hasDbXref	レノックス・ガストー症候群	Lennox-Gastaut syndrome	https://identifiers.org/kegg.disease:H01813
NANDO:1200594	http://nanbyodata.jp/ontology/NANDO_1200594	早期ミオクロニー脳症	Early myoclonic encephalopathy	H01819	http://www.geneontology.org/formats/oboInOwl#hasDbXref	早期ミオクロニー脳症	Early myoclonic encephalopathy	https://identifiers.org/kegg.disease:H01819
NANDO:1200595	http://nanbyodata.jp/ontology/NANDO_1200595	遊走性焦点発作を伴う乳児てんかん	Epilepsy of infancy with migrating focal seizures	H01815	http://www.geneontology.org/formats/oboInOwl#hasDbXref	遊走性焦点発作を伴う乳児てんかん	Malignant migrating partial seizures in infancy	https://identifiers.org/kegg.disease:H01815
NANDO:1200596	http://nanbyodata.jp/ontology/NANDO_1200596	片側痙攣・片麻痺・てんかん症候群	Hemiconvulsion-hemiplegia-epilepsy syndrome	H01808	http://www.geneontology.org/formats/oboInOwl#hasDbXref	片側痙攣・片麻痺・てんかん症候群	Hemiconvulsion-hemiplegia-epilepsy syndrome	https://identifiers.org/kegg.disease:H01808
NANDO:1200597	http://nanbyodata.jp/ontology/NANDO_1200597	環状20番染色体症候群	Ring chromosome 20 syndrome	H01831	http://www.geneontology.org/formats/oboInOwl#hasDbXref	環状２０番染色体症候群	Ring chromosome 20 syndrome	https://identifiers.org/kegg.disease:H01831
NANDO:1200598	http://nanbyodata.jp/ontology/NANDO_1200598	ラスムッセン脳炎	Rasmussen's encephalitis	H01812	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ラスムッセン脳炎	Rasmussen encephalitis	https://identifiers.org/kegg.disease:H01812
NANDO:1200598	http://nanbyodata.jp/ontology/NANDO_1200598	ラスムッセン脳炎	Rasmussen's encephalitis	H01812	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ラスムッセン症候群	Rasmussen encephalitis	https://identifiers.org/kegg.disease:H01812
NANDO:1200598	http://nanbyodata.jp/ontology/NANDO_1200598	ラスムッセン脳炎	Rasmussen's encephalitis	H01812	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ラスムッセン脳炎	Rasmussen syndrome	https://identifiers.org/kegg.disease:H01812
NANDO:1200598	http://nanbyodata.jp/ontology/NANDO_1200598	ラスムッセン脳炎	Rasmussen's encephalitis	H01812	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ラスムッセン症候群	Rasmussen syndrome	https://identifiers.org/kegg.disease:H01812
NANDO:1200600	http://nanbyodata.jp/ontology/NANDO_1200600	難治頻回部分発作重積型急性脳炎	Acute encephalitis with refractory, repetitive partial seizures	H01829	http://www.geneontology.org/formats/oboInOwl#hasDbXref	難治頻回部分発作重積型急性脳炎	Acute encephalitis with refractory repetitive partial seizures	https://identifiers.org/kegg.disease:H01829
NANDO:1200606	http://nanbyodata.jp/ontology/NANDO_1200606	スタージ・ウェーバー症候群	Sturge-Weber syndrome	H01809	http://www.geneontology.org/formats/oboInOwl#hasDbXref	スタージ・ウェーバー症候群	Sturge-Weber syndrome	https://identifiers.org/kegg.disease:H01809
NANDO:1200609	http://nanbyodata.jp/ontology/NANDO_1200609	先天性魚鱗癬	Congenital ichthyosis	H01771	http://www.geneontology.org/formats/oboInOwl#hasDbXref	先天性魚鱗癬	Congenital ichthyosis	https://identifiers.org/kegg.disease:H01771
NANDO:1200636	http://nanbyodata.jp/ontology/NANDO_1200636	特発性後天性全身性無汗症	Acquired idiopathic generalized anhidrosis	H01848	http://www.geneontology.org/formats/oboInOwl#hasDbXref	特発性後天性全身性無汗症	Acquired idiopathic generalized anhidrosis	https://identifiers.org/kegg.disease:H01848
NANDO:1200640	http://nanbyodata.jp/ontology/NANDO_1200640	グリセリ症候群	Griscelli syndrome	H02022	http://www.geneontology.org/formats/oboInOwl#hasDbXref	グリセリ症候群	Griscelli syndrome	https://identifiers.org/kegg.disease:H02022
NANDO:1200654	http://nanbyodata.jp/ontology/NANDO_1200654	オクシピタル・ホーン症候群	Occipital horn syndrome	H01859	http://www.geneontology.org/formats/oboInOwl#hasDbXref	オクシピタル・ホーン症候群	Occipital horn syndrome	https://identifiers.org/kegg.disease:H01859
NANDO:1200659	http://nanbyodata.jp/ontology/NANDO_1200659	ウィーバー症候群	Weaver syndrome	H01751	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ウィーバー症候群	Weaver syndrome	https://identifiers.org/kegg.disease:H01751
NANDO:1200662	http://nanbyodata.jp/ontology/NANDO_1200662	有馬症候群	Arima syndrome	H01811	http://www.geneontology.org/formats/oboInOwl#hasDbXref	有馬症候群	Arima syndrome	https://identifiers.org/kegg.disease:H01811
NANDO:1200665	http://nanbyodata.jp/ontology/NANDO_1200665	ATR-X症候群	ATR-X syndrome	H01752	http://www.geneontology.org/formats/oboInOwl#hasDbXref	X連鎖アルファサラセミア精神遅滞症候群	ATR-X syndrome	https://identifiers.org/kegg.disease:H01752
NANDO:1200665	http://nanbyodata.jp/ontology/NANDO_1200665	ATR-X症候群	ATR-X syndrome	H01752	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ATR-X 症候群	ATR-X syndrome	https://identifiers.org/kegg.disease:H01752
NANDO:1200665	http://nanbyodata.jp/ontology/NANDO_1200665	ATR-X症候群	ATR-X syndrome	H01752	http://www.geneontology.org/formats/oboInOwl#hasDbXref	X連鎖アルファサラセミア精神遅滞症候群	X-linked alpha-thalassemia/mental retardation syndrome	https://identifiers.org/kegg.disease:H01752
NANDO:1200665	http://nanbyodata.jp/ontology/NANDO_1200665	ATR-X症候群	ATR-X syndrome	H01752	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ATR-X 症候群	X-linked alpha-thalassemia/mental retardation syndrome	https://identifiers.org/kegg.disease:H01752
NANDO:1200666	http://nanbyodata.jp/ontology/NANDO_1200666	クルーゾン症候群	Crouzon's syndrome	H01754	http://www.geneontology.org/formats/oboInOwl#hasDbXref	クルーゾン症候群	Crouzon syndrome	https://identifiers.org/kegg.disease:H01754
NANDO:1200667	http://nanbyodata.jp/ontology/NANDO_1200667	アペール症候群	Apert syndrome	H01755	http://www.geneontology.org/formats/oboInOwl#hasDbXref	アペール症候群	Apert syndrome	https://identifiers.org/kegg.disease:H01755
NANDO:1200668	http://nanbyodata.jp/ontology/NANDO_1200668	ファイファー症候群	Pfeiffer syndrome	H01756	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ファイファー症候群	Pfeiffer syndrome	https://identifiers.org/kegg.disease:H01756
NANDO:1200669	http://nanbyodata.jp/ontology/NANDO_1200669	アントレー・ビクスラー症候群	Antley-Bixler syndrome	H01753	http://www.geneontology.org/formats/oboInOwl#hasDbXref	アントレー・ビクスラー症候群	Antley-Bixler syndrome	https://identifiers.org/kegg.disease:H01753
NANDO:1200671	http://nanbyodata.jp/ontology/NANDO_1200671	ロスムンド・トムソン症候群	Rothmund-Thomson syndrome	H01734	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ロスムンド・トムソン症候群	Rothmund-Thomson syndrome	https://identifiers.org/kegg.disease:H01734
NANDO:1200673	http://nanbyodata.jp/ontology/NANDO_1200673	多脾症候群	Polysplenia syndrome	H01764	http://www.geneontology.org/formats/oboInOwl#hasDbXref	多脾症候群	Polysplenia syndrome	https://identifiers.org/kegg.disease:H01764
NANDO:1200676	http://nanbyodata.jp/ontology/NANDO_1200676	ウェルナー症候群	Werner syndrome	H01733	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ウェルナー症候群	Werner syndrome	https://identifiers.org/kegg.disease:H01733
NANDO:1200680	http://nanbyodata.jp/ontology/NANDO_1200680	ヌーナン症候群	Noonan syndrome	H01738	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ヌーナン症候群	Noonan syndrome	https://identifiers.org/kegg.disease:H01738
NANDO:1200681	http://nanbyodata.jp/ontology/NANDO_1200681	ヤング・シンプソン症候群	Young-Simpson syndrome	H01793	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ヤング・シンプソン症候群	Young-Simpson syndrome	https://identifiers.org/kegg.disease:H01793
NANDO:1200681	http://nanbyodata.jp/ontology/NANDO_1200681	ヤング・シンプソン症候群	Young-Simpson syndrome	H01793	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ヤング・シンプソン症候群	Say-Barber-Biesecker-Young-Simpson syndrome	https://identifiers.org/kegg.disease:H01793
NANDO:1200681	http://nanbyodata.jp/ontology/NANDO_1200681	ヤング・シンプソン症候群	Young-Simpson syndrome	H01793	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ヤング・シンプソン症候群	Say-Barber-Biesecker variant of Ohdo syndrome	https://identifiers.org/kegg.disease:H01793
NANDO:1200682	http://nanbyodata.jp/ontology/NANDO_1200682	1ｐ36欠失症候群	1p36 deletion syndrome	H01792	http://www.geneontology.org/formats/oboInOwl#hasDbXref	1p36 欠失症候群	1p36 deletion syndrome	https://identifiers.org/kegg.disease:H01792
NANDO:1200683	http://nanbyodata.jp/ontology/NANDO_1200683	4p欠失症候群	4p deletion syndrome	H01773	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ウォルフ・ヒルシュホーン症候群	4p deletion syndrome	https://identifiers.org/kegg.disease:H01773
NANDO:1200683	http://nanbyodata.jp/ontology/NANDO_1200683	4p欠失症候群	4p deletion syndrome	H01773	http://www.geneontology.org/formats/oboInOwl#hasDbXref	4p 欠失症候群	4p deletion syndrome	https://identifiers.org/kegg.disease:H01773
NANDO:1200683	http://nanbyodata.jp/ontology/NANDO_1200683	4p欠失症候群	4p deletion syndrome	H01773	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ウォルフ・ヒルシュホーン症候群	Wolf-Hirschhorn syndrome	https://identifiers.org/kegg.disease:H01773
NANDO:1200683	http://nanbyodata.jp/ontology/NANDO_1200683	4p欠失症候群	4p deletion syndrome	H01773	http://www.geneontology.org/formats/oboInOwl#hasDbXref	4p 欠失症候群	Wolf-Hirschhorn syndrome	https://identifiers.org/kegg.disease:H01773
NANDO:1200685	http://nanbyodata.jp/ontology/NANDO_1200685	第14番染色体父親性ダイソミー症候群	Paternal uniparental disomy of chromosome 14	H01801	http://www.geneontology.org/formats/oboInOwl#hasDbXref	鏡・緒方症候群	Kagami-Ogata syndrome	https://identifiers.org/kegg.disease:H01801
NANDO:1200685	http://nanbyodata.jp/ontology/NANDO_1200685	第14番染色体父親性ダイソミー症候群	Paternal uniparental disomy of chromosome 14	H01801	http://www.geneontology.org/formats/oboInOwl#hasDbXref	第１４番染色体父親性ダイソミー症候群	Kagami-Ogata syndrome	https://identifiers.org/kegg.disease:H01801
NANDO:1200685	http://nanbyodata.jp/ontology/NANDO_1200685	第14番染色体父親性ダイソミー症候群	Paternal uniparental disomy of chromosome 14	H01801	http://www.geneontology.org/formats/oboInOwl#hasDbXref	鏡・緒方症候群	Paternal uniparental disomy 14	https://identifiers.org/kegg.disease:H01801
NANDO:1200685	http://nanbyodata.jp/ontology/NANDO_1200685	第14番染色体父親性ダイソミー症候群	Paternal uniparental disomy of chromosome 14	H01801	http://www.geneontology.org/formats/oboInOwl#hasDbXref	第１４番染色体父親性ダイソミー症候群	Paternal uniparental disomy 14	https://identifiers.org/kegg.disease:H01801
NANDO:1200686	http://nanbyodata.jp/ontology/NANDO_1200686	アンジェルマン症候群	Angelman syndrome	H01732	http://www.geneontology.org/formats/oboInOwl#hasDbXref	アンジェルマン症候群	Angelman syndrome	https://identifiers.org/kegg.disease:H01732
NANDO:1200687	http://nanbyodata.jp/ontology/NANDO_1200687	スミス・マギニス症候群	Smith-Magenis syndrome	H01791	http://www.geneontology.org/formats/oboInOwl#hasDbXref	スミス・マギニス症候群	Smith-Magenis syndrome	https://identifiers.org/kegg.disease:H01791
NANDO:1200689	http://nanbyodata.jp/ontology/NANDO_1200689	エマヌエル症候群	Emanuel syndrome	H01790	http://www.geneontology.org/formats/oboInOwl#hasDbXref	エマヌエル症候群	Emanuel syndrome	https://identifiers.org/kegg.disease:H01790
NANDO:1200689	http://nanbyodata.jp/ontology/NANDO_1200689	エマヌエル症候群	Emanuel syndrome	H01790	http://www.geneontology.org/formats/oboInOwl#hasDbXref	22番過剰派生染色体症候群	Emanuel syndrome	https://identifiers.org/kegg.disease:H01790
NANDO:1200689	http://nanbyodata.jp/ontology/NANDO_1200689	エマヌエル症候群	Emanuel syndrome	H01790	http://www.geneontology.org/formats/oboInOwl#hasDbXref	エマヌエル症候群	Supernumerary derivative 22 syndrome	https://identifiers.org/kegg.disease:H01790
NANDO:1200689	http://nanbyodata.jp/ontology/NANDO_1200689	エマヌエル症候群	Emanuel syndrome	H01790	http://www.geneontology.org/formats/oboInOwl#hasDbXref	22番過剰派生染色体症候群	Supernumerary derivative 22 syndrome	https://identifiers.org/kegg.disease:H01790
NANDO:1200690	http://nanbyodata.jp/ontology/NANDO_1200690	脆弱Ｘ症候群関連疾患	Fragile X syndrome related diseases	H01731	http://www.geneontology.org/formats/oboInOwl#hasDbXref	脆弱Ｘ症候群関連疾患	Fragile X tremor/ataxia syndrome	https://identifiers.org/kegg.disease:H01731
NANDO:1200690	http://nanbyodata.jp/ontology/NANDO_1200690	脆弱Ｘ症候群関連疾患	Fragile X syndrome related diseases	H01731	http://www.geneontology.org/formats/oboInOwl#hasDbXref	脆弱X随伴振戦／失調症候群	Fragile X tremor/ataxia syndrome	https://identifiers.org/kegg.disease:H01731
NANDO:1200693	http://nanbyodata.jp/ontology/NANDO_1200693	総動脈幹遺残症	Truncus arteriosus communis	H01736	http://www.geneontology.org/formats/oboInOwl#hasDbXref	総動脈幹遺残症	Persistent truncus arteriosus	https://identifiers.org/kegg.disease:H01736
NANDO:1200698	http://nanbyodata.jp/ontology/NANDO_1200698	修正大血管転位症	Corrected transposition of great arteries	H01786	http://www.geneontology.org/formats/oboInOwl#hasDbXref	修正大血管転位症	Congenitally corrected transposition of the great arteries	https://identifiers.org/kegg.disease:H01786
NANDO:1200704	http://nanbyodata.jp/ontology/NANDO_1200704	単心室症	Single ventricle	H01787	http://www.geneontology.org/formats/oboInOwl#hasDbXref	単心室症	Univentricular heart	https://identifiers.org/kegg.disease:H01787
NANDO:1200706	http://nanbyodata.jp/ontology/NANDO_1200706	三尖弁閉鎖症	Tricuspid atresia	H01785	http://www.geneontology.org/formats/oboInOwl#hasDbXref	三尖弁閉鎖症	Tricuspid atresia	https://identifiers.org/kegg.disease:H01785
NANDO:1200707	http://nanbyodata.jp/ontology/NANDO_1200707	心室中隔欠損を伴わない肺動脈閉鎖症	Pulmonary atresia with intact ventricular septum	H01802	http://www.geneontology.org/formats/oboInOwl#hasDbXref	心室中隔欠損を伴わない肺動脈閉鎖症	Pulmonary atresia with intact ventricular septum	https://identifiers.org/kegg.disease:H01802
NANDO:1200708	http://nanbyodata.jp/ontology/NANDO_1200708	心室中隔欠損を伴う肺動脈閉鎖症	Pulmonary atresia with ventricular septal defect	H01803	http://www.geneontology.org/formats/oboInOwl#hasDbXref	心室中隔欠損を伴う肺動脈閉鎖症	Pulmonary atresia with ventricular septal defect	https://identifiers.org/kegg.disease:H01803
NANDO:1200711	http://nanbyodata.jp/ontology/NANDO_1200711	エプスタイン病	Ebstein's anomaly	H01783	http://www.geneontology.org/formats/oboInOwl#hasDbXref	エプスタイン病	Ebstein anomaly	https://identifiers.org/kegg.disease:H01783
NANDO:1200713	http://nanbyodata.jp/ontology/NANDO_1200713	ギャロウェイ・モワト症候群	Galloway-Mowat syndrome	H01722	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ギャロウェイ・モワト症候群	Galloway-Mowat syndrome	https://identifiers.org/kegg.disease:H01722
NANDO:1200718	http://nanbyodata.jp/ontology/NANDO_1200718	抗糸球体基底膜腎炎	Goodpasture syndrome	H01721	http://www.geneontology.org/formats/oboInOwl#hasDbXref	グッドパスチャー症候群	Goodpasture syndrome	https://identifiers.org/kegg.disease:H01721
NANDO:1200718	http://nanbyodata.jp/ontology/NANDO_1200718	抗糸球体基底膜腎炎	Goodpasture syndrome	H01721	http://www.geneontology.org/formats/oboInOwl#hasDbXref	抗糸球体基底膜腎炎	Goodpasture syndrome	https://identifiers.org/kegg.disease:H01721
NANDO:1200718	http://nanbyodata.jp/ontology/NANDO_1200718	抗糸球体基底膜腎炎	Goodpasture syndrome	H01721	http://www.geneontology.org/formats/oboInOwl#hasDbXref	グッドパスチャー症候群	Anti-glomerular basement membrane (GBM) disease	https://identifiers.org/kegg.disease:H01721
NANDO:1200718	http://nanbyodata.jp/ontology/NANDO_1200718	抗糸球体基底膜腎炎	Goodpasture syndrome	H01721	http://www.geneontology.org/formats/oboInOwl#hasDbXref	抗糸球体基底膜腎炎	Anti-glomerular basement membrane (GBM) disease	https://identifiers.org/kegg.disease:H01721
NANDO:1200741	http://nanbyodata.jp/ontology/NANDO_1200741	紫斑病性腎炎	Henoch-Schonlein purpura nephritis	H01767	http://www.geneontology.org/formats/oboInOwl#hasDbXref	紫斑病性腎炎	Henoch-Schonlein purpura nephritis	https://identifiers.org/kegg.disease:H01767
NANDO:1200745	http://nanbyodata.jp/ontology/NANDO_1200745	閉塞性細気管支炎	Bronchiolitis obliterans	H01873	http://www.geneontology.org/formats/oboInOwl#hasDbXref	閉塞性細気管支炎	Bronchiolitis obliterans	https://identifiers.org/kegg.disease:H01873
NANDO:1200745	http://nanbyodata.jp/ontology/NANDO_1200745	閉塞性細気管支炎	Bronchiolitis obliterans	H01873	http://www.geneontology.org/formats/oboInOwl#hasDbXref	閉塞性細気管支炎	Obliterative bronchiolitis	https://identifiers.org/kegg.disease:H01873
NANDO:1200752	http://nanbyodata.jp/ontology/NANDO_1200752	肥満低換気症候群	Obesity hypoventilation syndrome	H01715	http://www.geneontology.org/formats/oboInOwl#hasDbXref	肥満低換気症候群	Obesity hypoventilation syndrome	https://identifiers.org/kegg.disease:H01715
NANDO:1200752	http://nanbyodata.jp/ontology/NANDO_1200752	肥満低換気症候群	Obesity hypoventilation syndrome	H01715	http://www.geneontology.org/formats/oboInOwl#hasDbXref	肥満低換気症候群	Pickwickian Syndrome	https://identifiers.org/kegg.disease:H01715
NANDO:1200756	http://nanbyodata.jp/ontology/NANDO_1200756	カーニー複合	Carney complex	H01820	http://www.geneontology.org/formats/oboInOwl#hasDbXref	カーニー複合	Carney complex	https://identifiers.org/kegg.disease:H01820
NANDO:1200766	http://nanbyodata.jp/ontology/NANDO_1200766	D-二頭酵素欠損症	D-bifunctional protein deficiency	H02098	http://www.geneontology.org/formats/oboInOwl#hasDbXref	D-二頭酵素欠損症	D-bifunctional protein deficiency	https://identifiers.org/kegg.disease:H02098
NANDO:1200766	http://nanbyodata.jp/ontology/NANDO_1200766	D-二頭酵素欠損症	D-bifunctional protein deficiency	H02098	http://www.geneontology.org/formats/oboInOwl#hasDbXref	DBP 欠損症	D-bifunctional protein deficiency	https://identifiers.org/kegg.disease:H02098
NANDO:1200766	http://nanbyodata.jp/ontology/NANDO_1200766	D-二頭酵素欠損症	D-bifunctional protein deficiency	H02098	http://www.geneontology.org/formats/oboInOwl#hasDbXref	D-二頭酵素欠損症	Bifunctional enzyme deficiency	https://identifiers.org/kegg.disease:H02098
NANDO:1200766	http://nanbyodata.jp/ontology/NANDO_1200766	D-二頭酵素欠損症	D-bifunctional protein deficiency	H02098	http://www.geneontology.org/formats/oboInOwl#hasDbXref	DBP 欠損症	Bifunctional enzyme deficiency	https://identifiers.org/kegg.disease:H02098
NANDO:1200766	http://nanbyodata.jp/ontology/NANDO_1200766	D-二頭酵素欠損症	D-bifunctional protein deficiency	H02098	http://www.geneontology.org/formats/oboInOwl#hasDbXref	D-二頭酵素欠損症	DBP deficiency	https://identifiers.org/kegg.disease:H02098
NANDO:1200766	http://nanbyodata.jp/ontology/NANDO_1200766	D-二頭酵素欠損症	D-bifunctional protein deficiency	H02098	http://www.geneontology.org/formats/oboInOwl#hasDbXref	DBP 欠損症	DBP deficiency	https://identifiers.org/kegg.disease:H02098
NANDO:1200768	http://nanbyodata.jp/ontology/NANDO_1200768	２-メチルアシルCoAラセマーゼ欠損症	Alpha-methylacyl-CoA racemase deficiency	H02099	http://www.geneontology.org/formats/oboInOwl#hasDbXref	2-メチルアシルCoAラセマーゼ欠損症	Alpha-methylacyl-CoA racemase deficiency	https://identifiers.org/kegg.disease:H02099
NANDO:1200768	http://nanbyodata.jp/ontology/NANDO_1200768	２-メチルアシルCoAラセマーゼ欠損症	Alpha-methylacyl-CoA racemase deficiency	H02099	http://www.geneontology.org/formats/oboInOwl#hasDbXref	AMACR 欠損症	Alpha-methylacyl-CoA racemase deficiency	https://identifiers.org/kegg.disease:H02099
NANDO:1200768	http://nanbyodata.jp/ontology/NANDO_1200768	２-メチルアシルCoAラセマーゼ欠損症	Alpha-methylacyl-CoA racemase deficiency	H02099	http://www.geneontology.org/formats/oboInOwl#hasDbXref	2-メチルアシルCoAラセマーゼ欠損症	AMACR deficiency	https://identifiers.org/kegg.disease:H02099
NANDO:1200768	http://nanbyodata.jp/ontology/NANDO_1200768	２-メチルアシルCoAラセマーゼ欠損症	Alpha-methylacyl-CoA racemase deficiency	H02099	http://www.geneontology.org/formats/oboInOwl#hasDbXref	AMACR 欠損症	AMACR deficiency	https://identifiers.org/kegg.disease:H02099
NANDO:1200775	http://nanbyodata.jp/ontology/NANDO_1200775	副甲状腺機能低下症	Hypoparathyroidism	H01862	http://www.geneontology.org/formats/oboInOwl#hasDbXref	副甲状腺機能低下症	Hypoparathyroidism	https://identifiers.org/kegg.disease:H01862
NANDO:1200811	http://nanbyodata.jp/ontology/NANDO_1200811	ポルフィリン症	Porphyria	H01763	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ポルフィリン症	Porphyria	https://identifiers.org/kegg.disease:H01763
NANDO:1200823	http://nanbyodata.jp/ontology/NANDO_1200823	筋型糖原病	Muscle glycogen storage disease	H01762	http://www.geneontology.org/formats/oboInOwl#hasDbXref	筋型糖原病	Muscle glycogen storage disease	https://identifiers.org/kegg.disease:H01762
NANDO:1200838	http://nanbyodata.jp/ontology/NANDO_1200838	肝型糖原病	Hepatic glycogen storage disease	H01760	http://www.geneontology.org/formats/oboInOwl#hasDbXref	肝型糖原病	Hepatic glycogen storage disease	https://identifiers.org/kegg.disease:H01760
NANDO:1200851	http://nanbyodata.jp/ontology/NANDO_1200851	ガラクトース-1-リン酸ウリジルトランスフェラーゼ欠損症	Galactose-1-phosphate uridyltransferase deficiency	H02008	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ガラクトース-1-リン酸ウリジルトランスフェラーゼ欠損症	Classic galactosemia	https://identifiers.org/kegg.disease:H02008
NANDO:1200851	http://nanbyodata.jp/ontology/NANDO_1200851	ガラクトース-1-リン酸ウリジルトランスフェラーゼ欠損症	Galactose-1-phosphate uridyltransferase deficiency	H02008	http://www.geneontology.org/formats/oboInOwl#hasDbXref	古典型ガラクトース血症	Classic galactosemia	https://identifiers.org/kegg.disease:H02008
NANDO:1200851	http://nanbyodata.jp/ontology/NANDO_1200851	ガラクトース-1-リン酸ウリジルトランスフェラーゼ欠損症	Galactose-1-phosphate uridyltransferase deficiency	H02008	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ガラクトース血症 I 型	Classic galactosemia	https://identifiers.org/kegg.disease:H02008
NANDO:1200851	http://nanbyodata.jp/ontology/NANDO_1200851	ガラクトース-1-リン酸ウリジルトランスフェラーゼ欠損症	Galactose-1-phosphate uridyltransferase deficiency	H02008	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ガラクトース-1-リン酸ウリジルトランスフェラーゼ欠損症	Galactose-1P uridylyltransferase deficiency	https://identifiers.org/kegg.disease:H02008
NANDO:1200851	http://nanbyodata.jp/ontology/NANDO_1200851	ガラクトース-1-リン酸ウリジルトランスフェラーゼ欠損症	Galactose-1-phosphate uridyltransferase deficiency	H02008	http://www.geneontology.org/formats/oboInOwl#hasDbXref	古典型ガラクトース血症	Galactose-1P uridylyltransferase deficiency	https://identifiers.org/kegg.disease:H02008
NANDO:1200851	http://nanbyodata.jp/ontology/NANDO_1200851	ガラクトース-1-リン酸ウリジルトランスフェラーゼ欠損症	Galactose-1-phosphate uridyltransferase deficiency	H02008	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ガラクトース血症 I 型	Galactose-1P uridylyltransferase deficiency	https://identifiers.org/kegg.disease:H02008
NANDO:1200851	http://nanbyodata.jp/ontology/NANDO_1200851	ガラクトース-1-リン酸ウリジルトランスフェラーゼ欠損症	Galactose-1-phosphate uridyltransferase deficiency	H02008	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ガラクトース-1-リン酸ウリジルトランスフェラーゼ欠損症	Galactosemia type I	https://identifiers.org/kegg.disease:H02008
NANDO:1200851	http://nanbyodata.jp/ontology/NANDO_1200851	ガラクトース-1-リン酸ウリジルトランスフェラーゼ欠損症	Galactose-1-phosphate uridyltransferase deficiency	H02008	http://www.geneontology.org/formats/oboInOwl#hasDbXref	古典型ガラクトース血症	Galactosemia type I	https://identifiers.org/kegg.disease:H02008
NANDO:1200851	http://nanbyodata.jp/ontology/NANDO_1200851	ガラクトース-1-リン酸ウリジルトランスフェラーゼ欠損症	Galactose-1-phosphate uridyltransferase deficiency	H02008	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ガラクトース血症 I 型	Galactosemia type I	https://identifiers.org/kegg.disease:H02008
NANDO:1200855	http://nanbyodata.jp/ontology/NANDO_1200855	原発性高カイロミクロン血症	Primary hyperchylomicronemia	H01784	http://www.geneontology.org/formats/oboInOwl#hasDbXref	原発性高カイロミクロン血症	Primary hyperchylomicronemia	https://identifiers.org/kegg.disease:H01784
NANDO:1200872	http://nanbyodata.jp/ontology/NANDO_1200872	肋骨異常を伴う先天性側弯症	Congenital scoliosis with rib anomalies	H01851	http://www.geneontology.org/formats/oboInOwl#hasDbXref	肋骨異常を伴う先天性側弯症	Congenital scoliosis associated with rib anomalies	https://identifiers.org/kegg.disease:H01851
NANDO:1200874	http://nanbyodata.jp/ontology/NANDO_1200874	タナトフォリック骨異形成症	Thanatophoric dysplasia	H01750	http://www.geneontology.org/formats/oboInOwl#hasDbXref	タナトフォリック骨異形成症	Thanatophoric dysplasia	https://identifiers.org/kegg.disease:H01750
NANDO:1200877	http://nanbyodata.jp/ontology/NANDO_1200877	軟骨無形成症	Achondroplasia	H01749	http://www.geneontology.org/formats/oboInOwl#hasDbXref	軟骨無形成症	Achondroplasia	https://identifiers.org/kegg.disease:H01749
NANDO:1200884	http://nanbyodata.jp/ontology/NANDO_1200884	クリッペル・トレノネー・ウェーバー症候群	Klippel-Trenaunay-Weber syndrome	H01788	http://www.geneontology.org/formats/oboInOwl#hasDbXref	クリッペル・トレノネー・ウェーバー症候群	Klippel-Trenaunay-Weber syndrome	https://identifiers.org/kegg.disease:H01788
NANDO:1200890	http://nanbyodata.jp/ontology/NANDO_1200890	ダイアモンド・ブラックファン貧血	Diamond-Blackfan anemia	H00237	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ダイアモンド・ブラックファン貧血	Diamond-Blackfan anemia	https://identifiers.org/kegg.disease:H00237
NANDO:1200891	http://nanbyodata.jp/ontology/NANDO_1200891	ファンコニ貧血	Fanconi anemia	H00238	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ファンコニ貧血	Fanconi anemia	https://identifiers.org/kegg.disease:H00238
NANDO:1200892	http://nanbyodata.jp/ontology/NANDO_1200892	遺伝性鉄芽球性貧血	Hereditary sideroblastic anemia	H00982	http://www.geneontology.org/formats/oboInOwl#hasDbXref	遺伝性鉄芽球性貧血	Sideroblastic anemia	https://identifiers.org/kegg.disease:H00982
NANDO:1200893	http://nanbyodata.jp/ontology/NANDO_1200893	エプスタイン症候群	Epstein syndrome	H00578	http://www.geneontology.org/formats/oboInOwl#hasDbXref	エプスタイン症候群	Epstein syndrome	https://identifiers.org/kegg.disease:H00578
NANDO:1200897	http://nanbyodata.jp/ontology/NANDO_1200897	自己免疫性後天性凝固第 XIII/13 因子欠乏症	Autoimmune hemorrhaphilia XIII/13	H01759	http://www.geneontology.org/formats/oboInOwl#hasDbXref	自己免疫性出血病 XIII	Autoimmune hemorrhaphilia XIII/13	https://identifiers.org/kegg.disease:H01759
NANDO:1200897	http://nanbyodata.jp/ontology/NANDO_1200897	自己免疫性後天性凝固第 XIII/13 因子欠乏症	Autoimmune hemorrhaphilia XIII/13	H01759	http://www.geneontology.org/formats/oboInOwl#hasDbXref	自己免疫性後天性凝固第13因子欠乏症	Autoimmune hemorrhaphilia XIII/13	https://identifiers.org/kegg.disease:H01759
NANDO:1200897	http://nanbyodata.jp/ontology/NANDO_1200897	自己免疫性後天性凝固第 XIII/13 因子欠乏症	Autoimmune hemorrhaphilia XIII/13	H01759	http://www.geneontology.org/formats/oboInOwl#hasDbXref	自己免疫性出血病 XIII	Autoimmune acquired factor XIII (F13) deficiency	https://identifiers.org/kegg.disease:H01759
NANDO:1200897	http://nanbyodata.jp/ontology/NANDO_1200897	自己免疫性後天性凝固第 XIII/13 因子欠乏症	Autoimmune hemorrhaphilia XIII/13	H01759	http://www.geneontology.org/formats/oboInOwl#hasDbXref	自己免疫性後天性凝固第13因子欠乏症	Autoimmune acquired factor XIII (F13) deficiency	https://identifiers.org/kegg.disease:H01759
NANDO:1200902	http://nanbyodata.jp/ontology/NANDO_1200902	非特異性多発性小腸潰瘍症	Chronic nonspecific multiple ulcers of the small intestine	H01853	http://www.geneontology.org/formats/oboInOwl#hasDbXref	非特異性多発性小腸潰瘍症	Chronic nonspecific multiple ulcers of the small intestine	https://identifiers.org/kegg.disease:H01853
NANDO:1200903	http://nanbyodata.jp/ontology/NANDO_1200903	ヒルシュスプルング病	Hirschsprung disease	H00910	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ヒルシュスプルング病	Hirschsprung disease	https://identifiers.org/kegg.disease:H00910
NANDO:1200909	http://nanbyodata.jp/ontology/NANDO_1200909	総排泄腔外反症	Cloacal exstrophy	H01856	http://www.geneontology.org/formats/oboInOwl#hasDbXref	総排泄腔外反症	Cloacal exstrophy	https://identifiers.org/kegg.disease:H01856
NANDO:1200909	http://nanbyodata.jp/ontology/NANDO_1200909	総排泄腔外反症	Cloacal exstrophy	H01856	http://www.geneontology.org/formats/oboInOwl#hasDbXref	膀胱腸裂	Cloacal exstrophy	https://identifiers.org/kegg.disease:H01856
NANDO:1200909	http://nanbyodata.jp/ontology/NANDO_1200909	総排泄腔外反症	Cloacal exstrophy	H01856	http://www.geneontology.org/formats/oboInOwl#hasDbXref	総排泄腔外反症	Vesicointestinal fissure	https://identifiers.org/kegg.disease:H01856
NANDO:1200909	http://nanbyodata.jp/ontology/NANDO_1200909	総排泄腔外反症	Cloacal exstrophy	H01856	http://www.geneontology.org/formats/oboInOwl#hasDbXref	膀胱腸裂	Vesicointestinal fissure	https://identifiers.org/kegg.disease:H01856
NANDO:1200910	http://nanbyodata.jp/ontology/NANDO_1200910	総排泄腔遺残	Persistent cloaca	H01858	http://www.geneontology.org/formats/oboInOwl#hasDbXref	総排泄腔遺残	Persistent cloaca	https://identifiers.org/kegg.disease:H01858
NANDO:1200911	http://nanbyodata.jp/ontology/NANDO_1200911	先天性横隔膜ヘルニア	Congenital diaphragmatic hernia	H01241	http://www.geneontology.org/formats/oboInOwl#hasDbXref	先天性横隔膜ヘルニア	Congenital diaphragmatic hernia	https://identifiers.org/kegg.disease:H01241
NANDO:1200913	http://nanbyodata.jp/ontology/NANDO_1200913	胆道閉鎖症	Biliary atresia	H01855	http://www.geneontology.org/formats/oboInOwl#hasDbXref	胆道閉鎖症	Biliary atresia	https://identifiers.org/kegg.disease:H01855
NANDO:1200918	http://nanbyodata.jp/ontology/NANDO_1200918	アラジール症候群	Alagille syndrome	H00551	http://www.geneontology.org/formats/oboInOwl#hasDbXref	アラジール症候群	Alagille syndrome	https://identifiers.org/kegg.disease:H00551
NANDO:1200921	http://nanbyodata.jp/ontology/NANDO_1200921	遺伝性膵炎	Hereditary pancreatitis	H00933	http://www.geneontology.org/formats/oboInOwl#hasDbXref	遺伝性膵炎	Hereditary pancreatitis	https://identifiers.org/kegg.disease:H00933
NANDO:1200921	http://nanbyodata.jp/ontology/NANDO_1200921	遺伝性膵炎	Hereditary pancreatitis	H00933	http://www.geneontology.org/formats/oboInOwl#hasDbXref	遺伝性膵炎	Hereditary chronic pancreatitis	https://identifiers.org/kegg.disease:H00933
NANDO:1200922	http://nanbyodata.jp/ontology/NANDO_1200922	嚢胞性線維症	Cystic fibrosis	H00218	http://www.geneontology.org/formats/oboInOwl#hasDbXref	嚢胞性線維症	Cystic fibrosis	https://identifiers.org/kegg.disease:H00218
NANDO:1200931	http://nanbyodata.jp/ontology/NANDO_1200931	黄斑ジストロフィー	Macular dystrophy	H01770	http://www.geneontology.org/formats/oboInOwl#hasDbXref	黄斑ジストロフィー	Macular dystrophy	https://identifiers.org/kegg.disease:H01770
NANDO:1200932	http://nanbyodata.jp/ontology/NANDO_1200932	卵黄様黄斑ジストロフィー	Vitelliform macular dystrophy	H00814	http://www.geneontology.org/formats/oboInOwl#hasDbXref	卵黄状黄斑ジストロフィー	Vitelliform macular dystrophy	https://identifiers.org/kegg.disease:H00814
NANDO:1200933	http://nanbyodata.jp/ontology/NANDO_1200933	Stargardt病	Stargardt disease	H00819	http://www.geneontology.org/formats/oboInOwl#hasDbXref	シュタルガルト病	Stargardt disease	https://identifiers.org/kegg.disease:H00819
NANDO:1200933	http://nanbyodata.jp/ontology/NANDO_1200933	Stargardt病	Stargardt disease	H00819	http://www.geneontology.org/formats/oboInOwl#hasDbXref	シュタルガルト病	Fundus flavimaculatus	https://identifiers.org/kegg.disease:H00819
NANDO:1200934	http://nanbyodata.jp/ontology/NANDO_1200934	オカルト黄斑ジストロフィー	Occult macular dystrophy	H01010	http://www.geneontology.org/formats/oboInOwl#hasDbXref	オカルト黄斑ジストロフィー	Occult macular dystrophy	https://identifiers.org/kegg.disease:H01010
NANDO:1200935	http://nanbyodata.jp/ontology/NANDO_1200935	錐体ジストロフィー、および錐体杆体ジストロフィー	Cone-rod dystrophy and cone dystrophy	H00481	http://www.geneontology.org/formats/oboInOwl#hasDbXref	錐体杆体ジストロフィおよび錐体ジストロフィー	Cone-rod dystrophy and cone dystrophy	https://identifiers.org/kegg.disease:H00481
NANDO:1200939	http://nanbyodata.jp/ontology/NANDO_1200939	中心性輪紋状脈絡膜ジストロフィー	Central areolar choroidal dystrophy	H01768	http://www.geneontology.org/formats/oboInOwl#hasDbXref	中心性輪紋状脈絡膜ジストロフィー	Central areolar choroidal dystrophy	https://identifiers.org/kegg.disease:H01768
NANDO:1200940	http://nanbyodata.jp/ontology/NANDO_1200940	レーベル遺伝性視神経症	Leber hereditary optic neuropathy	H00068	http://www.geneontology.org/formats/oboInOwl#hasDbXref	レーベル遺伝性視神経症	Leber optic atrophy	https://identifiers.org/kegg.disease:H00068
NANDO:1200940	http://nanbyodata.jp/ontology/NANDO_1200940	レーベル遺伝性視神経症	Leber hereditary optic neuropathy	H00068	http://www.geneontology.org/formats/oboInOwl#hasDbXref	レーバー遺伝性視神経萎縮症	Leber optic atrophy	https://identifiers.org/kegg.disease:H00068
NANDO:1200940	http://nanbyodata.jp/ontology/NANDO_1200940	レーベル遺伝性視神経症	Leber hereditary optic neuropathy	H00068	http://www.geneontology.org/formats/oboInOwl#hasDbXref	レーベル遺伝性視神経症	Leber hereditary optic atrophy	https://identifiers.org/kegg.disease:H00068
NANDO:1200940	http://nanbyodata.jp/ontology/NANDO_1200940	レーベル遺伝性視神経症	Leber hereditary optic neuropathy	H00068	http://www.geneontology.org/formats/oboInOwl#hasDbXref	レーバー遺伝性視神経萎縮症	Leber hereditary optic atrophy	https://identifiers.org/kegg.disease:H00068
NANDO:1200941	http://nanbyodata.jp/ontology/NANDO_1200941	アッシャー症候群	Usher syndrome	H00779	http://www.geneontology.org/formats/oboInOwl#hasDbXref	アッシャー症候群	Usher syndrome	https://identifiers.org/kegg.disease:H00779
NANDO:1200945	http://nanbyodata.jp/ontology/NANDO_1200945	若年発症型両側性感音難聴	Juvenile bilateral sensorineural hearing loss	H01705	http://www.geneontology.org/formats/oboInOwl#hasDbXref	若年発症型両側性感音難聴	Bilateral sudden sensorineural hearing loss	https://identifiers.org/kegg.disease:H01705
NANDO:1200945	http://nanbyodata.jp/ontology/NANDO_1200945	若年発症型両側性感音難聴	Juvenile bilateral sensorineural hearing loss	H01705	http://www.geneontology.org/formats/oboInOwl#hasDbXref	突発性両側性感音難聴	Bilateral sudden sensorineural hearing loss	https://identifiers.org/kegg.disease:H01705
NANDO:1200946	http://nanbyodata.jp/ontology/NANDO_1200946	遅発性内リンパ水腫	Delayed endolymphatic hydrops	H01706	http://www.geneontology.org/formats/oboInOwl#hasDbXref	遅発性内リンパ水腫	Delayed endolymphatic hydrops	https://identifiers.org/kegg.disease:H01706
NANDO:1200947	http://nanbyodata.jp/ontology/NANDO_1200947	好酸球性副鼻腔炎	Eosinophilic sinusitis	H01765	http://www.geneontology.org/formats/oboInOwl#hasDbXref	好酸球性副鼻腔炎	Eosinophilic sinusitis	https://identifiers.org/kegg.disease:H01765
NANDO:1200947	http://nanbyodata.jp/ontology/NANDO_1200947	好酸球性副鼻腔炎	Eosinophilic sinusitis	H01765	http://www.geneontology.org/formats/oboInOwl#hasDbXref	好酸球性副鼻腔炎	Eosinophilic chronic rhinosinusitis	https://identifiers.org/kegg.disease:H01765
NANDO:1200948	http://nanbyodata.jp/ontology/NANDO_1200948	カナバン病	Canavan disease	H00074	http://www.geneontology.org/formats/oboInOwl#hasDbXref	カナバン病	Canavan disease	https://identifiers.org/kegg.disease:H00074
NANDO:1200950	http://nanbyodata.jp/ontology/NANDO_1200950	皮質下嚢胞をもつ大頭型白質脳症	Megaloencephalic leukoencephalopathy with subcortical cysts	H00875	http://www.geneontology.org/formats/oboInOwl#hasDbXref	皮質下嚢胞をもつ大頭型白質脳症	Megaloencephalic leukoencephalopathy with subcortical cysts	https://identifiers.org/kegg.disease:H00875
NANDO:1200951	http://nanbyodata.jp/ontology/NANDO_1200951	白質消失病	Vanishing white matter disease	H00869	http://www.geneontology.org/formats/oboInOwl#hasDbXref	白質消失病	Vanishing white matter disease	https://identifiers.org/kegg.disease:H00869
NANDO:1200951	http://nanbyodata.jp/ontology/NANDO_1200951	白質消失病	Vanishing white matter disease	H00869	http://www.geneontology.org/formats/oboInOwl#hasDbXref	Cree 白質脳症	Vanishing white matter disease	https://identifiers.org/kegg.disease:H00869
NANDO:1200951	http://nanbyodata.jp/ontology/NANDO_1200951	白質消失病	Vanishing white matter disease	H00869	http://www.geneontology.org/formats/oboInOwl#hasDbXref	VWM 型白質脳症	Vanishing white matter disease	https://identifiers.org/kegg.disease:H00869
NANDO:1200951	http://nanbyodata.jp/ontology/NANDO_1200951	白質消失病	Vanishing white matter disease	H00869	http://www.geneontology.org/formats/oboInOwl#hasDbXref	中枢神経系白質形成不全症を伴う小児失調症	Vanishing white matter disease	https://identifiers.org/kegg.disease:H00869
NANDO:1200951	http://nanbyodata.jp/ontology/NANDO_1200951	白質消失病	Vanishing white matter disease	H00869	http://www.geneontology.org/formats/oboInOwl#hasDbXref	白質消失病	Leukoencephalopathy with vanishing white matter	https://identifiers.org/kegg.disease:H00869
NANDO:1200951	http://nanbyodata.jp/ontology/NANDO_1200951	白質消失病	Vanishing white matter disease	H00869	http://www.geneontology.org/formats/oboInOwl#hasDbXref	Cree 白質脳症	Leukoencephalopathy with vanishing white matter	https://identifiers.org/kegg.disease:H00869
NANDO:1200951	http://nanbyodata.jp/ontology/NANDO_1200951	白質消失病	Vanishing white matter disease	H00869	http://www.geneontology.org/formats/oboInOwl#hasDbXref	VWM 型白質脳症	Leukoencephalopathy with vanishing white matter	https://identifiers.org/kegg.disease:H00869
NANDO:1200951	http://nanbyodata.jp/ontology/NANDO_1200951	白質消失病	Vanishing white matter disease	H00869	http://www.geneontology.org/formats/oboInOwl#hasDbXref	中枢神経系白質形成不全症を伴う小児失調症	Leukoencephalopathy with vanishing white matter	https://identifiers.org/kegg.disease:H00869
NANDO:1200951	http://nanbyodata.jp/ontology/NANDO_1200951	白質消失病	Vanishing white matter disease	H00869	http://www.geneontology.org/formats/oboInOwl#hasDbXref	白質消失病	Cree leukoencephalopathy (CLE)	https://identifiers.org/kegg.disease:H00869
NANDO:1200951	http://nanbyodata.jp/ontology/NANDO_1200951	白質消失病	Vanishing white matter disease	H00869	http://www.geneontology.org/formats/oboInOwl#hasDbXref	Cree 白質脳症	Cree leukoencephalopathy (CLE)	https://identifiers.org/kegg.disease:H00869
NANDO:1200951	http://nanbyodata.jp/ontology/NANDO_1200951	白質消失病	Vanishing white matter disease	H00869	http://www.geneontology.org/formats/oboInOwl#hasDbXref	VWM 型白質脳症	Cree leukoencephalopathy (CLE)	https://identifiers.org/kegg.disease:H00869
NANDO:1200951	http://nanbyodata.jp/ontology/NANDO_1200951	白質消失病	Vanishing white matter disease	H00869	http://www.geneontology.org/formats/oboInOwl#hasDbXref	中枢神経系白質形成不全症を伴う小児失調症	Cree leukoencephalopathy (CLE)	https://identifiers.org/kegg.disease:H00869
NANDO:1200951	http://nanbyodata.jp/ontology/NANDO_1200951	白質消失病	Vanishing white matter disease	H00869	http://www.geneontology.org/formats/oboInOwl#hasDbXref	白質消失病	Childhood ataxia with diffuse central nervous system hypomyelination (CACH)	https://identifiers.org/kegg.disease:H00869
NANDO:1200951	http://nanbyodata.jp/ontology/NANDO_1200951	白質消失病	Vanishing white matter disease	H00869	http://www.geneontology.org/formats/oboInOwl#hasDbXref	Cree 白質脳症	Childhood ataxia with diffuse central nervous system hypomyelination (CACH)	https://identifiers.org/kegg.disease:H00869
NANDO:1200951	http://nanbyodata.jp/ontology/NANDO_1200951	白質消失病	Vanishing white matter disease	H00869	http://www.geneontology.org/formats/oboInOwl#hasDbXref	VWM 型白質脳症	Childhood ataxia with diffuse central nervous system hypomyelination (CACH)	https://identifiers.org/kegg.disease:H00869
NANDO:1200951	http://nanbyodata.jp/ontology/NANDO_1200951	白質消失病	Vanishing white matter disease	H00869	http://www.geneontology.org/formats/oboInOwl#hasDbXref	中枢神経系白質形成不全症を伴う小児失調症	Childhood ataxia with diffuse central nervous system hypomyelination (CACH)	https://identifiers.org/kegg.disease:H00869
NANDO:1200953	http://nanbyodata.jp/ontology/NANDO_1200953	進行性ミオクローヌスてんかん	Progressive myoclonus epilepsy	H00810	http://www.geneontology.org/formats/oboInOwl#hasDbXref	進行性ミオクローヌスてんかん	Progressive myoclonic epilepsy	https://identifiers.org/kegg.disease:H00810
NANDO:1200959	http://nanbyodata.jp/ontology/NANDO_1200959	9q34欠失症候群	9q34 deletion syndrome	H00907	http://www.geneontology.org/formats/oboInOwl#hasDbXref	9q34欠失症候群	Kleefstra syndrome	https://identifiers.org/kegg.disease:H00907
NANDO:1200959	http://nanbyodata.jp/ontology/NANDO_1200959	9q34欠失症候群	9q34 deletion syndrome	H00907	http://www.geneontology.org/formats/oboInOwl#hasDbXref	9qサブテロメリア欠失症候群	Kleefstra syndrome	https://identifiers.org/kegg.disease:H00907
NANDO:1200959	http://nanbyodata.jp/ontology/NANDO_1200959	9q34欠失症候群	9q34 deletion syndrome	H00907	http://www.geneontology.org/formats/oboInOwl#hasDbXref	Kleefstra 症候群	Kleefstra syndrome	https://identifiers.org/kegg.disease:H00907
NANDO:1200959	http://nanbyodata.jp/ontology/NANDO_1200959	9q34欠失症候群	9q34 deletion syndrome	H00907	http://www.geneontology.org/formats/oboInOwl#hasDbXref	9q34欠失症候群	9q Subtelomeric deletion syndrome	https://identifiers.org/kegg.disease:H00907
NANDO:1200959	http://nanbyodata.jp/ontology/NANDO_1200959	9q34欠失症候群	9q34 deletion syndrome	H00907	http://www.geneontology.org/formats/oboInOwl#hasDbXref	9qサブテロメリア欠失症候群	9q Subtelomeric deletion syndrome	https://identifiers.org/kegg.disease:H00907
NANDO:1200959	http://nanbyodata.jp/ontology/NANDO_1200959	9q34欠失症候群	9q34 deletion syndrome	H00907	http://www.geneontology.org/formats/oboInOwl#hasDbXref	Kleefstra 症候群	9q Subtelomeric deletion syndrome	https://identifiers.org/kegg.disease:H00907
NANDO:1200959	http://nanbyodata.jp/ontology/NANDO_1200959	9q34欠失症候群	9q34 deletion syndrome	H00907	http://www.geneontology.org/formats/oboInOwl#hasDbXref	9q34欠失症候群	Chromosome 9q34.3 deletion syndrome	https://identifiers.org/kegg.disease:H00907
NANDO:1200959	http://nanbyodata.jp/ontology/NANDO_1200959	9q34欠失症候群	9q34 deletion syndrome	H00907	http://www.geneontology.org/formats/oboInOwl#hasDbXref	9qサブテロメリア欠失症候群	Chromosome 9q34.3 deletion syndrome	https://identifiers.org/kegg.disease:H00907
NANDO:1200959	http://nanbyodata.jp/ontology/NANDO_1200959	9q34欠失症候群	9q34 deletion syndrome	H00907	http://www.geneontology.org/formats/oboInOwl#hasDbXref	Kleefstra 症候群	Chromosome 9q34.3 deletion syndrome	https://identifiers.org/kegg.disease:H00907
NANDO:1200960	http://nanbyodata.jp/ontology/NANDO_1200960	コルネリア・デランゲ症候群	Cornelia de lange syndrome	H00631	http://www.geneontology.org/formats/oboInOwl#hasDbXref	コルネリア・デランゲ症候群	Cornelia de Lange syndrome	https://identifiers.org/kegg.disease:H00631
NANDO:1200961	http://nanbyodata.jp/ontology/NANDO_1200961	スミス・レムリ・オピッツ症候群	Smith-lemli-opitz syndrome	H00161	http://www.geneontology.org/formats/oboInOwl#hasDbXref	スミス・レムリ・オピッツ症候群	Smith-Lemli-Opitz syndrome	https://identifiers.org/kegg.disease:H00161
NANDO:1200963	http://nanbyodata.jp/ontology/NANDO_1200963	先天性僧帽弁狭窄症	Congenital mitral stenosis	H02603	http://www.geneontology.org/formats/oboInOwl#hasDbXref	先天性僧帽弁狭窄症	Congenital mitral valve stenosis	https://identifiers.org/kegg.disease:H02603
NANDO:1200967	http://nanbyodata.jp/ontology/NANDO_1200967	ネイル・パテラ症候群	Nail-patella syndrome	H00464	http://www.geneontology.org/formats/oboInOwl#hasDbXref	爪膝蓋骨症候群	Nail-patella syndrome	https://identifiers.org/kegg.disease:H00464
NANDO:1200973	http://nanbyodata.jp/ontology/NANDO_1200973	カルニチントランスポーター欠損症	Systemic primary carnitine deficiency	H01589	http://www.geneontology.org/formats/oboInOwl#hasDbXref	全身性カルニチン欠乏症	Systemic primary carnitine deficiency	https://identifiers.org/kegg.disease:H01589
NANDO:1200974	http://nanbyodata.jp/ontology/NANDO_1200974	三頭酵素欠損症	Trifunctional protein deficiency	H01352	http://www.geneontology.org/formats/oboInOwl#hasDbXref	三頭酵素欠損症	Mitochondrial trifunctional protein deficiency	https://identifiers.org/kegg.disease:H01352
NANDO:1200984	http://nanbyodata.jp/ontology/NANDO_1200984	非ケトーシス型高グリシン血症	Nonketotic hyperglycinemia	H00191	http://www.geneontology.org/formats/oboInOwl#hasDbXref	非ケトーシス型高グリシン血症	Nonketotic hyperglycinemia	https://identifiers.org/kegg.disease:H00191
NANDO:1200984	http://nanbyodata.jp/ontology/NANDO_1200984	非ケトーシス型高グリシン血症	Nonketotic hyperglycinemia	H00191	http://www.geneontology.org/formats/oboInOwl#hasDbXref	グリシン脳症	Nonketotic hyperglycinemia	https://identifiers.org/kegg.disease:H00191
NANDO:1200984	http://nanbyodata.jp/ontology/NANDO_1200984	非ケトーシス型高グリシン血症	Nonketotic hyperglycinemia	H00191	http://www.geneontology.org/formats/oboInOwl#hasDbXref	非ケトーシス型高グリシン血症	Glycine encephalopathy (GCE)	https://identifiers.org/kegg.disease:H00191
NANDO:1200984	http://nanbyodata.jp/ontology/NANDO_1200984	非ケトーシス型高グリシン血症	Nonketotic hyperglycinemia	H00191	http://www.geneontology.org/formats/oboInOwl#hasDbXref	グリシン脳症	Glycine encephalopathy (GCE)	https://identifiers.org/kegg.disease:H00191
NANDO:1200987	http://nanbyodata.jp/ontology/NANDO_1200987	β-ケトチオラーゼ欠損症	Beta-ketothiolase deficiency	H01076	http://www.geneontology.org/formats/oboInOwl#hasDbXref	β-ケトチオラーゼ欠損症	Beta-ketothiolase deficiency	https://identifiers.org/kegg.disease:H01076
NANDO:1200987	http://nanbyodata.jp/ontology/NANDO_1200987	β-ケトチオラーゼ欠損症	Beta-ketothiolase deficiency	H01076	http://www.geneontology.org/formats/oboInOwl#hasDbXref	α-メチルアセト酢酸尿症	Beta-ketothiolase deficiency	https://identifiers.org/kegg.disease:H01076
NANDO:1200987	http://nanbyodata.jp/ontology/NANDO_1200987	β-ケトチオラーゼ欠損症	Beta-ketothiolase deficiency	H01076	http://www.geneontology.org/formats/oboInOwl#hasDbXref	β-ケトチオラーゼ欠損症	Alpha-methylacetoacetic aciduria	https://identifiers.org/kegg.disease:H01076
NANDO:1200987	http://nanbyodata.jp/ontology/NANDO_1200987	β-ケトチオラーゼ欠損症	Beta-ketothiolase deficiency	H01076	http://www.geneontology.org/formats/oboInOwl#hasDbXref	α-メチルアセト酢酸尿症	Alpha-methylacetoacetic aciduria	https://identifiers.org/kegg.disease:H01076
NANDO:1200988	http://nanbyodata.jp/ontology/NANDO_1200988	芳香族L－アミノ酸脱炭酸酵素欠損症	Aromatic L-amino acid decarboxylase deficiency	H01161	http://www.geneontology.org/formats/oboInOwl#hasDbXref	AADC欠損症	Aromatic L-amino acid decarboxylase deficiency	https://identifiers.org/kegg.disease:H01161
NANDO:1200988	http://nanbyodata.jp/ontology/NANDO_1200988	芳香族L－アミノ酸脱炭酸酵素欠損症	Aromatic L-amino acid decarboxylase deficiency	H01161	http://www.geneontology.org/formats/oboInOwl#hasDbXref	芳香族 L- アミノ酸脱炭酸酵素欠損症	Aromatic L-amino acid decarboxylase deficiency	https://identifiers.org/kegg.disease:H01161
NANDO:1200989	http://nanbyodata.jp/ontology/NANDO_1200989	メチルグルタコン酸尿症	Methylglutaconic aciduria	H00754	http://www.geneontology.org/formats/oboInOwl#hasDbXref	メチルグルタコン酸尿症	3-Methylglutaconic aciduria	https://identifiers.org/kegg.disease:H00754
NANDO:1200996	http://nanbyodata.jp/ontology/NANDO_1200996	エカルディ・グティエール症候群	Aicardi-Goutières Syndrome	H00290	http://www.geneontology.org/formats/oboInOwl#hasDbXref	エカルディ・グティエール症候群	Aicardi-Goutieres syndrome	https://identifiers.org/kegg.disease:H00290
NANDO:1200998	http://nanbyodata.jp/ontology/NANDO_1200998	大理石骨病	Osteopetrosis	H00436	http://www.geneontology.org/formats/oboInOwl#hasDbXref	大理石骨病	Osteopetrosis	https://identifiers.org/kegg.disease:H00436
NANDO:1201000	http://nanbyodata.jp/ontology/NANDO_1201000	前眼部形成異常	Anterior segment dysgenesis	H01159	http://www.geneontology.org/formats/oboInOwl#hasDbXref	前眼部形成異常	Anterior segment dysgenesis	https://identifiers.org/kegg.disease:H01159
NANDO:1201001	http://nanbyodata.jp/ontology/NANDO_1201001	無虹彩症	Aniridia	H00635	http://www.geneontology.org/formats/oboInOwl#hasDbXref	無虹彩症	Aniridia	https://identifiers.org/kegg.disease:H00635
NANDO:1201006	http://nanbyodata.jp/ontology/NANDO_1201006	膠様滴状角膜ジストロフィー	Gelatinous drop-like corneal dystrophy	H00953	http://www.geneontology.org/formats/oboInOwl#hasDbXref	膠様滴状角膜ジストロフィー	Gelatinous drop-like corneal dystrophy	https://identifiers.org/kegg.disease:H00953
NANDO:1201006	http://nanbyodata.jp/ontology/NANDO_1201006	膠様滴状角膜ジストロフィー	Gelatinous drop-like corneal dystrophy	H00953	http://www.geneontology.org/formats/oboInOwl#hasDbXref	角膜アミロイド症	Gelatinous drop-like corneal dystrophy	https://identifiers.org/kegg.disease:H00953
NANDO:1201006	http://nanbyodata.jp/ontology/NANDO_1201006	膠様滴状角膜ジストロフィー	Gelatinous drop-like corneal dystrophy	H00953	http://www.geneontology.org/formats/oboInOwl#hasDbXref	膠様滴状角膜ジストロフィー	Corneal amyloidosis	https://identifiers.org/kegg.disease:H00953
NANDO:1201006	http://nanbyodata.jp/ontology/NANDO_1201006	膠様滴状角膜ジストロフィー	Gelatinous drop-like corneal dystrophy	H00953	http://www.geneontology.org/formats/oboInOwl#hasDbXref	角膜アミロイド症	Corneal amyloidosis	https://identifiers.org/kegg.disease:H00953
NANDO:1201007	http://nanbyodata.jp/ontology/NANDO_1201007	ハッチンソン・ギルフォード症候群	Hutchinson-Gilford syndrome	H00601	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ハッチンソン・ギルフォード症候群	Hutchinson-Gilford progeria syndrome	https://identifiers.org/kegg.disease:H00601
NANDO:1201032	http://nanbyodata.jp/ontology/NANDO_1201032	脳クレアチン欠乏症候群	Cerebral creatine deficiency syndromes	H00849	http://www.geneontology.org/formats/oboInOwl#hasDbXref	脳クレアチン欠乏症候群	Cerebral creatine deficiency syndrome	https://identifiers.org/kegg.disease:H00849
NANDO:1201034	http://nanbyodata.jp/ontology/NANDO_1201034	グアニジノ酢酸メチル基転位酵素欠損症	Guanidinoacetate methyltransferase deficiency	H00834	http://www.geneontology.org/formats/oboInOwl#hasDbXref	グアニジノ酢酸メチルトランスフェラーゼ欠損症	Guanidinoacetate methyltransferase deficiency	https://identifiers.org/kegg.disease:H00834
NANDO:1201036	http://nanbyodata.jp/ontology/NANDO_1201036	ネフロン癆	Nephronophthisis	H00537	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ネフロン癆	Nephronophthisis	https://identifiers.org/kegg.disease:H00537
NANDO:1201038	http://nanbyodata.jp/ontology/NANDO_1201038	ホモシスチン尿症	Homocystinuria	H00183	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ホモシスチン尿症	Homocystinuria	https://identifiers.org/kegg.disease:H00183
NANDO:1201042	http://nanbyodata.jp/ontology/NANDO_1201042	進行性家族性肝内胆汁うっ滞症	Progressive familial intrahepatic cholestasis	H00624	http://www.geneontology.org/formats/oboInOwl#hasDbXref	進行性家族性肝内胆汁うっ滞症	Progressive familial intrahepatic cholestasis	https://identifiers.org/kegg.disease:H00624
NANDO:1201049	http://nanbyodata.jp/ontology/NANDO_1201049	セニオール・ローケン症候群	Senior-Loken syndrome	H00538	http://www.geneontology.org/formats/oboInOwl#hasDbXref	Senior-Loken 症候群	Senior-Loken syndrome	https://identifiers.org/kegg.disease:H00538
NANDO:1201050	http://nanbyodata.jp/ontology/NANDO_1201050	COACH症候群	COACH syndrome	H01001	http://www.geneontology.org/formats/oboInOwl#hasDbXref	COACH 症候群	COACH syndrome	https://identifiers.org/kegg.disease:H01001
NANDO:1201051	http://nanbyodata.jp/ontology/NANDO_1201051	口-顔-指症候群	Oral-facial-digital syndrome	H00454	http://www.geneontology.org/formats/oboInOwl#hasDbXref	Oral-facial-digital 症候群	Oral-facial-digital syndrome	https://identifiers.org/kegg.disease:H00454
NANDO:1201058	http://nanbyodata.jp/ontology/NANDO_1201058	ラパデリノ症候群	RAPADILINO syndrome	H00965	http://www.geneontology.org/formats/oboInOwl#hasDbXref	RAPADILINO 症候群	RAPADILINO syndrome	https://identifiers.org/kegg.disease:H00965
NANDO:1201064	http://nanbyodata.jp/ontology/NANDO_1201064	カーンズ・セイヤー症候群	Kearns-Sayre syndrome	H01355	http://www.geneontology.org/formats/oboInOwl#hasDbXref	カーンズ・セイアー症候群	Kearns-Sayre syndrome	https://identifiers.org/kegg.disease:H01355
NANDO:1201071	http://nanbyodata.jp/ontology/NANDO_1201071	多小脳回	Polymicrogyria	H00271	http://www.geneontology.org/formats/oboInOwl#hasDbXref	多小脳回	Polymicrogyria	https://identifiers.org/kegg.disease:H00271
NANDO:1201073	http://nanbyodata.jp/ontology/NANDO_1201073	裂脳症	Schizencephaly	H01160	http://www.geneontology.org/formats/oboInOwl#hasDbXref	裂脳症	Schizencephaly	https://identifiers.org/kegg.disease:H01160
NANDO:1201074	http://nanbyodata.jp/ontology/NANDO_1201074	孔脳症	Porencephaly	H00839	http://www.geneontology.org/formats/oboInOwl#hasDbXref	孔脳症	Porencephaly	https://identifiers.org/kegg.disease:H00839
NANDO:1201079	http://nanbyodata.jp/ontology/NANDO_1201079	脳室周囲結節状異所性灰白質	Periventricular nodular heterotopia	H00270	http://www.geneontology.org/formats/oboInOwl#hasDbXref	脳室周囲結節性異所性灰白質	Periventricular nodular heterotopia	https://identifiers.org/kegg.disease:H00270
NANDO:1201102	http://nanbyodata.jp/ontology/NANDO_1201102	短体幹症	Brachyolmia, autosomal dominant type	H00522	http://www.geneontology.org/formats/oboInOwl#hasDbXref	短体幹症	Brachyolmia	https://identifiers.org/kegg.disease:H00522
NANDO:2100003	http://nanbyodata.jp/ontology/NANDO_2100003	骨髄異形成症候群	Myelodysplastic syndrome	H01481	http://www.geneontology.org/formats/oboInOwl#hasDbXref	骨髄異形成症候群	Myelodysplastic syndrome	https://identifiers.org/kegg.disease:H01481
NANDO:2100009	http://nanbyodata.jp/ontology/NANDO_2100009	ネフローゼ症候群	Nephrotic syndrome	H01657	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ネフローゼ症候群	Nephrotic syndrome	https://identifiers.org/kegg.disease:H01657
NANDO:2100015	http://nanbyodata.jp/ontology/NANDO_2100015	ネフロン癆	Nephronophthisis	H00537	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ネフロン癆	Nephronophthisis	https://identifiers.org/kegg.disease:H00537
NANDO:2100020	http://nanbyodata.jp/ontology/NANDO_2100020	ギッテルマン症候群	Gitelman syndrome	H00240	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ギテルマン症候群	Gitelman syndrome	https://identifiers.org/kegg.disease:H00240
NANDO:2100021	http://nanbyodata.jp/ontology/NANDO_2100021	バーター症候群	Bartter syndrome	H00239	http://www.geneontology.org/formats/oboInOwl#hasDbXref	バーター症候群	Bartter syndrome	https://identifiers.org/kegg.disease:H00239
NANDO:2100028	http://nanbyodata.jp/ontology/NANDO_2100028	ロウ症候群	Lowe syndrome	H00692	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ロウ症候群	Lowe syndrome	https://identifiers.org/kegg.disease:H00692
NANDO:2100028	http://nanbyodata.jp/ontology/NANDO_2100028	ロウ症候群	Lowe syndrome	H00692	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ロウ症候群	Oculocerebrorenal Dystrophy (OCRL)	https://identifiers.org/kegg.disease:H00692
NANDO:2100032	http://nanbyodata.jp/ontology/NANDO_2100032	先天性中枢性低換気症候群	Congenital central hypoventilation syndrome	H00916	http://www.geneontology.org/formats/oboInOwl#hasDbXref	先天性中枢性低換気症候群	Congenital central hypoventilation syndrome	https://identifiers.org/kegg.disease:H00916
NANDO:2100035	http://nanbyodata.jp/ontology/NANDO_2100035	嚢胞性線維症	Cystic fibrosis	H00218	http://www.geneontology.org/formats/oboInOwl#hasDbXref	嚢胞性線維症	Cystic fibrosis	https://identifiers.org/kegg.disease:H00218
NANDO:2100036	http://nanbyodata.jp/ontology/NANDO_2100036	気管支拡張症	Bronchiectasis	H00892	http://www.geneontology.org/formats/oboInOwl#hasDbXref	気管支拡張症	Bronchiectasis with or without elevated sweat chloride	https://identifiers.org/kegg.disease:H00892
NANDO:2100039	http://nanbyodata.jp/ontology/NANDO_2100039	閉塞性細気管支炎	Bronchiolitis obliterans	H01873	http://www.geneontology.org/formats/oboInOwl#hasDbXref	閉塞性細気管支炎	Bronchiolitis obliterans	https://identifiers.org/kegg.disease:H01873
NANDO:2100040	http://nanbyodata.jp/ontology/NANDO_2100040	先天性横隔膜ヘルニア	Congenital diaphragmatic hernia	H01241	http://www.geneontology.org/formats/oboInOwl#hasDbXref	先天性横隔膜ヘルニア	Congenital diaphragmatic hernia	https://identifiers.org/kegg.disease:H01241
NANDO:2100043	http://nanbyodata.jp/ontology/NANDO_2100043	洞不全症候群	Sick sinus syndrome	H00729	http://www.geneontology.org/formats/oboInOwl#hasDbXref	洞不全症候群	Sick sinus syndrome	https://identifiers.org/kegg.disease:H00729
NANDO:2100043	http://nanbyodata.jp/ontology/NANDO_2100043	洞不全症候群	Sick sinus syndrome	H00729	http://www.geneontology.org/formats/oboInOwl#hasDbXref	洞不全症候群	Sinus node dysfunction	https://identifiers.org/kegg.disease:H00729
NANDO:2100051	http://nanbyodata.jp/ontology/NANDO_2100051	心房細動	Atrial fibrillation	H00731	http://www.geneontology.org/formats/oboInOwl#hasDbXref	心房細動	Atrial fibrillation	https://identifiers.org/kegg.disease:H00731
NANDO:2100053	http://nanbyodata.jp/ontology/NANDO_2100053	QT延長症候群	Long QT syndrome	H00720	http://www.geneontology.org/formats/oboInOwl#hasDbXref	QT 延長症候群	Long QT syndrome	https://identifiers.org/kegg.disease:H00720
NANDO:2100054	http://nanbyodata.jp/ontology/NANDO_2100054	肥大型心筋症	Hypertrophic cardiomyopathy	H00292	http://www.geneontology.org/formats/oboInOwl#hasDbXref	肥大型心筋症	Hypertrophic cardiomyopathy	https://identifiers.org/kegg.disease:H00292
NANDO:2100055	http://nanbyodata.jp/ontology/NANDO_2100055	不整脈源性右室心筋症	Arrhythmogenic right ventricular cardiomyopathy or dysplasia	H00293	http://www.geneontology.org/formats/oboInOwl#hasDbXref	不整脈源性右室心筋症	Arrhythmogenic right ventricular cardiomyopathy	https://identifiers.org/kegg.disease:H00293
NANDO:2100057	http://nanbyodata.jp/ontology/NANDO_2100057	拡張型心筋症	Dilated cardiomyopathy	H00294	http://www.geneontology.org/formats/oboInOwl#hasDbXref	拡張型心筋症	Dilated cardiomyopathy	https://identifiers.org/kegg.disease:H00294
NANDO:2100058	http://nanbyodata.jp/ontology/NANDO_2100058	拘束型心筋症	Restrictive cardiomyopathy	H01219	http://www.geneontology.org/formats/oboInOwl#hasDbXref	拘束性心筋症	Restrictive cardiomyopathy	https://identifiers.org/kegg.disease:H01219
NANDO:2100071	http://nanbyodata.jp/ontology/NANDO_2100071	左心低形成症候群	Hypoplastic left heart syndrome	H01272	http://www.geneontology.org/formats/oboInOwl#hasDbXref	左心低形成症候群	Hypoplastic left heart syndrome	https://identifiers.org/kegg.disease:H01272
NANDO:2100072	http://nanbyodata.jp/ontology/NANDO_2100072	単心室症	Single ventricle	H01787	http://www.geneontology.org/formats/oboInOwl#hasDbXref	単心室症	Univentricular heart	https://identifiers.org/kegg.disease:H01787
NANDO:2100073	http://nanbyodata.jp/ontology/NANDO_2100073	三尖弁閉鎖症	Tricuspid atresia	H01785	http://www.geneontology.org/formats/oboInOwl#hasDbXref	三尖弁閉鎖症	Tricuspid atresia	https://identifiers.org/kegg.disease:H01785
NANDO:2100075	http://nanbyodata.jp/ontology/NANDO_2100075	ファロー四徴症	Tetralogy of Fallot	H00549	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ファロー四徴症	Tetralogy of Fallot	https://identifiers.org/kegg.disease:H00549
NANDO:2100076	http://nanbyodata.jp/ontology/NANDO_2100076	両大血管右室起始症	Double outlet right ventricle	H00918	http://www.geneontology.org/formats/oboInOwl#hasDbXref	両大血管右室起始症	Double-outlet right ventricle	https://identifiers.org/kegg.disease:H00918
NANDO:2100078	http://nanbyodata.jp/ontology/NANDO_2100078	完全大血管転位症	Complete transposition of the great arteries	H00550	http://www.geneontology.org/formats/oboInOwl#hasDbXref	完全大血管転位症	Complete transposition of the great arteries	https://identifiers.org/kegg.disease:H00550
NANDO:2100080	http://nanbyodata.jp/ontology/NANDO_2100080	エプスタイン病	Ebstein's anomaly	H01783	http://www.geneontology.org/formats/oboInOwl#hasDbXref	エプスタイン病	Ebstein anomaly	https://identifiers.org/kegg.disease:H01783
NANDO:2100081	http://nanbyodata.jp/ontology/NANDO_2100081	総動脈幹遺残症	Truncus arteriosus communis	H01736	http://www.geneontology.org/formats/oboInOwl#hasDbXref	総動脈幹遺残症	Persistent truncus arteriosus	https://identifiers.org/kegg.disease:H01736
NANDO:2100084	http://nanbyodata.jp/ontology/NANDO_2100084	動脈管開存症	Patent ductus arteriosus	H01630	http://www.geneontology.org/formats/oboInOwl#hasDbXref	動脈管開存症	Patent ductus arteriosus	https://identifiers.org/kegg.disease:H01630
NANDO:2100085	http://nanbyodata.jp/ontology/NANDO_2100085	心房中隔欠損症	Atrial septal defect	H00546	http://www.geneontology.org/formats/oboInOwl#hasDbXref	心房中隔欠損	Atrial septal defect	https://identifiers.org/kegg.disease:H00546
NANDO:2100103	http://nanbyodata.jp/ontology/NANDO_2100103	肺動脈性肺高血圧症	Pulmonary arterial hypertension	H01621	http://www.geneontology.org/formats/oboInOwl#hasDbXref	肺動脈性肺高血圧症	Pulmonary arterial hypertension	https://identifiers.org/kegg.disease:H01621
NANDO:2100111	http://nanbyodata.jp/ontology/NANDO_2100111	下垂体性巨人症	Pituitary gigantism	H01618	http://www.geneontology.org/formats/oboInOwl#hasDbXref	下垂体性巨人症	Pituitary gigantism	https://identifiers.org/kegg.disease:H01618
NANDO:2100112	http://nanbyodata.jp/ontology/NANDO_2100112	先端巨大症	Acromegaly	H01483	http://www.geneontology.org/formats/oboInOwl#hasDbXref	先端巨大症	Acromegaly	https://identifiers.org/kegg.disease:H01483
NANDO:2100115	http://nanbyodata.jp/ontology/NANDO_2100115	高プロラクチン血症	Hyperprolactinemia	H01388	http://www.geneontology.org/formats/oboInOwl#hasDbXref	高プロラクチン血症	Hyperprolactinemia	https://identifiers.org/kegg.disease:H01388
NANDO:2100115	http://nanbyodata.jp/ontology/NANDO_2100115	高プロラクチン血症	Hyperprolactinemia	H01388	http://www.geneontology.org/formats/oboInOwl#hasDbXref	下垂体性 PRL 分泌亢進症	Hyperprolactinemia	https://identifiers.org/kegg.disease:H01388
NANDO:2100119	http://nanbyodata.jp/ontology/NANDO_2100119	甲状腺機能亢進症	Hyperthyroidism	H01645	http://www.geneontology.org/formats/oboInOwl#hasDbXref	甲状腺機能亢進症	Hyperthyroidism	https://identifiers.org/kegg.disease:H01645
NANDO:2100119	http://nanbyodata.jp/ontology/NANDO_2100119	甲状腺機能亢進症	Hyperthyroidism	H01645	http://www.geneontology.org/formats/oboInOwl#hasDbXref	甲状腺中毒症	Hyperthyroidism	https://identifiers.org/kegg.disease:H01645
NANDO:2100119	http://nanbyodata.jp/ontology/NANDO_2100119	甲状腺機能亢進症	Hyperthyroidism	H01645	http://www.geneontology.org/formats/oboInOwl#hasDbXref	甲状腺機能亢進症	Thyrotoxicosis	https://identifiers.org/kegg.disease:H01645
NANDO:2100119	http://nanbyodata.jp/ontology/NANDO_2100119	甲状腺機能亢進症	Hyperthyroidism	H01645	http://www.geneontology.org/formats/oboInOwl#hasDbXref	甲状腺中毒症	Thyrotoxicosis	https://identifiers.org/kegg.disease:H01645
NANDO:2100123	http://nanbyodata.jp/ontology/NANDO_2100123	副甲状腺機能亢進症	Hyperparathyroidism	H00246	http://www.geneontology.org/formats/oboInOwl#hasDbXref	副甲状腺機能亢進症	Familial hyperparathyroidism	https://identifiers.org/kegg.disease:H00246
NANDO:2100123	http://nanbyodata.jp/ontology/NANDO_2100123	副甲状腺機能亢進症	Hyperparathyroidism	H00246	http://www.geneontology.org/formats/oboInOwl#hasDbXref	副甲状腺機能亢進症	Primary hyperparathyroidism	https://identifiers.org/kegg.disease:H00246
NANDO:2100124	http://nanbyodata.jp/ontology/NANDO_2100124	副甲状腺機能低下症	Hypoparathyroidism	H01862	http://www.geneontology.org/formats/oboInOwl#hasDbXref	副甲状腺機能低下症	Hypoparathyroidism	https://identifiers.org/kegg.disease:H01862
NANDO:2100126	http://nanbyodata.jp/ontology/NANDO_2100126	偽性副甲状腺機能低下症	Pseudohypoparathyroidism	H00244	http://www.geneontology.org/formats/oboInOwl#hasDbXref	偽性副甲状腺機能低下症	Pseudohypoparathyroidism	https://identifiers.org/kegg.disease:H00244
NANDO:2100127	http://nanbyodata.jp/ontology/NANDO_2100127	クッシング症候群	Cushing (Cushing) syndrome	H01431	http://www.geneontology.org/formats/oboInOwl#hasDbXref	クッシング症候群	Cushing syndrome	https://identifiers.org/kegg.disease:H01431
NANDO:2100130	http://nanbyodata.jp/ontology/NANDO_2100130	見かけの鉱質コルチコイド過剰症候群	Apparent mineralocorticoid excess syndrome	H00259	http://www.geneontology.org/formats/oboInOwl#hasDbXref	AME 症候群	Apparent mineralocorticoid excess syndrome	https://identifiers.org/kegg.disease:H00259
NANDO:2100130	http://nanbyodata.jp/ontology/NANDO_2100130	見かけの鉱質コルチコイド過剰症候群	Apparent mineralocorticoid excess syndrome	H00259	http://www.geneontology.org/formats/oboInOwl#hasDbXref	11β-ヒドロキシステロイドデヒドロゲナーゼ欠損症	Apparent mineralocorticoid excess syndrome	https://identifiers.org/kegg.disease:H00259
NANDO:2100130	http://nanbyodata.jp/ontology/NANDO_2100130	見かけの鉱質コルチコイド過剰症候群	Apparent mineralocorticoid excess syndrome	H00259	http://www.geneontology.org/formats/oboInOwl#hasDbXref	AME 症候群	11-beta-ketoreductase deficiency	https://identifiers.org/kegg.disease:H00259
NANDO:2100130	http://nanbyodata.jp/ontology/NANDO_2100130	見かけの鉱質コルチコイド過剰症候群	Apparent mineralocorticoid excess syndrome	H00259	http://www.geneontology.org/formats/oboInOwl#hasDbXref	11β-ヒドロキシステロイドデヒドロゲナーゼ欠損症	11-beta-ketoreductase deficiency	https://identifiers.org/kegg.disease:H00259
NANDO:2100131	http://nanbyodata.jp/ontology/NANDO_2100131	リドル症候群	Liddle syndrome	H00242	http://www.geneontology.org/formats/oboInOwl#hasDbXref	リドル症候群	Liddle syndrome	https://identifiers.org/kegg.disease:H00242
NANDO:2100134	http://nanbyodata.jp/ontology/NANDO_2100134	先天性副腎過形成症	Congenital adrenal hyperplasia	H00216	http://www.geneontology.org/formats/oboInOwl#hasDbXref	先天性副腎過形成症	Congenital adrenal hyperplasia	https://identifiers.org/kegg.disease:H00216
NANDO:2100134	http://nanbyodata.jp/ontology/NANDO_2100134	先天性副腎過形成症	Congenital adrenal hyperplasia	H00216	http://www.geneontology.org/formats/oboInOwl#hasDbXref	先天性副腎酵素欠損症	Congenital adrenal hyperplasia	https://identifiers.org/kegg.disease:H00216
NANDO:2100135	http://nanbyodata.jp/ontology/NANDO_2100135	思春期早発症	Precocious puberty	H00937	http://www.geneontology.org/formats/oboInOwl#hasDbXref	思春期早発症	Precocious puberty	https://identifiers.org/kegg.disease:H00937
NANDO:2100138	http://nanbyodata.jp/ontology/NANDO_2100138	低ゴナドトロピン性性腺機能低下症	Hypogonadotropic hypogonadism	H00255	http://www.geneontology.org/formats/oboInOwl#hasDbXref	低ゴナドトロピン性性腺機能低下症	Hypogonadotropic hypogonadism	https://identifiers.org/kegg.disease:H00255
NANDO:2100144	http://nanbyodata.jp/ontology/NANDO_2100144	ビタミンD依存性くる病	Vitamin D-dependent rickets	H01143	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ビタミンD依存性くる病	Vitamin D-dependent rickets	https://identifiers.org/kegg.disease:H01143
NANDO:2100147	http://nanbyodata.jp/ontology/NANDO_2100147	脂肪萎縮症	Lipodystrophy	H01475	http://www.geneontology.org/formats/oboInOwl#hasDbXref	脂肪異栄養症	Lipodystrophy	https://identifiers.org/kegg.disease:H01475
NANDO:2100147	http://nanbyodata.jp/ontology/NANDO_2100147	脂肪萎縮症	Lipodystrophy	H01475	http://www.geneontology.org/formats/oboInOwl#hasDbXref	脂肪萎縮症	Lipodystrophy	https://identifiers.org/kegg.disease:H01475
NANDO:2100147	http://nanbyodata.jp/ontology/NANDO_2100147	脂肪萎縮症	Lipodystrophy	H01475	http://www.geneontology.org/formats/oboInOwl#hasDbXref	リポジストロフィー	Lipodystrophy	https://identifiers.org/kegg.disease:H01475
NANDO:2100147	http://nanbyodata.jp/ontology/NANDO_2100147	脂肪萎縮症	Lipodystrophy	H01475	http://www.geneontology.org/formats/oboInOwl#hasDbXref	脂肪異栄養症	Lipoatrophy	https://identifiers.org/kegg.disease:H01475
NANDO:2100147	http://nanbyodata.jp/ontology/NANDO_2100147	脂肪萎縮症	Lipodystrophy	H01475	http://www.geneontology.org/formats/oboInOwl#hasDbXref	脂肪萎縮症	Lipoatrophy	https://identifiers.org/kegg.disease:H01475
NANDO:2100147	http://nanbyodata.jp/ontology/NANDO_2100147	脂肪萎縮症	Lipodystrophy	H01475	http://www.geneontology.org/formats/oboInOwl#hasDbXref	リポジストロフィー	Lipoatrophy	https://identifiers.org/kegg.disease:H01475
NANDO:2100149	http://nanbyodata.jp/ontology/NANDO_2100149	多嚢胞性卵巣症候群	Polycystic ovary syndrome	H01739	http://www.geneontology.org/formats/oboInOwl#hasDbXref	多嚢胞性卵巣症候群	Polycystic ovary syndrome	https://identifiers.org/kegg.disease:H01739
NANDO:2100154	http://nanbyodata.jp/ontology/NANDO_2100154	再発性多発軟骨炎	Relapsing Polychondritis	H01758	http://www.geneontology.org/formats/oboInOwl#hasDbXref	再発性多発軟骨炎	Relapsing polychondritis	https://identifiers.org/kegg.disease:H01758
NANDO:2100163	http://nanbyodata.jp/ontology/NANDO_2100163	ミトコンドリア病	Mitochondrial diseases	H01427	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ミトコンドリア病	Mitochondrial disease	https://identifiers.org/kegg.disease:H01427
NANDO:2100165	http://nanbyodata.jp/ontology/NANDO_2100165	ライソゾーム病	Lysosomal storage disease	H01425	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ライソゾーム病 (リソソーム蓄積症)	Lysosomal storage disease	https://identifiers.org/kegg.disease:H01425
NANDO:2100174	http://nanbyodata.jp/ontology/NANDO_2100174	α1-アンチトリプシン欠損症	Alpha-1-antitrypsin deficiency	H01103	http://www.geneontology.org/formats/oboInOwl#hasDbXref	α1-アンチトリプシン欠乏症	Alpha-1-antitrypsin deficiency	https://identifiers.org/kegg.disease:H01103
NANDO:2100178	http://nanbyodata.jp/ontology/NANDO_2100178	先天性赤血球形成異常性貧血	Congenital dyserythropoietic anemia	H00917	http://www.geneontology.org/formats/oboInOwl#hasDbXref	先天性赤血球形成異常性貧血	Congenital dyserythropoietic anemia	https://identifiers.org/kegg.disease:H00917
NANDO:2100178	http://nanbyodata.jp/ontology/NANDO_2100178	先天性赤血球形成異常性貧血	Congenital dyserythropoietic anemia	H00917	http://www.geneontology.org/formats/oboInOwl#hasDbXref	先天性赤血球生成不全性貧血	Congenital dyserythropoietic anemia	https://identifiers.org/kegg.disease:H00917
NANDO:2100178	http://nanbyodata.jp/ontology/NANDO_2100178	先天性赤血球形成異常性貧血	Congenital dyserythropoietic anemia	H00917	http://www.geneontology.org/formats/oboInOwl#hasDbXref	先天性赤血球異形成貧血	Congenital dyserythropoietic anemia	https://identifiers.org/kegg.disease:H00917
NANDO:2100180	http://nanbyodata.jp/ontology/NANDO_2100180	無トランスフェリン血症	Congenital atransferrinemia	H01145	http://www.geneontology.org/formats/oboInOwl#hasDbXref	無トランスフェリン血症	Congenital hypotransferrinemia	https://identifiers.org/kegg.disease:H01145
NANDO:2100180	http://nanbyodata.jp/ontology/NANDO_2100180	無トランスフェリン血症	Congenital atransferrinemia	H01145	http://www.geneontology.org/formats/oboInOwl#hasDbXref	無トランスフェリン血症	Atransferrinemia	https://identifiers.org/kegg.disease:H01145
NANDO:2100181	http://nanbyodata.jp/ontology/NANDO_2100181	自己免疫性溶血性貧血	Autoimmune hemolytic anemia	H01585	http://www.geneontology.org/formats/oboInOwl#hasDbXref	自己免疫性溶血性貧血	Autoimmune hemolytic anemia	https://identifiers.org/kegg.disease:H01585
NANDO:2100182	http://nanbyodata.jp/ontology/NANDO_2100182	発作性夜間ヘモグロビン尿症	Paroxysmal nocturnal haemoglobinuria	H01053	http://www.geneontology.org/formats/oboInOwl#hasDbXref	発作性夜間ヘモグロビン尿症	Paroxysmal nocturnal hemoglobinuria	https://identifiers.org/kegg.disease:H01053
NANDO:2100187	http://nanbyodata.jp/ontology/NANDO_2100187	家族性赤血球増加症	Familial polycythemia	H00236	http://www.geneontology.org/formats/oboInOwl#hasDbXref	家族性赤血球増加症	Congenital polycythemia	https://identifiers.org/kegg.disease:H00236
NANDO:2100187	http://nanbyodata.jp/ontology/NANDO_2100187	家族性赤血球増加症	Familial polycythemia	H00236	http://www.geneontology.org/formats/oboInOwl#hasDbXref	先天性赤血球増加症	Congenital polycythemia	https://identifiers.org/kegg.disease:H00236
NANDO:2100187	http://nanbyodata.jp/ontology/NANDO_2100187	家族性赤血球増加症	Familial polycythemia	H00236	http://www.geneontology.org/formats/oboInOwl#hasDbXref	家族性赤血球増加症	Familial erythrocytosis (ECYT)	https://identifiers.org/kegg.disease:H00236
NANDO:2100187	http://nanbyodata.jp/ontology/NANDO_2100187	家族性赤血球増加症	Familial polycythemia	H00236	http://www.geneontology.org/formats/oboInOwl#hasDbXref	先天性赤血球増加症	Familial erythrocytosis (ECYT)	https://identifiers.org/kegg.disease:H00236
NANDO:2100189	http://nanbyodata.jp/ontology/NANDO_2100189	血栓性血小板減少性紫斑病	Thrombotic thrombocytopenic purpura	H00225	http://www.geneontology.org/formats/oboInOwl#hasDbXref	血栓性血小板減少性紫斑病	Thrombotic thrombocytopenic purpura	https://identifiers.org/kegg.disease:H00225
NANDO:2100189	http://nanbyodata.jp/ontology/NANDO_2100189	血栓性血小板減少性紫斑病	Thrombotic thrombocytopenic purpura	H00225	http://www.geneontology.org/formats/oboInOwl#hasDbXref	血栓性血小板減少性紫斑病	Moschcowitz disease	https://identifiers.org/kegg.disease:H00225
NANDO:2100189	http://nanbyodata.jp/ontology/NANDO_2100189	血栓性血小板減少性紫斑病	Thrombotic thrombocytopenic purpura	H00225	http://www.geneontology.org/formats/oboInOwl#hasDbXref	血栓性血小板減少性紫斑病	Schulman-Upshaw syndrome	https://identifiers.org/kegg.disease:H00225
NANDO:2100194	http://nanbyodata.jp/ontology/NANDO_2100194	本態性血小板血症	Essential thrombocythemia	H01612	http://www.geneontology.org/formats/oboInOwl#hasDbXref	本態性血小板血症	Essential thrombocythemia	https://identifiers.org/kegg.disease:H01612
NANDO:2100194	http://nanbyodata.jp/ontology/NANDO_2100194	本態性血小板血症	Essential thrombocythemia	H01612	http://www.geneontology.org/formats/oboInOwl#hasDbXref	本態性血小板血症	Essential thrombocytosis	https://identifiers.org/kegg.disease:H01612
NANDO:2100194	http://nanbyodata.jp/ontology/NANDO_2100194	本態性血小板血症	Essential thrombocythemia	H01612	http://www.geneontology.org/formats/oboInOwl#hasDbXref	本態性血小板血症	Thrombocythemia	https://identifiers.org/kegg.disease:H01612
NANDO:2100200	http://nanbyodata.jp/ontology/NANDO_2100200	骨髄線維症	Myelofibrosis	H01605	http://www.geneontology.org/formats/oboInOwl#hasDbXref	骨髄線維症	Myelofibrosis	https://identifiers.org/kegg.disease:H01605
NANDO:2100201	http://nanbyodata.jp/ontology/NANDO_2100201	再生不良性貧血	Aplastic anemia	H01132	http://www.geneontology.org/formats/oboInOwl#hasDbXref	再生不良性貧血	Aplastic anemia	https://identifiers.org/kegg.disease:H01132
NANDO:2100203	http://nanbyodata.jp/ontology/NANDO_2100203	複合免疫不全症	Combined immunodeficiency	H00093	http://www.geneontology.org/formats/oboInOwl#hasDbXref	複合免疫不全症	Combined immunodeficiency	https://identifiers.org/kegg.disease:H00093
NANDO:2100218	http://nanbyodata.jp/ontology/NANDO_2100218	ジュベール症候群関連疾患	Joubert syndrome related disorders	H00530	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ジュベール症候群関連疾患	Joubert syndrome and related disorders	https://identifiers.org/kegg.disease:H00530
NANDO:2100219	http://nanbyodata.jp/ontology/NANDO_2100219	レット症候群	Rett syndrome	H00440	http://www.geneontology.org/formats/oboInOwl#hasDbXref	レット症候群	Rett syndrome	https://identifiers.org/kegg.disease:H00440
NANDO:2100223	http://nanbyodata.jp/ontology/NANDO_2100223	ATR-X症候群	ATR-X syndrome	H01752	http://www.geneontology.org/formats/oboInOwl#hasDbXref	X連鎖アルファサラセミア精神遅滞症候群	ATR-X syndrome	https://identifiers.org/kegg.disease:H01752
NANDO:2100223	http://nanbyodata.jp/ontology/NANDO_2100223	ATR-X症候群	ATR-X syndrome	H01752	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ATR-X 症候群	ATR-X syndrome	https://identifiers.org/kegg.disease:H01752
NANDO:2100223	http://nanbyodata.jp/ontology/NANDO_2100223	ATR-X症候群	ATR-X syndrome	H01752	http://www.geneontology.org/formats/oboInOwl#hasDbXref	X連鎖アルファサラセミア精神遅滞症候群	X-linked alpha-thalassemia/mental retardation syndrome	https://identifiers.org/kegg.disease:H01752
NANDO:2100223	http://nanbyodata.jp/ontology/NANDO_2100223	ATR-X症候群	ATR-X syndrome	H01752	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ATR-X 症候群	X-linked alpha-thalassemia/mental retardation syndrome	https://identifiers.org/kegg.disease:H01752
NANDO:2100224	http://nanbyodata.jp/ontology/NANDO_2100224	脆弱Ｘ症候群	Fragile X syndrome	H00465	http://www.geneontology.org/formats/oboInOwl#hasDbXref	脆弱Ｘ症候群	Fragile X syndrome	https://identifiers.org/kegg.disease:H00465
NANDO:2100226	http://nanbyodata.jp/ontology/NANDO_2100226	脳クレアチン欠乏症候群	Cerebral creatine deficiency syndromes	H00849	http://www.geneontology.org/formats/oboInOwl#hasDbXref	脳クレアチン欠乏症候群	Cerebral creatine deficiency syndrome	https://identifiers.org/kegg.disease:H00849
NANDO:2100228	http://nanbyodata.jp/ontology/NANDO_2100228	もやもや病	Moyamoya disease	H01396	http://www.geneontology.org/formats/oboInOwl#hasDbXref	もやもや病	Moyamoya disease	https://identifiers.org/kegg.disease:H01396
NANDO:2100231	http://nanbyodata.jp/ontology/NANDO_2100231	脊髄性筋萎縮症	Spinal muscular atrophy	H00455	http://www.geneontology.org/formats/oboInOwl#hasDbXref	脊髄性筋萎縮症	Spinal muscular atrophy	https://identifiers.org/kegg.disease:H00455
NANDO:2100234	http://nanbyodata.jp/ontology/NANDO_2100234	先天性ミオパチー	Congenital myopathy	H01810	http://www.geneontology.org/formats/oboInOwl#hasDbXref	先天性ミオパチー	Congenital myopathy	https://identifiers.org/kegg.disease:H01810
NANDO:2100235	http://nanbyodata.jp/ontology/NANDO_2100235	シュワルツ・ヤンペル症候群	Schwartz-Jampel syndrome	H01777	http://www.geneontology.org/formats/oboInOwl#hasDbXref	シュワルツ・ヤンペル症候群	Schwartz-Jampel syndrome	https://identifiers.org/kegg.disease:H01777
NANDO:2100237	http://nanbyodata.jp/ontology/NANDO_2100237	進行性ミオクローヌスてんかん	Progressive myoclonus epilepsy	H00810	http://www.geneontology.org/formats/oboInOwl#hasDbXref	進行性ミオクローヌスてんかん	Progressive myoclonic epilepsy	https://identifiers.org/kegg.disease:H00810
NANDO:2100238	http://nanbyodata.jp/ontology/NANDO_2100238	脊髄小脳変性症	Spinocerebellar degeneration	H01616	http://www.geneontology.org/formats/oboInOwl#hasDbXref	脊髄小脳変性症	Spinocerebellar degeneration	https://identifiers.org/kegg.disease:H01616
NANDO:2100239	http://nanbyodata.jp/ontology/NANDO_2100239	小児交互性片麻痺	Alternating hemiplegia of childhood	H00998	http://www.geneontology.org/formats/oboInOwl#hasDbXref	小児交互性片麻痺	Alternating hemiplegia of childhood	https://identifiers.org/kegg.disease:H00998
NANDO:2100241	http://nanbyodata.jp/ontology/NANDO_2100241	脳の鉄沈着を伴う神経変性疾患	Neurodegeneration with brain iron accumulation	H00833	http://www.geneontology.org/formats/oboInOwl#hasDbXref	脳の鉄沈着を伴う神経変性疾患	Neurodegeneration with brain iron accumulation	https://identifiers.org/kegg.disease:H00833
NANDO:2100242	http://nanbyodata.jp/ontology/NANDO_2100242	乳児両側線条体壊死	Infantile bilateral striatal necrosis	H01177	http://www.geneontology.org/formats/oboInOwl#hasDbXref	乳児両側性線条体壊死	Infantile bilateral striatal necrosis	https://identifiers.org/kegg.disease:H01177
NANDO:2100244	http://nanbyodata.jp/ontology/NANDO_2100244	エカルディ・グティエール症候群	Aicardi-Goutières Syndrome	H00290	http://www.geneontology.org/formats/oboInOwl#hasDbXref	エカルディ・グティエール症候群	Aicardi-Goutieres syndrome	https://identifiers.org/kegg.disease:H00290
NANDO:2100245	http://nanbyodata.jp/ontology/NANDO_2100245	亜急性硬化性全脳炎	Subacute sclerosing panencephalitis	H01696	http://www.geneontology.org/formats/oboInOwl#hasDbXref	亜急性硬化性全脳炎	Subacute sclerosing panencephalitis	https://identifiers.org/kegg.disease:H01696
NANDO:2100246	http://nanbyodata.jp/ontology/NANDO_2100246	ラスムッセン脳炎	Rasmussen's encephalitis	H01812	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ラスムッセン脳炎	Rasmussen encephalitis	https://identifiers.org/kegg.disease:H01812
NANDO:2100246	http://nanbyodata.jp/ontology/NANDO_2100246	ラスムッセン脳炎	Rasmussen's encephalitis	H01812	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ラスムッセン症候群	Rasmussen encephalitis	https://identifiers.org/kegg.disease:H01812
NANDO:2100246	http://nanbyodata.jp/ontology/NANDO_2100246	ラスムッセン脳炎	Rasmussen's encephalitis	H01812	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ラスムッセン脳炎	Rasmussen syndrome	https://identifiers.org/kegg.disease:H01812
NANDO:2100246	http://nanbyodata.jp/ontology/NANDO_2100246	ラスムッセン脳炎	Rasmussen's encephalitis	H01812	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ラスムッセン症候群	Rasmussen syndrome	https://identifiers.org/kegg.disease:H01812
NANDO:2100247	http://nanbyodata.jp/ontology/NANDO_2100247	痙攣重積型急性脳症	Acute encephalopathy with biphasic seizures and late reduced diffusion	H01841	http://www.geneontology.org/formats/oboInOwl#hasDbXref	痙攣重積型 (二相性) 急性脳症	Acute encephalopathy with biphasic seizures and late reduced diffusion	https://identifiers.org/kegg.disease:H01841
NANDO:2100249	http://nanbyodata.jp/ontology/NANDO_2100249	難治頻回部分発作重積型急性脳炎	Acute encephalitis with refractory, repetitive partial seizures	H01829	http://www.geneontology.org/formats/oboInOwl#hasDbXref	難治頻回部分発作重積型急性脳炎	Acute encephalitis with refractory repetitive partial seizures	https://identifiers.org/kegg.disease:H01829
NANDO:2100250	http://nanbyodata.jp/ontology/NANDO_2100250	多発性硬化症	Multiple sclerosis	H01490	http://www.geneontology.org/formats/oboInOwl#hasDbXref	多発性硬化症	Multiple sclerosis	https://identifiers.org/kegg.disease:H01490
NANDO:2100251	http://nanbyodata.jp/ontology/NANDO_2100251	慢性炎症性脱髄性多発神経炎	Chronic inflammatory demyelinating polyneuropathy	H01527	http://www.geneontology.org/formats/oboInOwl#hasDbXref	多巣性運動ニューロパチー	Chronic inflammatory demyelinating polyradiculoneuropathy	https://identifiers.org/kegg.disease:H01527
NANDO:2100251	http://nanbyodata.jp/ontology/NANDO_2100251	慢性炎症性脱髄性多発神経炎	Chronic inflammatory demyelinating polyneuropathy	H01527	http://www.geneontology.org/formats/oboInOwl#hasDbXref	慢性炎症性脱髄性多発神経炎	Chronic inflammatory demyelinating polyradiculoneuropathy	https://identifiers.org/kegg.disease:H01527
NANDO:2100252	http://nanbyodata.jp/ontology/NANDO_2100252	重症筋無力症	Myasthenia gravis	H01594	http://www.geneontology.org/formats/oboInOwl#hasDbXref	重症筋無力症	Myasthenia gravis	https://identifiers.org/kegg.disease:H01594
NANDO:2100261	http://nanbyodata.jp/ontology/NANDO_2100261	非特異性多発性小腸潰瘍症	Chronic nonspecific multiple ulcers of the small intestine	H01853	http://www.geneontology.org/formats/oboInOwl#hasDbXref	非特異性多発性小腸潰瘍症	Chronic nonspecific multiple ulcers of the small intestine	https://identifiers.org/kegg.disease:H01853
NANDO:2100283	http://nanbyodata.jp/ontology/NANDO_2100283	先天性魚鱗癬	Congenital ichthyosis	H01771	http://www.geneontology.org/formats/oboInOwl#hasDbXref	先天性魚鱗癬	Congenital ichthyosis	https://identifiers.org/kegg.disease:H01771
NANDO:2100284	http://nanbyodata.jp/ontology/NANDO_2100284	表皮水疱症	Epidermolysis bullosa	H01737	http://www.geneontology.org/formats/oboInOwl#hasDbXref	表皮水疱症	Epidermolysis bullosa	https://identifiers.org/kegg.disease:H01737
NANDO:2100285	http://nanbyodata.jp/ontology/NANDO_2100285	膿疱性乾癬（汎発型）	Pustular psoriasis	H01663	http://www.geneontology.org/formats/oboInOwl#hasDbXref	膿疱性乾癬	Pustular psoriasis	https://identifiers.org/kegg.disease:H01663
NANDO:2100286	http://nanbyodata.jp/ontology/NANDO_2100286	色素性乾皮症	Xeroderma pigmentosum	H01428	http://www.geneontology.org/formats/oboInOwl#hasDbXref	色素性乾皮症	Xeroderma pigmentosum	https://identifiers.org/kegg.disease:H01428
NANDO:2100287	http://nanbyodata.jp/ontology/NANDO_2100287	レックリングハウゼン病	von Recklinghausen's disease	H01437	http://www.geneontology.org/formats/oboInOwl#hasDbXref	レックリングハウゼン病	Neurofibromatosis type 1	https://identifiers.org/kegg.disease:H01437
NANDO:2100287	http://nanbyodata.jp/ontology/NANDO_2100287	レックリングハウゼン病	von Recklinghausen's disease	H01437	http://www.geneontology.org/formats/oboInOwl#hasDbXref	神経線維腫症 I 型	Neurofibromatosis type 1	https://identifiers.org/kegg.disease:H01437
NANDO:2100287	http://nanbyodata.jp/ontology/NANDO_2100287	レックリングハウゼン病	von Recklinghausen's disease	H01437	http://www.geneontology.org/formats/oboInOwl#hasDbXref	レックリングハウゼン病	Von Recklinghausen disease	https://identifiers.org/kegg.disease:H01437
NANDO:2100287	http://nanbyodata.jp/ontology/NANDO_2100287	レックリングハウゼン病	von Recklinghausen's disease	H01437	http://www.geneontology.org/formats/oboInOwl#hasDbXref	神経線維腫症 I 型	Von Recklinghausen disease	https://identifiers.org/kegg.disease:H01437
NANDO:2100290	http://nanbyodata.jp/ontology/NANDO_2100290	スティーヴンス・ジョンソン症候群	Stevens-Johnson syndrome	H01694	http://www.geneontology.org/formats/oboInOwl#hasDbXref	中毒性表皮壊死症	Stevens-Johnson syndrome	https://identifiers.org/kegg.disease:H01694
NANDO:2100290	http://nanbyodata.jp/ontology/NANDO_2100290	スティーヴンス・ジョンソン症候群	Stevens-Johnson syndrome	H01694	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ライエル症候群	Stevens-Johnson syndrome	https://identifiers.org/kegg.disease:H01694
NANDO:2100290	http://nanbyodata.jp/ontology/NANDO_2100290	スティーヴンス・ジョンソン症候群	Stevens-Johnson syndrome	H01694	http://www.geneontology.org/formats/oboInOwl#hasDbXref	スティーブンス・ジョンソン症候群	Stevens-Johnson syndrome	https://identifiers.org/kegg.disease:H01694
NANDO:2100290	http://nanbyodata.jp/ontology/NANDO_2100290	スティーヴンス・ジョンソン症候群	Stevens-Johnson syndrome	H01694	http://www.geneontology.org/formats/oboInOwl#hasDbXref	重症多形滲出性紅斑	Stevens-Johnson syndrome	https://identifiers.org/kegg.disease:H01694
NANDO:2100290	http://nanbyodata.jp/ontology/NANDO_2100290	スティーヴンス・ジョンソン症候群	Stevens-Johnson syndrome	H01694	http://www.geneontology.org/formats/oboInOwl#hasDbXref	中毒性表皮壊死症	Toxic epidermal necrolysis	https://identifiers.org/kegg.disease:H01694
NANDO:2100290	http://nanbyodata.jp/ontology/NANDO_2100290	スティーヴンス・ジョンソン症候群	Stevens-Johnson syndrome	H01694	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ライエル症候群	Toxic epidermal necrolysis	https://identifiers.org/kegg.disease:H01694
NANDO:2100290	http://nanbyodata.jp/ontology/NANDO_2100290	スティーヴンス・ジョンソン症候群	Stevens-Johnson syndrome	H01694	http://www.geneontology.org/formats/oboInOwl#hasDbXref	スティーブンス・ジョンソン症候群	Toxic epidermal necrolysis	https://identifiers.org/kegg.disease:H01694
NANDO:2100290	http://nanbyodata.jp/ontology/NANDO_2100290	スティーヴンス・ジョンソン症候群	Stevens-Johnson syndrome	H01694	http://www.geneontology.org/formats/oboInOwl#hasDbXref	重症多形滲出性紅斑	Toxic epidermal necrolysis	https://identifiers.org/kegg.disease:H01694
NANDO:2100290	http://nanbyodata.jp/ontology/NANDO_2100290	スティーヴンス・ジョンソン症候群	Stevens-Johnson syndrome	H01694	http://www.geneontology.org/formats/oboInOwl#hasDbXref	中毒性表皮壊死症	Lyell syndrome	https://identifiers.org/kegg.disease:H01694
NANDO:2100290	http://nanbyodata.jp/ontology/NANDO_2100290	スティーヴンス・ジョンソン症候群	Stevens-Johnson syndrome	H01694	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ライエル症候群	Lyell syndrome	https://identifiers.org/kegg.disease:H01694
NANDO:2100290	http://nanbyodata.jp/ontology/NANDO_2100290	スティーヴンス・ジョンソン症候群	Stevens-Johnson syndrome	H01694	http://www.geneontology.org/formats/oboInOwl#hasDbXref	スティーブンス・ジョンソン症候群	Lyell syndrome	https://identifiers.org/kegg.disease:H01694
NANDO:2100290	http://nanbyodata.jp/ontology/NANDO_2100290	スティーヴンス・ジョンソン症候群	Stevens-Johnson syndrome	H01694	http://www.geneontology.org/formats/oboInOwl#hasDbXref	重症多形滲出性紅斑	Lyell syndrome	https://identifiers.org/kegg.disease:H01694
NANDO:2100296	http://nanbyodata.jp/ontology/NANDO_2100296	遺伝性出血性末梢血管拡張症	Hereditary hemorrhagic telangiectasia	H00533	http://www.geneontology.org/formats/oboInOwl#hasDbXref	オスラー病	Hereditary hemorrhagic telangiectasia	https://identifiers.org/kegg.disease:H00533
NANDO:2100296	http://nanbyodata.jp/ontology/NANDO_2100296	遺伝性出血性末梢血管拡張症	Hereditary hemorrhagic telangiectasia	H00533	http://www.geneontology.org/formats/oboInOwl#hasDbXref	遺伝性出血性毛細血管拡張症	Hereditary hemorrhagic telangiectasia	https://identifiers.org/kegg.disease:H00533
NANDO:2100296	http://nanbyodata.jp/ontology/NANDO_2100296	遺伝性出血性末梢血管拡張症	Hereditary hemorrhagic telangiectasia	H00533	http://www.geneontology.org/formats/oboInOwl#hasDbXref	オスラー病	Osler disease	https://identifiers.org/kegg.disease:H00533
NANDO:2100296	http://nanbyodata.jp/ontology/NANDO_2100296	遺伝性出血性末梢血管拡張症	Hereditary hemorrhagic telangiectasia	H00533	http://www.geneontology.org/formats/oboInOwl#hasDbXref	遺伝性出血性毛細血管拡張症	Osler disease	https://identifiers.org/kegg.disease:H00533
NANDO:2100299	http://nanbyodata.jp/ontology/NANDO_2100299	ホルト・オーラム症候群	Holt-Oram syndrome	H00433	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ホルト・オラム症候群	Holt-Oram syndrome	https://identifiers.org/kegg.disease:H00433
NANDO:2100304	http://nanbyodata.jp/ontology/NANDO_2100304	限局性強皮症	Localized scleroderma/morphea	H01493	http://www.geneontology.org/formats/oboInOwl#hasDbXref	限局性強皮症	Localized Scleroderma	https://identifiers.org/kegg.disease:H01493
NANDO:2100304	http://nanbyodata.jp/ontology/NANDO_2100304	限局性強皮症	Localized scleroderma/morphea	H01493	http://www.geneontology.org/formats/oboInOwl#hasDbXref	モルフィア	Localized Scleroderma	https://identifiers.org/kegg.disease:H01493
NANDO:2100304	http://nanbyodata.jp/ontology/NANDO_2100304	限局性強皮症	Localized scleroderma/morphea	H01493	http://www.geneontology.org/formats/oboInOwl#hasDbXref	限局性強皮症	Morphea	https://identifiers.org/kegg.disease:H01493
NANDO:2100304	http://nanbyodata.jp/ontology/NANDO_2100304	限局性強皮症	Localized scleroderma/morphea	H01493	http://www.geneontology.org/formats/oboInOwl#hasDbXref	モルフィア	Morphea	https://identifiers.org/kegg.disease:H01493
NANDO:2200003	http://nanbyodata.jp/ontology/NANDO_2200003	T細胞急性リンパ性白血病	T-cell lymphoblastic leukemia	H00002	http://www.geneontology.org/formats/oboInOwl#hasDbXref	T細胞急性リンパ性白血病	T-cell acute lymphoblastic leukemia	https://identifiers.org/kegg.disease:H00002
NANDO:2200003	http://nanbyodata.jp/ontology/NANDO_2200003	T細胞急性リンパ性白血病	T-cell lymphoblastic leukemia	H00002	http://www.geneontology.org/formats/oboInOwl#hasDbXref	T細胞リンパ芽球性白血病	T-cell acute lymphoblastic leukemia	https://identifiers.org/kegg.disease:H00002
NANDO:2200003	http://nanbyodata.jp/ontology/NANDO_2200003	T細胞急性リンパ性白血病	T-cell lymphoblastic leukemia	H00002	http://www.geneontology.org/formats/oboInOwl#hasDbXref	T細胞急性リンパ性白血病	T-cell acute lymphocytic leukemia	https://identifiers.org/kegg.disease:H00002
NANDO:2200003	http://nanbyodata.jp/ontology/NANDO_2200003	T細胞急性リンパ性白血病	T-cell lymphoblastic leukemia	H00002	http://www.geneontology.org/formats/oboInOwl#hasDbXref	T細胞リンパ芽球性白血病	T-cell acute lymphocytic leukemia	https://identifiers.org/kegg.disease:H00002
NANDO:2200013	http://nanbyodata.jp/ontology/NANDO_2200013	慢性骨髄性白血病	Chronic myeloid leukemia	H00004	http://www.geneontology.org/formats/oboInOwl#hasDbXref	慢性骨髄性白血病	Chronic myeloid leukemia	https://identifiers.org/kegg.disease:H00004
NANDO:2200019	http://nanbyodata.jp/ontology/NANDO_2200019	骨髄異形成症候群	Myelodysplastic syndrome	H01481	http://www.geneontology.org/formats/oboInOwl#hasDbXref	骨髄異形成症候群	Myelodysplastic syndrome	https://identifiers.org/kegg.disease:H01481
NANDO:2200021	http://nanbyodata.jp/ontology/NANDO_2200021	未分化大細胞リンパ腫	Anaplastic large cell lymphoma	H01601	http://www.geneontology.org/formats/oboInOwl#hasDbXref	未分化大細胞リンパ腫	Anaplastic large-cell lymphoma	https://identifiers.org/kegg.disease:H01601
NANDO:2200024	http://nanbyodata.jp/ontology/NANDO_2200024	ホジキンリンパ腫	Hodgkin lymphoma	H00007	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ホジキンリンパ腫	Hodgkin lymphoma	https://identifiers.org/kegg.disease:H00007
NANDO:2200031	http://nanbyodata.jp/ontology/NANDO_2200031	ランゲルハンス細胞組織球症	Langerhans cell histiocytosis	H01512	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ランゲルハンス細胞組織球症	Langerhans cell histiocytosis	https://identifiers.org/kegg.disease:H01512
NANDO:2200040	http://nanbyodata.jp/ontology/NANDO_2200040	神経芽腫	Neuroblastoma	H00043	http://www.geneontology.org/formats/oboInOwl#hasDbXref	神経芽腫	Neuroblastoma	https://identifiers.org/kegg.disease:H00043
NANDO:2200040	http://nanbyodata.jp/ontology/NANDO_2200040	神経芽腫	Neuroblastoma	H00043	http://www.geneontology.org/formats/oboInOwl#hasDbXref	神経芽細胞腫	Neuroblastoma	https://identifiers.org/kegg.disease:H00043
NANDO:2200042	http://nanbyodata.jp/ontology/NANDO_2200042	網膜芽細胞腫	Retinoblastoma	H01513	http://www.geneontology.org/formats/oboInOwl#hasDbXref	網膜芽細胞腫	Retinoblastoma	https://identifiers.org/kegg.disease:H01513
NANDO:2200042	http://nanbyodata.jp/ontology/NANDO_2200042	網膜芽細胞腫	Retinoblastoma	H01513	http://www.geneontology.org/formats/oboInOwl#hasDbXref	網膜芽腫	Retinoblastoma	https://identifiers.org/kegg.disease:H01513
NANDO:2200045	http://nanbyodata.jp/ontology/NANDO_2200045	腎細胞癌	Renal cell carcinoma	H00021	http://www.geneontology.org/formats/oboInOwl#hasDbXref	腎細胞癌	Renal cell carcinoma	https://identifiers.org/kegg.disease:H00021
NANDO:2200047	http://nanbyodata.jp/ontology/NANDO_2200047	肝細胞癌	Hepatocellular carcinoma	H00048	http://www.geneontology.org/formats/oboInOwl#hasDbXref	肝細胞癌	Hepatocellular carcinoma	https://identifiers.org/kegg.disease:H00048
NANDO:2200047	http://nanbyodata.jp/ontology/NANDO_2200047	肝細胞癌	Hepatocellular carcinoma	H00048	http://www.geneontology.org/formats/oboInOwl#hasDbXref	肝癌	Hepatocellular carcinoma	https://identifiers.org/kegg.disease:H00048
NANDO:2200047	http://nanbyodata.jp/ontology/NANDO_2200047	肝細胞癌	Hepatocellular carcinoma	H00048	http://www.geneontology.org/formats/oboInOwl#hasDbXref	肝細胞癌	Liver cancer	https://identifiers.org/kegg.disease:H00048
NANDO:2200047	http://nanbyodata.jp/ontology/NANDO_2200047	肝細胞癌	Hepatocellular carcinoma	H00048	http://www.geneontology.org/formats/oboInOwl#hasDbXref	肝癌	Liver cancer	https://identifiers.org/kegg.disease:H00048
NANDO:2200048	http://nanbyodata.jp/ontology/NANDO_2200048	骨肉腫	Osteosarcoma	H00036	http://www.geneontology.org/formats/oboInOwl#hasDbXref	骨肉腫	Osteosarcoma	https://identifiers.org/kegg.disease:H00036
NANDO:2200053	http://nanbyodata.jp/ontology/NANDO_2200053	ユーイング肉腫	Ewing's sarcoma	H00035	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ユーイング肉腫	Ewing sarcoma	https://identifiers.org/kegg.disease:H00035
NANDO:2200056	http://nanbyodata.jp/ontology/NANDO_2200056	横紋筋肉腫	Rhabdomyosarcoma	H00037	http://www.geneontology.org/formats/oboInOwl#hasDbXref	横紋筋肉腫	Rhabdomyosarcoma	https://identifiers.org/kegg.disease:H00037
NANDO:2200061	http://nanbyodata.jp/ontology/NANDO_2200061	滑膜肉腫	Synovial sarcoma	H00050	http://www.geneontology.org/formats/oboInOwl#hasDbXref	滑膜肉腫	Synovial sarcoma	https://identifiers.org/kegg.disease:H00050
NANDO:2200062	http://nanbyodata.jp/ontology/NANDO_2200062	明細胞肉腫	Clear cell sarcoma	H00052	http://www.geneontology.org/formats/oboInOwl#hasDbXref	明細胞肉腫	Clear cell sarcoma of soft tissue	https://identifiers.org/kegg.disease:H00052
NANDO:2200063	http://nanbyodata.jp/ontology/NANDO_2200063	胞巣状軟部肉腫	Alveolar soft part sarcoma	H00051	http://www.geneontology.org/formats/oboInOwl#hasDbXref	胞巣状軟部肉腫	Alveolar soft part sarcoma	https://identifiers.org/kegg.disease:H00051
NANDO:2200070	http://nanbyodata.jp/ontology/NANDO_2200070	絨毛癌	Choriocarcinoma	H00028	http://www.geneontology.org/formats/oboInOwl#hasDbXref	絨毛癌	Choriocarcinoma	https://identifiers.org/kegg.disease:H00028
NANDO:2200074	http://nanbyodata.jp/ontology/NANDO_2200074	甲状腺癌	Thyroid cancer	H00032	http://www.geneontology.org/formats/oboInOwl#hasDbXref	甲状腺癌	Thyroid cancer	https://identifiers.org/kegg.disease:H00032
NANDO:2200076	http://nanbyodata.jp/ontology/NANDO_2200076	唾液腺癌	Salivary grand carcinoma	H01508	http://www.geneontology.org/formats/oboInOwl#hasDbXref	唾液腺癌	Salivary gland cancer	https://identifiers.org/kegg.disease:H01508
NANDO:2200077	http://nanbyodata.jp/ontology/NANDO_2200077	悪性黒色腫	Malignant melanoma	H00038	http://www.geneontology.org/formats/oboInOwl#hasDbXref	悪性黒色腫	Melanoma	https://identifiers.org/kegg.disease:H00038
NANDO:2200090	http://nanbyodata.jp/ontology/NANDO_2200090	髄芽腫	Medulloblastoma	H01667	http://www.geneontology.org/formats/oboInOwl#hasDbXref	髄芽腫	Medulloblastoma	https://identifiers.org/kegg.disease:H01667
NANDO:2200093	http://nanbyodata.jp/ontology/NANDO_2200093	脈絡叢乳頭腫	Choroid plexus papilloma	H01007	http://www.geneontology.org/formats/oboInOwl#hasDbXref	脈絡叢乳頭腫	Choroid plexus papilloma	https://identifiers.org/kegg.disease:H01007
NANDO:2200094	http://nanbyodata.jp/ontology/NANDO_2200094	髄膜腫	Meningioma	H01556	http://www.geneontology.org/formats/oboInOwl#hasDbXref	髄膜腫	Meningioma	https://identifiers.org/kegg.disease:H01556
NANDO:2200095	http://nanbyodata.jp/ontology/NANDO_2200095	下垂体腺腫	Pituitary adenoma	H01102	http://www.geneontology.org/formats/oboInOwl#hasDbXref	下垂体腺腫	Pituitary adenomas	https://identifiers.org/kegg.disease:H01102
NANDO:2200113	http://nanbyodata.jp/ontology/NANDO_2200113	巣状分節性糸球体硬化症	Focal segmental glomerulosclerosis	H00626	http://www.geneontology.org/formats/oboInOwl#hasDbXref	巣状分節性糸球体硬化症	Focal segmental glomerulosclerosis	https://identifiers.org/kegg.disease:H00626
NANDO:2200117	http://nanbyodata.jp/ontology/NANDO_2200117	Pierson症候群	Pierson syndrome	H00576	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ピアソン症候群	Pierson syndrome	https://identifiers.org/kegg.disease:H00576
NANDO:2200121	http://nanbyodata.jp/ontology/NANDO_2200121	IgA腎症	IgA nephropathy	H01581	http://www.geneontology.org/formats/oboInOwl#hasDbXref	IgA 腎症	IgA nephropathy	https://identifiers.org/kegg.disease:H01581
NANDO:2200121	http://nanbyodata.jp/ontology/NANDO_2200121	IgA腎症	IgA nephropathy	H01581	http://www.geneontology.org/formats/oboInOwl#hasDbXref	IgA 腎症	Berger disease	https://identifiers.org/kegg.disease:H01581
NANDO:2200123	http://nanbyodata.jp/ontology/NANDO_2200123	膜性増殖性糸球体腎炎	Membranoproliferative glomerulonephritis	H01726	http://www.geneontology.org/formats/oboInOwl#hasDbXref	膜性増殖性糸球体腎炎	Membranoproliferative glomerulonephritis	https://identifiers.org/kegg.disease:H01726
NANDO:2200124	http://nanbyodata.jp/ontology/NANDO_2200124	紫斑病性腎炎	Henoch-Schonlein purpura nephritis	H01767	http://www.geneontology.org/formats/oboInOwl#hasDbXref	紫斑病性腎炎	Henoch-Schonlein purpura nephritis	https://identifiers.org/kegg.disease:H01767
NANDO:2200125	http://nanbyodata.jp/ontology/NANDO_2200125	抗糸球体基底膜腎炎	Goodpasture syndrome	H01721	http://www.geneontology.org/formats/oboInOwl#hasDbXref	グッドパスチャー症候群	Goodpasture syndrome	https://identifiers.org/kegg.disease:H01721
NANDO:2200125	http://nanbyodata.jp/ontology/NANDO_2200125	抗糸球体基底膜腎炎	Goodpasture syndrome	H01721	http://www.geneontology.org/formats/oboInOwl#hasDbXref	抗糸球体基底膜腎炎	Goodpasture syndrome	https://identifiers.org/kegg.disease:H01721
NANDO:2200125	http://nanbyodata.jp/ontology/NANDO_2200125	抗糸球体基底膜腎炎	Goodpasture syndrome	H01721	http://www.geneontology.org/formats/oboInOwl#hasDbXref	グッドパスチャー症候群	Anti-glomerular basement membrane (GBM) disease	https://identifiers.org/kegg.disease:H01721
NANDO:2200125	http://nanbyodata.jp/ontology/NANDO_2200125	抗糸球体基底膜腎炎	Goodpasture syndrome	H01721	http://www.geneontology.org/formats/oboInOwl#hasDbXref	抗糸球体基底膜腎炎	Anti-glomerular basement membrane (GBM) disease	https://identifiers.org/kegg.disease:H01721
NANDO:2200126	http://nanbyodata.jp/ontology/NANDO_2200126	慢性糸球体腎炎（アルポート 症候群によるものに限る。）	Alport syndrome	H00581	http://www.geneontology.org/formats/oboInOwl#hasDbXref	アルポート症候群	Alport syndrome	https://identifiers.org/kegg.disease:H00581
NANDO:2200127	http://nanbyodata.jp/ontology/NANDO_2200127	エプスタイン症候群	Epstein syndrome	H00578	http://www.geneontology.org/formats/oboInOwl#hasDbXref	エプスタイン症候群	Epstein syndrome	https://identifiers.org/kegg.disease:H00578
NANDO:2200128	http://nanbyodata.jp/ontology/NANDO_2200128	ループス腎炎	Lupus nephritis	H01500	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ループス腎炎	Lupus nephritis	https://identifiers.org/kegg.disease:H01500
NANDO:2200131	http://nanbyodata.jp/ontology/NANDO_2200131	非典型溶血性尿毒症症候群	Atypical hemolytic uremic syndrome	H01434	http://www.geneontology.org/formats/oboInOwl#hasDbXref	非典型溶血性尿毒症症候群	Atypical hemolytic uremic syndrome	https://identifiers.org/kegg.disease:H01434
NANDO:2200132	http://nanbyodata.jp/ontology/NANDO_2200132	ネイル・パテラ症候群	Nail-patella syndrome	H00464	http://www.geneontology.org/formats/oboInOwl#hasDbXref	爪膝蓋骨症候群	Nail-patella syndrome	https://identifiers.org/kegg.disease:H00464
NANDO:2200133	http://nanbyodata.jp/ontology/NANDO_2200133	フィブロネクチン腎症	Glomerulopathy with fibronectin deposits, fibronectin nephropathy	H01260	http://www.geneontology.org/formats/oboInOwl#hasDbXref	フィブロネクチン腎症	Glomerulopathy with fibronectin deposits	https://identifiers.org/kegg.disease:H01260
NANDO:2200134	http://nanbyodata.jp/ontology/NANDO_2200134	リポタンパク糸球体症	Lipoprotein glomerulopathy	H00887	http://www.geneontology.org/formats/oboInOwl#hasDbXref	リポ蛋白糸球体症	Lipoprotein glomerulopathy	https://identifiers.org/kegg.disease:H00887
NANDO:2200140	http://nanbyodata.jp/ontology/NANDO_2200140	ネフロン癆	Nephronophthisis	H00537	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ネフロン癆	Nephronophthisis	https://identifiers.org/kegg.disease:H00537
NANDO:2200145	http://nanbyodata.jp/ontology/NANDO_2200145	ギッテルマン症候群	Gitelman syndrome	H00240	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ギテルマン症候群	Gitelman syndrome	https://identifiers.org/kegg.disease:H00240
NANDO:2200146	http://nanbyodata.jp/ontology/NANDO_2200146	バーター症候群	Bartter syndrome	H00239	http://www.geneontology.org/formats/oboInOwl#hasDbXref	バーター症候群	Bartter syndrome	https://identifiers.org/kegg.disease:H00239
NANDO:2200152	http://nanbyodata.jp/ontology/NANDO_2200152	多発性嚢胞腎	Polycystic kidney disease	H00542	http://www.geneontology.org/formats/oboInOwl#hasDbXref	多発性嚢胞腎	Polycystic kidney disease	https://identifiers.org/kegg.disease:H00542
NANDO:2200179	http://nanbyodata.jp/ontology/NANDO_2200179	膀胱尿管逆流	Vesicoureteral reflux	H01037	http://www.geneontology.org/formats/oboInOwl#hasDbXref	膀胱尿管逆流	Vesicoureteral reflux	https://identifiers.org/kegg.disease:H01037
NANDO:2200188	http://nanbyodata.jp/ontology/NANDO_2200188	ロウ症候群	Lowe syndrome	H00692	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ロウ症候群	Lowe syndrome	https://identifiers.org/kegg.disease:H00692
NANDO:2200188	http://nanbyodata.jp/ontology/NANDO_2200188	ロウ症候群	Lowe syndrome	H00692	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ロウ症候群	Oculocerebrorenal Dystrophy (OCRL)	https://identifiers.org/kegg.disease:H00692
NANDO:2200198	http://nanbyodata.jp/ontology/NANDO_2200198	先天性中枢性低換気症候群	Congenital central hypoventilation syndrome	H00916	http://www.geneontology.org/formats/oboInOwl#hasDbXref	先天性中枢性低換気症候群	Congenital central hypoventilation syndrome	https://identifiers.org/kegg.disease:H00916
NANDO:2200199	http://nanbyodata.jp/ontology/NANDO_2200199	特発性間質性肺炎	Idiopathic interstitial pneumonia	H01716	http://www.geneontology.org/formats/oboInOwl#hasDbXref	特発性間質性肺炎	Idiopathic interstitial pneumonias	https://identifiers.org/kegg.disease:H01716
NANDO:2200200	http://nanbyodata.jp/ontology/NANDO_2200200	先天性肺胞蛋白症	Congenital alveolar proteinosis	H01122	http://www.geneontology.org/formats/oboInOwl#hasDbXref	先天性肺胞蛋白症	Congenital pulmonary alveolar proteinosis	https://identifiers.org/kegg.disease:H01122
NANDO:2200200	http://nanbyodata.jp/ontology/NANDO_2200200	先天性肺胞蛋白症	Congenital alveolar proteinosis	H01122	http://www.geneontology.org/formats/oboInOwl#hasDbXref	肺サーファクタント代謝異常症	Congenital pulmonary alveolar proteinosis	https://identifiers.org/kegg.disease:H01122
NANDO:2200200	http://nanbyodata.jp/ontology/NANDO_2200200	先天性肺胞蛋白症	Congenital alveolar proteinosis	H01122	http://www.geneontology.org/formats/oboInOwl#hasDbXref	先天性肺胞蛋白症	Pulmonary surfactant metabolism dysfunction	https://identifiers.org/kegg.disease:H01122
NANDO:2200200	http://nanbyodata.jp/ontology/NANDO_2200200	先天性肺胞蛋白症	Congenital alveolar proteinosis	H01122	http://www.geneontology.org/formats/oboInOwl#hasDbXref	肺サーファクタント代謝異常症	Pulmonary surfactant metabolism dysfunction	https://identifiers.org/kegg.disease:H01122
NANDO:2200202	http://nanbyodata.jp/ontology/NANDO_2200202	肺胞微石症	Pulmonary alveolar microlithiasis	H01298	http://www.geneontology.org/formats/oboInOwl#hasDbXref	肺胞微石症	Pulmonary alveolar microlithiasis	https://identifiers.org/kegg.disease:H01298
NANDO:2200205	http://nanbyodata.jp/ontology/NANDO_2200205	嚢胞性線維症	Cystic fibrosis	H00218	http://www.geneontology.org/formats/oboInOwl#hasDbXref	嚢胞性線維症	Cystic fibrosis	https://identifiers.org/kegg.disease:H00218
NANDO:2200206	http://nanbyodata.jp/ontology/NANDO_2200206	気管支拡張症	Bronchiectasis	H00892	http://www.geneontology.org/formats/oboInOwl#hasDbXref	気管支拡張症	Bronchiectasis with or without elevated sweat chloride	https://identifiers.org/kegg.disease:H00892
NANDO:2200210	http://nanbyodata.jp/ontology/NANDO_2200210	先天性横隔膜ヘルニア	Congenital diaphragmatic hernia	H01241	http://www.geneontology.org/formats/oboInOwl#hasDbXref	先天性横隔膜ヘルニア	Congenital diaphragmatic hernia	https://identifiers.org/kegg.disease:H01241
NANDO:2200212	http://nanbyodata.jp/ontology/NANDO_2200212	洞不全症候群	Sick sinus syndrome	H00729	http://www.geneontology.org/formats/oboInOwl#hasDbXref	洞不全症候群	Sick sinus syndrome	https://identifiers.org/kegg.disease:H00729
NANDO:2200212	http://nanbyodata.jp/ontology/NANDO_2200212	洞不全症候群	Sick sinus syndrome	H00729	http://www.geneontology.org/formats/oboInOwl#hasDbXref	洞不全症候群	Sinus node dysfunction	https://identifiers.org/kegg.disease:H00729
NANDO:2200221	http://nanbyodata.jp/ontology/NANDO_2200221	カテコラミン誘発多形性心室頻拍	Catecholaminergic polymorphic ventricular tachycardia	H01019	http://www.geneontology.org/formats/oboInOwl#hasDbXref	カテコールアミン誘発性多形性心室頻拍	Catecholaminergic polymorphic ventricular tachycardia	https://identifiers.org/kegg.disease:H01019
NANDO:2200226	http://nanbyodata.jp/ontology/NANDO_2200226	心房細動	Atrial fibrillation	H00731	http://www.geneontology.org/formats/oboInOwl#hasDbXref	心房細動	Atrial fibrillation	https://identifiers.org/kegg.disease:H00731
NANDO:2200228	http://nanbyodata.jp/ontology/NANDO_2200228	QT延長症候群	Long qt syndrome	H00720	http://www.geneontology.org/formats/oboInOwl#hasDbXref	QT 延長症候群	Long QT syndrome	https://identifiers.org/kegg.disease:H00720
NANDO:2200229	http://nanbyodata.jp/ontology/NANDO_2200229	肥大型心筋症	Hypertrophic cardiomyopathy	H00292	http://www.geneontology.org/formats/oboInOwl#hasDbXref	肥大型心筋症	Hypertrophic cardiomyopathy	https://identifiers.org/kegg.disease:H00292
NANDO:2200230	http://nanbyodata.jp/ontology/NANDO_2200230	不整脈源性右室心筋症	Arrhythmogenic right ventricular cardiomyopathy or dysplasia	H00293	http://www.geneontology.org/formats/oboInOwl#hasDbXref	不整脈源性右室心筋症	Arrhythmogenic right ventricular cardiomyopathy	https://identifiers.org/kegg.disease:H00293
NANDO:2200232	http://nanbyodata.jp/ontology/NANDO_2200232	拡張型心筋症	Dilated cardiomyopathy	H00294	http://www.geneontology.org/formats/oboInOwl#hasDbXref	拡張型心筋症	Dilated cardiomyopathy	https://identifiers.org/kegg.disease:H00294
NANDO:2200233	http://nanbyodata.jp/ontology/NANDO_2200233	拘束型心筋症	Restrictive cardiomyopathy	H01219	http://www.geneontology.org/formats/oboInOwl#hasDbXref	拘束性心筋症	Restrictive cardiomyopathy	https://identifiers.org/kegg.disease:H01219
NANDO:2200247	http://nanbyodata.jp/ontology/NANDO_2200247	狭心症	Angina pectoris	H01632	http://www.geneontology.org/formats/oboInOwl#hasDbXref	狭心症	Angina pectoris	https://identifiers.org/kegg.disease:H01632
NANDO:2200248	http://nanbyodata.jp/ontology/NANDO_2200248	心筋梗塞	Myocardial infarction	H01730	http://www.geneontology.org/formats/oboInOwl#hasDbXref	心筋梗塞	Myocardial infarction	https://identifiers.org/kegg.disease:H01730
NANDO:2200249	http://nanbyodata.jp/ontology/NANDO_2200249	左心低形成症候群	Hypoplastic left heart syndrome	H01272	http://www.geneontology.org/formats/oboInOwl#hasDbXref	左心低形成症候群	Hypoplastic left heart syndrome	https://identifiers.org/kegg.disease:H01272
NANDO:2200250	http://nanbyodata.jp/ontology/NANDO_2200250	単心室症	Single ventricle	H01787	http://www.geneontology.org/formats/oboInOwl#hasDbXref	単心室症	Univentricular heart	https://identifiers.org/kegg.disease:H01787
NANDO:2200251	http://nanbyodata.jp/ontology/NANDO_2200251	三尖弁閉鎖症	Tricuspid atresia	H01785	http://www.geneontology.org/formats/oboInOwl#hasDbXref	三尖弁閉鎖症	Tricuspid atresia	https://identifiers.org/kegg.disease:H01785
NANDO:2200252	http://nanbyodata.jp/ontology/NANDO_2200252	心室中隔欠損を伴う肺動脈閉鎖症	Pulmonary atresia with ventricular septal defect	H01803	http://www.geneontology.org/formats/oboInOwl#hasDbXref	心室中隔欠損を伴う肺動脈閉鎖症	Pulmonary atresia with ventricular septal defect	https://identifiers.org/kegg.disease:H01803
NANDO:2200253	http://nanbyodata.jp/ontology/NANDO_2200253	心室中隔欠損を伴わない肺動脈閉鎖症	Pulmonary atresia with intact ventricular septum	H01802	http://www.geneontology.org/formats/oboInOwl#hasDbXref	心室中隔欠損を伴わない肺動脈閉鎖症	Pulmonary atresia with intact ventricular septum	https://identifiers.org/kegg.disease:H01802
NANDO:2200254	http://nanbyodata.jp/ontology/NANDO_2200254	ファロー四徴症	Tetralogy of Fallot	H00549	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ファロー四徴症	Tetralogy of Fallot	https://identifiers.org/kegg.disease:H00549
NANDO:2200256	http://nanbyodata.jp/ontology/NANDO_2200256	両大血管右室起始症	Double outlet right ventricle	H00918	http://www.geneontology.org/formats/oboInOwl#hasDbXref	両大血管右室起始症	Double-outlet right ventricle	https://identifiers.org/kegg.disease:H00918
NANDO:2200258	http://nanbyodata.jp/ontology/NANDO_2200258	完全大血管転位症	Complete transposition of the great arteries	H00550	http://www.geneontology.org/formats/oboInOwl#hasDbXref	完全大血管転位症	Complete transposition of the great arteries	https://identifiers.org/kegg.disease:H00550
NANDO:2200260	http://nanbyodata.jp/ontology/NANDO_2200260	エプスタイン病	Ebstein's anomaly	H01783	http://www.geneontology.org/formats/oboInOwl#hasDbXref	エプスタイン病	Ebstein anomaly	https://identifiers.org/kegg.disease:H01783
NANDO:2200261	http://nanbyodata.jp/ontology/NANDO_2200261	総動脈幹遺残症	Truncus arteriosus communis	H01736	http://www.geneontology.org/formats/oboInOwl#hasDbXref	総動脈幹遺残症	Persistent truncus arteriosus	https://identifiers.org/kegg.disease:H01736
NANDO:2200264	http://nanbyodata.jp/ontology/NANDO_2200264	動脈管開存症	Patent ductus arteriosus	H01630	http://www.geneontology.org/formats/oboInOwl#hasDbXref	動脈管開存症	Patent ductus arteriosus	https://identifiers.org/kegg.disease:H01630
NANDO:2200286	http://nanbyodata.jp/ontology/NANDO_2200286	ウィリアムズ症候群	Williams syndrome	H01439	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ウィリアムズ症候群	Williams-Beuren syndrome	https://identifiers.org/kegg.disease:H01439
NANDO:2200298	http://nanbyodata.jp/ontology/NANDO_2200298	肺動脈性肺高血圧症	Pulmonary arterial hypertension	H01621	http://www.geneontology.org/formats/oboInOwl#hasDbXref	肺動脈性肺高血圧症	Pulmonary arterial hypertension	https://identifiers.org/kegg.disease:H01621
NANDO:2200310	http://nanbyodata.jp/ontology/NANDO_2200310	多脾症候群	Polysplenia syndrome	H01764	http://www.geneontology.org/formats/oboInOwl#hasDbXref	多脾症候群	Polysplenia syndrome	https://identifiers.org/kegg.disease:H01764
NANDO:2200314	http://nanbyodata.jp/ontology/NANDO_2200314	下垂体性巨人症	Pituitary gigantism	H01618	http://www.geneontology.org/formats/oboInOwl#hasDbXref	下垂体性巨人症	Pituitary gigantism	https://identifiers.org/kegg.disease:H01618
NANDO:2200315	http://nanbyodata.jp/ontology/NANDO_2200315	先端巨大症	Acromegaly	H01483	http://www.geneontology.org/formats/oboInOwl#hasDbXref	先端巨大症	Acromegaly	https://identifiers.org/kegg.disease:H01483
NANDO:2200322	http://nanbyodata.jp/ontology/NANDO_2200322	高プロラクチン血症	Hyperprolactinemia	H01388	http://www.geneontology.org/formats/oboInOwl#hasDbXref	高プロラクチン血症	Hyperprolactinemia	https://identifiers.org/kegg.disease:H01388
NANDO:2200322	http://nanbyodata.jp/ontology/NANDO_2200322	高プロラクチン血症	Hyperprolactinemia	H01388	http://www.geneontology.org/formats/oboInOwl#hasDbXref	下垂体性 PRL 分泌亢進症	Hyperprolactinemia	https://identifiers.org/kegg.disease:H01388
NANDO:2200324	http://nanbyodata.jp/ontology/NANDO_2200324	中枢性尿崩症	Central diabetes insipidus	H00253	http://www.geneontology.org/formats/oboInOwl#hasDbXref	中枢性尿崩症	Central diabetes insipidus	https://identifiers.org/kegg.disease:H00253
NANDO:2200324	http://nanbyodata.jp/ontology/NANDO_2200324	中枢性尿崩症	Central diabetes insipidus	H00253	http://www.geneontology.org/formats/oboInOwl#hasDbXref	神経下垂体性尿崩症	Central diabetes insipidus	https://identifiers.org/kegg.disease:H00253
NANDO:2200324	http://nanbyodata.jp/ontology/NANDO_2200324	中枢性尿崩症	Central diabetes insipidus	H00253	http://www.geneontology.org/formats/oboInOwl#hasDbXref	中枢性尿崩症	Neurohypophyseal diabetes insipidus	https://identifiers.org/kegg.disease:H00253
NANDO:2200324	http://nanbyodata.jp/ontology/NANDO_2200324	中枢性尿崩症	Central diabetes insipidus	H00253	http://www.geneontology.org/formats/oboInOwl#hasDbXref	神経下垂体性尿崩症	Neurohypophyseal diabetes insipidus	https://identifiers.org/kegg.disease:H00253
NANDO:2200329	http://nanbyodata.jp/ontology/NANDO_2200329	甲状腺機能亢進症	Hyperthyroidism	H01645	http://www.geneontology.org/formats/oboInOwl#hasDbXref	甲状腺機能亢進症	Hyperthyroidism	https://identifiers.org/kegg.disease:H01645
NANDO:2200329	http://nanbyodata.jp/ontology/NANDO_2200329	甲状腺機能亢進症	Hyperthyroidism	H01645	http://www.geneontology.org/formats/oboInOwl#hasDbXref	甲状腺中毒症	Hyperthyroidism	https://identifiers.org/kegg.disease:H01645
NANDO:2200329	http://nanbyodata.jp/ontology/NANDO_2200329	甲状腺機能亢進症	Hyperthyroidism	H01645	http://www.geneontology.org/formats/oboInOwl#hasDbXref	甲状腺機能亢進症	Thyrotoxicosis	https://identifiers.org/kegg.disease:H01645
NANDO:2200329	http://nanbyodata.jp/ontology/NANDO_2200329	甲状腺機能亢進症	Hyperthyroidism	H01645	http://www.geneontology.org/formats/oboInOwl#hasDbXref	甲状腺中毒症	Thyrotoxicosis	https://identifiers.org/kegg.disease:H01645
NANDO:2200335	http://nanbyodata.jp/ontology/NANDO_2200335	橋本病	Hashimoto disease	H00081	http://www.geneontology.org/formats/oboInOwl#hasDbXref	橋本病	Hashimoto thyroiditis	https://identifiers.org/kegg.disease:H00081
NANDO:2200343	http://nanbyodata.jp/ontology/NANDO_2200343	副甲状腺機能亢進症	Hyperparathyroidism	H00246	http://www.geneontology.org/formats/oboInOwl#hasDbXref	副甲状腺機能亢進症	Familial hyperparathyroidism	https://identifiers.org/kegg.disease:H00246
NANDO:2200343	http://nanbyodata.jp/ontology/NANDO_2200343	副甲状腺機能亢進症	Hyperparathyroidism	H00246	http://www.geneontology.org/formats/oboInOwl#hasDbXref	副甲状腺機能亢進症	Primary hyperparathyroidism	https://identifiers.org/kegg.disease:H00246
NANDO:2200345	http://nanbyodata.jp/ontology/NANDO_2200345	副甲状腺機能低下症	Hypoparathyroidism	H01862	http://www.geneontology.org/formats/oboInOwl#hasDbXref	副甲状腺機能低下症	Hypoparathyroidism	https://identifiers.org/kegg.disease:H01862
NANDO:2200349	http://nanbyodata.jp/ontology/NANDO_2200349	偽性副甲状腺機能低下症	Pseudohypoparathyroidism	H00244	http://www.geneontology.org/formats/oboInOwl#hasDbXref	偽性副甲状腺機能低下症	Pseudohypoparathyroidism	https://identifiers.org/kegg.disease:H00244
NANDO:2200356	http://nanbyodata.jp/ontology/NANDO_2200356	副腎皮質刺激ホルモン不応症	ACTH unresponsiveness	H00256	http://www.geneontology.org/formats/oboInOwl#hasDbXref	副腎皮質刺激ホルモン不応症	Familial glucocorticoid deficiency	https://identifiers.org/kegg.disease:H00256
NANDO:2200356	http://nanbyodata.jp/ontology/NANDO_2200356	副腎皮質刺激ホルモン不応症	ACTH unresponsiveness	H00256	http://www.geneontology.org/formats/oboInOwl#hasDbXref	家族性糖質コルチコイド欠損症	Familial glucocorticoid deficiency	https://identifiers.org/kegg.disease:H00256
NANDO:2200357	http://nanbyodata.jp/ontology/NANDO_2200357	先天性副腎低形成症	Congenital adrenal hypoplasia	H01772	http://www.geneontology.org/formats/oboInOwl#hasDbXref	先天性副腎低形成症	Adrenal hypoplasia, congenital	https://identifiers.org/kegg.disease:H01772
NANDO:2200357	http://nanbyodata.jp/ontology/NANDO_2200357	先天性副腎低形成症	Congenital adrenal hypoplasia	H01772	http://www.geneontology.org/formats/oboInOwl#hasDbXref	X連鎖性アジソン病	Adrenal hypoplasia, congenital	https://identifiers.org/kegg.disease:H01772
NANDO:2200357	http://nanbyodata.jp/ontology/NANDO_2200357	先天性副腎低形成症	Congenital adrenal hypoplasia	H01772	http://www.geneontology.org/formats/oboInOwl#hasDbXref	先天性副腎低形成症	X-linked addison disease	https://identifiers.org/kegg.disease:H01772
NANDO:2200357	http://nanbyodata.jp/ontology/NANDO_2200357	先天性副腎低形成症	Congenital adrenal hypoplasia	H01772	http://www.geneontology.org/formats/oboInOwl#hasDbXref	X連鎖性アジソン病	X-linked addison disease	https://identifiers.org/kegg.disease:H01772
NANDO:2200360	http://nanbyodata.jp/ontology/NANDO_2200360	アジソン病	Addison's disease	H01598	http://www.geneontology.org/formats/oboInOwl#hasDbXref	アジソン病	Addison disease	https://identifiers.org/kegg.disease:H01598
NANDO:2200360	http://nanbyodata.jp/ontology/NANDO_2200360	アジソン病	Addison's disease	H01598	http://www.geneontology.org/formats/oboInOwl#hasDbXref	副腎機能低下症	Addison disease	https://identifiers.org/kegg.disease:H01598
NANDO:2200360	http://nanbyodata.jp/ontology/NANDO_2200360	アジソン病	Addison's disease	H01598	http://www.geneontology.org/formats/oboInOwl#hasDbXref	原発性副腎機能不全	Addison disease	https://identifiers.org/kegg.disease:H01598
NANDO:2200360	http://nanbyodata.jp/ontology/NANDO_2200360	アジソン病	Addison's disease	H01598	http://www.geneontology.org/formats/oboInOwl#hasDbXref	アジソン病	Hypoadrenocorticism	https://identifiers.org/kegg.disease:H01598
NANDO:2200360	http://nanbyodata.jp/ontology/NANDO_2200360	アジソン病	Addison's disease	H01598	http://www.geneontology.org/formats/oboInOwl#hasDbXref	副腎機能低下症	Hypoadrenocorticism	https://identifiers.org/kegg.disease:H01598
NANDO:2200360	http://nanbyodata.jp/ontology/NANDO_2200360	アジソン病	Addison's disease	H01598	http://www.geneontology.org/formats/oboInOwl#hasDbXref	原発性副腎機能不全	Hypoadrenocorticism	https://identifiers.org/kegg.disease:H01598
NANDO:2200360	http://nanbyodata.jp/ontology/NANDO_2200360	アジソン病	Addison's disease	H01598	http://www.geneontology.org/formats/oboInOwl#hasDbXref	アジソン病	Primary adrenal insufficiency	https://identifiers.org/kegg.disease:H01598
NANDO:2200360	http://nanbyodata.jp/ontology/NANDO_2200360	アジソン病	Addison's disease	H01598	http://www.geneontology.org/formats/oboInOwl#hasDbXref	副腎機能低下症	Primary adrenal insufficiency	https://identifiers.org/kegg.disease:H01598
NANDO:2200360	http://nanbyodata.jp/ontology/NANDO_2200360	アジソン病	Addison's disease	H01598	http://www.geneontology.org/formats/oboInOwl#hasDbXref	原発性副腎機能不全	Primary adrenal insufficiency	https://identifiers.org/kegg.disease:H01598
NANDO:2200362	http://nanbyodata.jp/ontology/NANDO_2200362	見かけの鉱質コルチコイド過剰症候群	Apparent mineralocorticoid excess syndrome	H00259	http://www.geneontology.org/formats/oboInOwl#hasDbXref	AME 症候群	Apparent mineralocorticoid excess syndrome	https://identifiers.org/kegg.disease:H00259
NANDO:2200362	http://nanbyodata.jp/ontology/NANDO_2200362	見かけの鉱質コルチコイド過剰症候群	Apparent mineralocorticoid excess syndrome	H00259	http://www.geneontology.org/formats/oboInOwl#hasDbXref	11β-ヒドロキシステロイドデヒドロゲナーゼ欠損症	Apparent mineralocorticoid excess syndrome	https://identifiers.org/kegg.disease:H00259
NANDO:2200362	http://nanbyodata.jp/ontology/NANDO_2200362	見かけの鉱質コルチコイド過剰症候群	Apparent mineralocorticoid excess syndrome	H00259	http://www.geneontology.org/formats/oboInOwl#hasDbXref	AME 症候群	11-beta-ketoreductase deficiency	https://identifiers.org/kegg.disease:H00259
NANDO:2200362	http://nanbyodata.jp/ontology/NANDO_2200362	見かけの鉱質コルチコイド過剰症候群	Apparent mineralocorticoid excess syndrome	H00259	http://www.geneontology.org/formats/oboInOwl#hasDbXref	11β-ヒドロキシステロイドデヒドロゲナーゼ欠損症	11-beta-ketoreductase deficiency	https://identifiers.org/kegg.disease:H00259
NANDO:2200363	http://nanbyodata.jp/ontology/NANDO_2200363	リドル症候群	Liddle syndrome	H00242	http://www.geneontology.org/formats/oboInOwl#hasDbXref	リドル症候群	Liddle syndrome	https://identifiers.org/kegg.disease:H00242
NANDO:2200365	http://nanbyodata.jp/ontology/NANDO_2200365	アルドステロン合成酵素欠損症	Aldosterone synthase deficiency	H00258	http://www.geneontology.org/formats/oboInOwl#hasDbXref	アルドステロン合成酵素欠損症	Aldosterone synthase deficiency	https://identifiers.org/kegg.disease:H00258
NANDO:2200365	http://nanbyodata.jp/ontology/NANDO_2200365	アルドステロン合成酵素欠損症	Aldosterone synthase deficiency	H00258	http://www.geneontology.org/formats/oboInOwl#hasDbXref	先天性副腎皮質酵素欠損症	Aldosterone synthase deficiency	https://identifiers.org/kegg.disease:H00258
NANDO:2200365	http://nanbyodata.jp/ontology/NANDO_2200365	アルドステロン合成酵素欠損症	Aldosterone synthase deficiency	H00258	http://www.geneontology.org/formats/oboInOwl#hasDbXref	アルドステロン合成酵素欠損症	Corticosterone methyloxidase type I deficiency	https://identifiers.org/kegg.disease:H00258
NANDO:2200365	http://nanbyodata.jp/ontology/NANDO_2200365	アルドステロン合成酵素欠損症	Aldosterone synthase deficiency	H00258	http://www.geneontology.org/formats/oboInOwl#hasDbXref	先天性副腎皮質酵素欠損症	Corticosterone methyloxidase type I deficiency	https://identifiers.org/kegg.disease:H00258
NANDO:2200365	http://nanbyodata.jp/ontology/NANDO_2200365	アルドステロン合成酵素欠損症	Aldosterone synthase deficiency	H00258	http://www.geneontology.org/formats/oboInOwl#hasDbXref	アルドステロン合成酵素欠損症	Corticosterone methyloxidase type II deficiency	https://identifiers.org/kegg.disease:H00258
NANDO:2200365	http://nanbyodata.jp/ontology/NANDO_2200365	アルドステロン合成酵素欠損症	Aldosterone synthase deficiency	H00258	http://www.geneontology.org/formats/oboInOwl#hasDbXref	先天性副腎皮質酵素欠損症	Corticosterone methyloxidase type II deficiency	https://identifiers.org/kegg.disease:H00258
NANDO:2200382	http://nanbyodata.jp/ontology/NANDO_2200382	低ゴナドトロピン性性腺機能低下症	Hypogonadotropic hypogonadism	H00255	http://www.geneontology.org/formats/oboInOwl#hasDbXref	低ゴナドトロピン性性腺機能低下症	Hypogonadotropic hypogonadism	https://identifiers.org/kegg.disease:H00255
NANDO:2200384	http://nanbyodata.jp/ontology/NANDO_2200384	卵巣形成不全	Ovarian dysgenesis	H00599	http://www.geneontology.org/formats/oboInOwl#hasDbXref	卵巣形成不全	Ovarian dysgenesis	https://identifiers.org/kegg.disease:H00599
NANDO:2200384	http://nanbyodata.jp/ontology/NANDO_2200384	卵巣形成不全	Ovarian dysgenesis	H00599	http://www.geneontology.org/formats/oboInOwl#hasDbXref	46,XX 性腺形成不全症	Ovarian dysgenesis	https://identifiers.org/kegg.disease:H00599
NANDO:2200384	http://nanbyodata.jp/ontology/NANDO_2200384	卵巣形成不全	Ovarian dysgenesis	H00599	http://www.geneontology.org/formats/oboInOwl#hasDbXref	卵巣形成不全	46,XX gonadal dysgenesis	https://identifiers.org/kegg.disease:H00599
NANDO:2200384	http://nanbyodata.jp/ontology/NANDO_2200384	卵巣形成不全	Ovarian dysgenesis	H00599	http://www.geneontology.org/formats/oboInOwl#hasDbXref	46,XX 性腺形成不全症	46,XX gonadal dysgenesis	https://identifiers.org/kegg.disease:H00599
NANDO:2200401	http://nanbyodata.jp/ontology/NANDO_2200401	ビタミンD依存性くる病	Vitamin D-dependent rickets	H01143	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ビタミンD依存性くる病	Vitamin D-dependent rickets	https://identifiers.org/kegg.disease:H01143
NANDO:2200404	http://nanbyodata.jp/ontology/NANDO_2200404	脂肪萎縮症	Lipodystrophy	H01475	http://www.geneontology.org/formats/oboInOwl#hasDbXref	脂肪異栄養症	Lipodystrophy	https://identifiers.org/kegg.disease:H01475
NANDO:2200404	http://nanbyodata.jp/ontology/NANDO_2200404	脂肪萎縮症	Lipodystrophy	H01475	http://www.geneontology.org/formats/oboInOwl#hasDbXref	脂肪萎縮症	Lipodystrophy	https://identifiers.org/kegg.disease:H01475
NANDO:2200404	http://nanbyodata.jp/ontology/NANDO_2200404	脂肪萎縮症	Lipodystrophy	H01475	http://www.geneontology.org/formats/oboInOwl#hasDbXref	リポジストロフィー	Lipodystrophy	https://identifiers.org/kegg.disease:H01475
NANDO:2200404	http://nanbyodata.jp/ontology/NANDO_2200404	脂肪萎縮症	Lipodystrophy	H01475	http://www.geneontology.org/formats/oboInOwl#hasDbXref	脂肪異栄養症	Lipoatrophy	https://identifiers.org/kegg.disease:H01475
NANDO:2200404	http://nanbyodata.jp/ontology/NANDO_2200404	脂肪萎縮症	Lipodystrophy	H01475	http://www.geneontology.org/formats/oboInOwl#hasDbXref	脂肪萎縮症	Lipoatrophy	https://identifiers.org/kegg.disease:H01475
NANDO:2200404	http://nanbyodata.jp/ontology/NANDO_2200404	脂肪萎縮症	Lipodystrophy	H01475	http://www.geneontology.org/formats/oboInOwl#hasDbXref	リポジストロフィー	Lipoatrophy	https://identifiers.org/kegg.disease:H01475
NANDO:2200409	http://nanbyodata.jp/ontology/NANDO_2200409	多嚢胞性卵巣症候群	Polycystic ovary syndrome	H01739	http://www.geneontology.org/formats/oboInOwl#hasDbXref	多嚢胞性卵巣症候群	Polycystic ovary syndrome	https://identifiers.org/kegg.disease:H01739
NANDO:2200411	http://nanbyodata.jp/ontology/NANDO_2200411	プラダー・ウィリ症候群	Prader-Willi syndrome	H00478	http://www.geneontology.org/formats/oboInOwl#hasDbXref	プラダー・ウィリー症候群	Prader-Willi syndrome	https://identifiers.org/kegg.disease:H00478
NANDO:2200412	http://nanbyodata.jp/ontology/NANDO_2200412	マッキューン・オルブライト症候群	McCune-Albright syndrome	H00501	http://www.geneontology.org/formats/oboInOwl#hasDbXref	マッキューン・オルブライト症候群	McCune-Albright syndrome	https://identifiers.org/kegg.disease:H00501
NANDO:2200412	http://nanbyodata.jp/ontology/NANDO_2200412	マッキューン・オルブライト症候群	McCune-Albright syndrome	H00501	http://www.geneontology.org/formats/oboInOwl#hasDbXref	多骨性線維性骨異形成症	McCune-Albright syndrome	https://identifiers.org/kegg.disease:H00501
NANDO:2200412	http://nanbyodata.jp/ontology/NANDO_2200412	マッキューン・オルブライト症候群	McCune-Albright syndrome	H00501	http://www.geneontology.org/formats/oboInOwl#hasDbXref	アルブライト遺伝性骨ジストロフィー	McCune-Albright syndrome	https://identifiers.org/kegg.disease:H00501
NANDO:2200412	http://nanbyodata.jp/ontology/NANDO_2200412	マッキューン・オルブライト症候群	McCune-Albright syndrome	H00501	http://www.geneontology.org/formats/oboInOwl#hasDbXref	マッキューン・オルブライト症候群	Albright hereditary osteodystrophy	https://identifiers.org/kegg.disease:H00501
NANDO:2200412	http://nanbyodata.jp/ontology/NANDO_2200412	マッキューン・オルブライト症候群	McCune-Albright syndrome	H00501	http://www.geneontology.org/formats/oboInOwl#hasDbXref	多骨性線維性骨異形成症	Albright hereditary osteodystrophy	https://identifiers.org/kegg.disease:H00501
NANDO:2200412	http://nanbyodata.jp/ontology/NANDO_2200412	マッキューン・オルブライト症候群	McCune-Albright syndrome	H00501	http://www.geneontology.org/formats/oboInOwl#hasDbXref	アルブライト遺伝性骨ジストロフィー	Albright hereditary osteodystrophy	https://identifiers.org/kegg.disease:H00501
NANDO:2200412	http://nanbyodata.jp/ontology/NANDO_2200412	マッキューン・オルブライト症候群	McCune-Albright syndrome	H00501	http://www.geneontology.org/formats/oboInOwl#hasDbXref	マッキューン・オルブライト症候群	Fibrous dysplasia, polyostotic	https://identifiers.org/kegg.disease:H00501
NANDO:2200412	http://nanbyodata.jp/ontology/NANDO_2200412	マッキューン・オルブライト症候群	McCune-Albright syndrome	H00501	http://www.geneontology.org/formats/oboInOwl#hasDbXref	多骨性線維性骨異形成症	Fibrous dysplasia, polyostotic	https://identifiers.org/kegg.disease:H00501
NANDO:2200412	http://nanbyodata.jp/ontology/NANDO_2200412	マッキューン・オルブライト症候群	McCune-Albright syndrome	H00501	http://www.geneontology.org/formats/oboInOwl#hasDbXref	アルブライト遺伝性骨ジストロフィー	Fibrous dysplasia, polyostotic	https://identifiers.org/kegg.disease:H00501
NANDO:2200413	http://nanbyodata.jp/ontology/NANDO_2200413	ヌーナン症候群	Noonan syndrome	H01738	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ヌーナン症候群	Noonan syndrome	https://identifiers.org/kegg.disease:H01738
NANDO:2200414	http://nanbyodata.jp/ontology/NANDO_2200414	バルデー・ビードル症候群	Bardet-Biedl syndrome	H00418	http://www.geneontology.org/formats/oboInOwl#hasDbXref	バルデ・ビードル症候群	Bardet-Biedl syndrome	https://identifiers.org/kegg.disease:H00418
NANDO:2200415	http://nanbyodata.jp/ontology/NANDO_2200415	若年性特発性関節炎	Juvenile idiopathic arthritis	H01672	http://www.geneontology.org/formats/oboInOwl#hasDbXref	若年性特発性関節炎	Juvenile idiopathic arthritis	https://identifiers.org/kegg.disease:H01672
NANDO:2200416	http://nanbyodata.jp/ontology/NANDO_2200416	全身性エリテマトーデス	Systemic lupus erythematosus	H00080	http://www.geneontology.org/formats/oboInOwl#hasDbXref	全身性エリテマトーデス	Systemic lupus erythematosus	https://identifiers.org/kegg.disease:H00080
NANDO:2200417	http://nanbyodata.jp/ontology/NANDO_2200417	皮膚筋炎／多発性筋炎	Juvenile dermatomyositis, polymyositis	H01604	http://www.geneontology.org/formats/oboInOwl#hasDbXref	皮膚筋炎/多発性筋炎	Polymyositis and dermatomyositis	https://identifiers.org/kegg.disease:H01604
NANDO:2200420	http://nanbyodata.jp/ontology/NANDO_2200420	シェーグレン症候群	Sjogren's syndrome	H01502	http://www.geneontology.org/formats/oboInOwl#hasDbXref	シェーグレン症候群	Sjogren syndrome	https://identifiers.org/kegg.disease:H01502
NANDO:2200421	http://nanbyodata.jp/ontology/NANDO_2200421	抗リン脂質抗体症候群	Anti-phospholipid antibody syndrome	H01697	http://www.geneontology.org/formats/oboInOwl#hasDbXref	抗リン脂質抗体症候群	Antiphospholipid syndrome	https://identifiers.org/kegg.disease:H01697
NANDO:2200422	http://nanbyodata.jp/ontology/NANDO_2200422	ベーチェット病	Behcet's disease	H01476	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ベーチェット病	Behcet disease	https://identifiers.org/kegg.disease:H01476
NANDO:2200422	http://nanbyodata.jp/ontology/NANDO_2200422	ベーチェット病	Behcet's disease	H01476	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ベーチェット病	Behcet syndrome	https://identifiers.org/kegg.disease:H01476
NANDO:2200424	http://nanbyodata.jp/ontology/NANDO_2200424	多発血管炎性肉芽腫症	Granulomatosis with polyangiitis	H01655	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ウェゲナー肉芽腫症	Granulomatosis with polyangiitis	https://identifiers.org/kegg.disease:H01655
NANDO:2200424	http://nanbyodata.jp/ontology/NANDO_2200424	多発血管炎性肉芽腫症	Granulomatosis with polyangiitis	H01655	http://www.geneontology.org/formats/oboInOwl#hasDbXref	多発血管炎性肉芽腫症	Granulomatosis with polyangiitis	https://identifiers.org/kegg.disease:H01655
NANDO:2200424	http://nanbyodata.jp/ontology/NANDO_2200424	多発血管炎性肉芽腫症	Granulomatosis with polyangiitis	H01655	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ウェゲナー肉芽腫症	Wegener granulomatosis	https://identifiers.org/kegg.disease:H01655
NANDO:2200424	http://nanbyodata.jp/ontology/NANDO_2200424	多発血管炎性肉芽腫症	Granulomatosis with polyangiitis	H01655	http://www.geneontology.org/formats/oboInOwl#hasDbXref	多発血管炎性肉芽腫症	Wegener granulomatosis	https://identifiers.org/kegg.disease:H01655
NANDO:2200426	http://nanbyodata.jp/ontology/NANDO_2200426	顕微鏡的多発血管炎	Microscopic polyangiitis	H01658	http://www.geneontology.org/formats/oboInOwl#hasDbXref	顕微鏡的多発血管炎	Microscopic polyangiitis	https://identifiers.org/kegg.disease:H01658
NANDO:2200427	http://nanbyodata.jp/ontology/NANDO_2200427	好酸球性多発血管炎性肉芽腫症	Eosinophilic granulomatosis with polyangiitis	H01468	http://www.geneontology.org/formats/oboInOwl#hasDbXref	好酸球性多発血管炎性肉芽腫症	Eosinophilic granulomatosis with polyangiitis	https://identifiers.org/kegg.disease:H01468
NANDO:2200427	http://nanbyodata.jp/ontology/NANDO_2200427	好酸球性多発血管炎性肉芽腫症	Eosinophilic granulomatosis with polyangiitis	H01468	http://www.geneontology.org/formats/oboInOwl#hasDbXref	チャーグストラウス症候群	Eosinophilic granulomatosis with polyangiitis	https://identifiers.org/kegg.disease:H01468
NANDO:2200427	http://nanbyodata.jp/ontology/NANDO_2200427	好酸球性多発血管炎性肉芽腫症	Eosinophilic granulomatosis with polyangiitis	H01468	http://www.geneontology.org/formats/oboInOwl#hasDbXref	好酸球性多発血管炎性肉芽腫症	Churg-Strauss syndrome	https://identifiers.org/kegg.disease:H01468
NANDO:2200427	http://nanbyodata.jp/ontology/NANDO_2200427	好酸球性多発血管炎性肉芽腫症	Eosinophilic granulomatosis with polyangiitis	H01468	http://www.geneontology.org/formats/oboInOwl#hasDbXref	チャーグストラウス症候群	Churg-Strauss syndrome	https://identifiers.org/kegg.disease:H01468
NANDO:2200428	http://nanbyodata.jp/ontology/NANDO_2200428	再発性多発軟骨炎	Relapsing polychondritis	H01758	http://www.geneontology.org/formats/oboInOwl#hasDbXref	再発性多発軟骨炎	Relapsing polychondritis	https://identifiers.org/kegg.disease:H01758
NANDO:2200429	http://nanbyodata.jp/ontology/NANDO_2200429	全身性強皮症	Systemic sclerosis	H01492	http://www.geneontology.org/formats/oboInOwl#hasDbXref	全身性強皮症	Systemic scleroderma	https://identifiers.org/kegg.disease:H01492
NANDO:2200429	http://nanbyodata.jp/ontology/NANDO_2200429	全身性強皮症	Systemic sclerosis	H01492	http://www.geneontology.org/formats/oboInOwl#hasDbXref	全身性強皮症	Systemic sclerosis	https://identifiers.org/kegg.disease:H01492
NANDO:2200430	http://nanbyodata.jp/ontology/NANDO_2200430	混合性結合組織病	Mixed connective tissue disease	H01710	http://www.geneontology.org/formats/oboInOwl#hasDbXref	混合性結合組織病	Mixed connective tissue disease	https://identifiers.org/kegg.disease:H01710
NANDO:2200431	http://nanbyodata.jp/ontology/NANDO_2200431	家族性地中海熱	Familial Mediterranean fever	H00288	http://www.geneontology.org/formats/oboInOwl#hasDbXref	家族性地中海熱	Familial Mediterranean fever	https://identifiers.org/kegg.disease:H00288
NANDO:2200431	http://nanbyodata.jp/ontology/NANDO_2200431	家族性地中海熱	Familial Mediterranean fever	H00288	http://www.geneontology.org/formats/oboInOwl#hasDbXref	家族性地中海熱	Familial hereditary periodic fever syndromes	https://identifiers.org/kegg.disease:H00288
NANDO:2200432	http://nanbyodata.jp/ontology/NANDO_2200432	クリオピリン関連周期熱症候群	Cryopyrin-associated periodic syndrome	H00282	http://www.geneontology.org/formats/oboInOwl#hasDbXref	クリオピリン関連周期熱症候群	Cryopyrin associated periodic syndrome	https://identifiers.org/kegg.disease:H00282
NANDO:2200433	http://nanbyodata.jp/ontology/NANDO_2200433	TNF受容体関連周期性症候群	TNF receptor-associated periodic fever syndrome	H00912	http://www.geneontology.org/formats/oboInOwl#hasDbXref	TNF受容体関連周期性症候群	Familial periodic fever	https://identifiers.org/kegg.disease:H00912
NANDO:2200433	http://nanbyodata.jp/ontology/NANDO_2200433	TNF受容体関連周期性症候群	TNF receptor-associated periodic fever syndrome	H00912	http://www.geneontology.org/formats/oboInOwl#hasDbXref	TNF受容体関連周期性症候群	Tumor necrosis factor receptor-associated periodic syndrome	https://identifiers.org/kegg.disease:H00912
NANDO:2200434	http://nanbyodata.jp/ontology/NANDO_2200434	ブラウ症候群	Blau syndrome, early onset sarcoidosis	H00285	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ブラウ症候群	Blau syndrome	https://identifiers.org/kegg.disease:H00285
NANDO:2200437	http://nanbyodata.jp/ontology/NANDO_2200437	化膿性無菌性関節炎・壊疽性膿皮症・アクネ症候群	Pyogenic arthritis, pyoderma gangrenosum, acne syndrome	H00287	http://www.geneontology.org/formats/oboInOwl#hasDbXref	化膿性無菌性関節炎・壊疽性膿皮症・アクネ症候群	Pyogenic sterile arthritis, pyoderma gangrenosum, and acne syndrome	https://identifiers.org/kegg.disease:H00287
NANDO:2200438	http://nanbyodata.jp/ontology/NANDO_2200438	慢性再発性多発性骨髄炎	Chronic recurrent multifocal osteomyelitis	H01117	http://www.geneontology.org/formats/oboInOwl#hasDbXref	慢性再発性多発性骨髄炎	Chronic recurrent multifocal osteomyelitis	https://identifiers.org/kegg.disease:H01117
NANDO:2200438	http://nanbyodata.jp/ontology/NANDO_2200438	慢性再発性多発性骨髄炎	Chronic recurrent multifocal osteomyelitis	H01117	http://www.geneontology.org/formats/oboInOwl#hasDbXref	Majeed 症候群	Chronic recurrent multifocal osteomyelitis	https://identifiers.org/kegg.disease:H01117
NANDO:2200438	http://nanbyodata.jp/ontology/NANDO_2200438	慢性再発性多発性骨髄炎	Chronic recurrent multifocal osteomyelitis	H01117	http://www.geneontology.org/formats/oboInOwl#hasDbXref	慢性再発性多発性骨髄炎	Majeed syndrome	https://identifiers.org/kegg.disease:H01117
NANDO:2200438	http://nanbyodata.jp/ontology/NANDO_2200438	慢性再発性多発性骨髄炎	Chronic recurrent multifocal osteomyelitis	H01117	http://www.geneontology.org/formats/oboInOwl#hasDbXref	Majeed 症候群	Majeed syndrome	https://identifiers.org/kegg.disease:H01117
NANDO:2200442	http://nanbyodata.jp/ontology/NANDO_2200442	自己炎症合併フォスフォリパーゼCγ2関連抗体欠損免疫異常症	Autoinflammation and PLCG2-associated antibody deficiency and immune dysregulation	H01743	http://www.geneontology.org/formats/oboInOwl#hasDbXref	自己炎症合併フォスフォリパーゼＣγ2 関連抗体欠損・免疫異常症	Autoinflammation and PLCG2-associated antibody deficiency and immune dysregulation	https://identifiers.org/kegg.disease:H01743
NANDO:2200460	http://nanbyodata.jp/ontology/NANDO_2200460	1型糖尿病	Diabetes mellitus type 1	H00408	http://www.geneontology.org/formats/oboInOwl#hasDbXref	1型糖尿病	Type 1 diabetes mellitus	https://identifiers.org/kegg.disease:H00408
NANDO:2200461	http://nanbyodata.jp/ontology/NANDO_2200461	2型糖尿病	Diabetes mellitus type 2	H00409	http://www.geneontology.org/formats/oboInOwl#hasDbXref	2型糖尿病	Type 2 diabetes mellitus	https://identifiers.org/kegg.disease:H00409
NANDO:2200467	http://nanbyodata.jp/ontology/NANDO_2200467	フェニルケトン尿症	Phenylketonuria	H00167	http://www.geneontology.org/formats/oboInOwl#hasDbXref	フェニルケトン尿症	Hyperphenylalaninemia	https://identifiers.org/kegg.disease:H00167
NANDO:2200467	http://nanbyodata.jp/ontology/NANDO_2200467	フェニルケトン尿症	Phenylketonuria	H00167	http://www.geneontology.org/formats/oboInOwl#hasDbXref	高フェニルアラニン血症	Hyperphenylalaninemia	https://identifiers.org/kegg.disease:H00167
NANDO:2200467	http://nanbyodata.jp/ontology/NANDO_2200467	フェニルケトン尿症	Phenylketonuria	H00167	http://www.geneontology.org/formats/oboInOwl#hasDbXref	フェニルケトン尿症	Phenylketonuria	https://identifiers.org/kegg.disease:H00167
NANDO:2200467	http://nanbyodata.jp/ontology/NANDO_2200467	フェニルケトン尿症	Phenylketonuria	H00167	http://www.geneontology.org/formats/oboInOwl#hasDbXref	高フェニルアラニン血症	Phenylketonuria	https://identifiers.org/kegg.disease:H00167
NANDO:2200471	http://nanbyodata.jp/ontology/NANDO_2200471	高プロリン血症	Hyperprolinemia	H00190	http://www.geneontology.org/formats/oboInOwl#hasDbXref	高プロリン血症	Hyperprolinemia	https://identifiers.org/kegg.disease:H00190
NANDO:2200472	http://nanbyodata.jp/ontology/NANDO_2200472	プロリダーゼ欠損症	Prolidase deficiency	H01119	http://www.geneontology.org/formats/oboInOwl#hasDbXref	プロリダーゼ欠損症	Prolidase deficiency	https://identifiers.org/kegg.disease:H01119
NANDO:2200473	http://nanbyodata.jp/ontology/NANDO_2200473	メープルシロップ尿症	Maple syrup urine disease	H00172	http://www.geneontology.org/formats/oboInOwl#hasDbXref	メープルシロップ尿症	Maple syrup urine disease	https://identifiers.org/kegg.disease:H00172
NANDO:2200474	http://nanbyodata.jp/ontology/NANDO_2200474	ホモシスチン尿症	Homocystinuria	H00183	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ホモシスチン尿症	Homocystinuria	https://identifiers.org/kegg.disease:H00183
NANDO:2200475	http://nanbyodata.jp/ontology/NANDO_2200475	高メチオニン血症	Hypermethioninemia	H00184	http://www.geneontology.org/formats/oboInOwl#hasDbXref	高メチオニン血症	Hypermethioninemia	https://identifiers.org/kegg.disease:H00184
NANDO:2200476	http://nanbyodata.jp/ontology/NANDO_2200476	非ケトーシス型高グリシン血症	Nonketotic hyperglycinemia	H00191	http://www.geneontology.org/formats/oboInOwl#hasDbXref	非ケトーシス型高グリシン血症	Nonketotic hyperglycinemia	https://identifiers.org/kegg.disease:H00191
NANDO:2200476	http://nanbyodata.jp/ontology/NANDO_2200476	非ケトーシス型高グリシン血症	Nonketotic hyperglycinemia	H00191	http://www.geneontology.org/formats/oboInOwl#hasDbXref	グリシン脳症	Nonketotic hyperglycinemia	https://identifiers.org/kegg.disease:H00191
NANDO:2200476	http://nanbyodata.jp/ontology/NANDO_2200476	非ケトーシス型高グリシン血症	Nonketotic hyperglycinemia	H00191	http://www.geneontology.org/formats/oboInOwl#hasDbXref	非ケトーシス型高グリシン血症	Glycine encephalopathy (GCE)	https://identifiers.org/kegg.disease:H00191
NANDO:2200476	http://nanbyodata.jp/ontology/NANDO_2200476	非ケトーシス型高グリシン血症	Nonketotic hyperglycinemia	H00191	http://www.geneontology.org/formats/oboInOwl#hasDbXref	グリシン脳症	Glycine encephalopathy (GCE)	https://identifiers.org/kegg.disease:H00191
NANDO:2200477	http://nanbyodata.jp/ontology/NANDO_2200477	N-アセチルグルタミン酸合成酵素欠損症	N-acetylglutamate synthetase deficiency	H01032	http://www.geneontology.org/formats/oboInOwl#hasDbXref	NAGS欠損症	N-acetylglutamate synthase deficiency	https://identifiers.org/kegg.disease:H01032
NANDO:2200477	http://nanbyodata.jp/ontology/NANDO_2200477	N-アセチルグルタミン酸合成酵素欠損症	N-acetylglutamate synthetase deficiency	H01032	http://www.geneontology.org/formats/oboInOwl#hasDbXref	N-アセチルグルタミン酸合成酵素欠損症	N-acetylglutamate synthase deficiency	https://identifiers.org/kegg.disease:H01032
NANDO:2200479	http://nanbyodata.jp/ontology/NANDO_2200479	オルニチントランスカルバミラーゼ欠損症	Ornithine transcarbamylase deficiency	H00187	http://www.geneontology.org/formats/oboInOwl#hasDbXref	オルニチントランスカルバミラーゼ欠損症	Ornithine transcarbamylase deficiency	https://identifiers.org/kegg.disease:H00187
NANDO:2200481	http://nanbyodata.jp/ontology/NANDO_2200481	アルギニノコハク酸尿症	Argininosuccinic aciduria	H01028	http://www.geneontology.org/formats/oboInOwl#hasDbXref	アルギニノコハク酸尿症	Argininosuccinic aciduria	https://identifiers.org/kegg.disease:H01028
NANDO:2200481	http://nanbyodata.jp/ontology/NANDO_2200481	アルギニノコハク酸尿症	Argininosuccinic aciduria	H01028	http://www.geneontology.org/formats/oboInOwl#hasDbXref	アルギニノコハク酸分解酵素欠損症	Argininosuccinic aciduria	https://identifiers.org/kegg.disease:H01028
NANDO:2200481	http://nanbyodata.jp/ontology/NANDO_2200481	アルギニノコハク酸尿症	Argininosuccinic aciduria	H01028	http://www.geneontology.org/formats/oboInOwl#hasDbXref	アルギニノコハク酸尿症	Argininosuccinate lyase deficiency	https://identifiers.org/kegg.disease:H01028
NANDO:2200481	http://nanbyodata.jp/ontology/NANDO_2200481	アルギニノコハク酸尿症	Argininosuccinic aciduria	H01028	http://www.geneontology.org/formats/oboInOwl#hasDbXref	アルギニノコハク酸分解酵素欠損症	Argininosuccinate lyase deficiency	https://identifiers.org/kegg.disease:H01028
NANDO:2200482	http://nanbyodata.jp/ontology/NANDO_2200482	高アルギニン血症	Hyperargininemia	H00186	http://www.geneontology.org/formats/oboInOwl#hasDbXref	高アルギニン血症	Hyperargininemia	https://identifiers.org/kegg.disease:H00186
NANDO:2200484	http://nanbyodata.jp/ontology/NANDO_2200484	高オルニチン血症	Hyperornithinemia	H00189	http://www.geneontology.org/formats/oboInOwl#hasDbXref	高オルニチン血症	Gyrate Atrophy	https://identifiers.org/kegg.disease:H00189
NANDO:2200484	http://nanbyodata.jp/ontology/NANDO_2200484	高オルニチン血症	Hyperornithinemia	H00189	http://www.geneontology.org/formats/oboInOwl#hasDbXref	高オルニチン血症	Ornithinaemia	https://identifiers.org/kegg.disease:H00189
NANDO:2200487	http://nanbyodata.jp/ontology/NANDO_2200487	ハートナップ病	Hartnup disease	H00843	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ハートナップ病	Hartnup disorder	https://identifiers.org/kegg.disease:H00843
NANDO:2200488	http://nanbyodata.jp/ontology/NANDO_2200488	リジン尿性蛋白不耐症	Lysinuric protein intolerance	H00899	http://www.geneontology.org/formats/oboInOwl#hasDbXref	リジン尿性蛋白不耐症	Lysinuric protein intolerance	https://identifiers.org/kegg.disease:H00899
NANDO:2200489	http://nanbyodata.jp/ontology/NANDO_2200489	シスチン尿症	Cystinuria	H00901	http://www.geneontology.org/formats/oboInOwl#hasDbXref	シスチン尿症	Cystinuria	https://identifiers.org/kegg.disease:H00901
NANDO:2200491	http://nanbyodata.jp/ontology/NANDO_2200491	メチルマロン酸血症	Methylmalonic acidemia	H00174	http://www.geneontology.org/formats/oboInOwl#hasDbXref	メチルマロン酸血症	Methylmalonic acidemia	https://identifiers.org/kegg.disease:H00174
NANDO:2200491	http://nanbyodata.jp/ontology/NANDO_2200491	メチルマロン酸血症	Methylmalonic acidemia	H00174	http://www.geneontology.org/formats/oboInOwl#hasDbXref	メチルマロン酸尿症	Methylmalonic acidemia	https://identifiers.org/kegg.disease:H00174
NANDO:2200491	http://nanbyodata.jp/ontology/NANDO_2200491	メチルマロン酸血症	Methylmalonic acidemia	H00174	http://www.geneontology.org/formats/oboInOwl#hasDbXref	メチルマロン酸血症	Methylmalonic aciduria	https://identifiers.org/kegg.disease:H00174
NANDO:2200491	http://nanbyodata.jp/ontology/NANDO_2200491	メチルマロン酸血症	Methylmalonic acidemia	H00174	http://www.geneontology.org/formats/oboInOwl#hasDbXref	メチルマロン酸尿症	Methylmalonic aciduria	https://identifiers.org/kegg.disease:H00174
NANDO:2200492	http://nanbyodata.jp/ontology/NANDO_2200492	プロピオン酸血症	Propionic acidemia	H00175	http://www.geneontology.org/formats/oboInOwl#hasDbXref	プロピオン酸血症	Propionic acidemia	https://identifiers.org/kegg.disease:H00175
NANDO:2200493	http://nanbyodata.jp/ontology/NANDO_2200493	β-ケトチオラーゼ欠損症	Beta-ketothiolase deficiency	H01076	http://www.geneontology.org/formats/oboInOwl#hasDbXref	β-ケトチオラーゼ欠損症	Beta-ketothiolase deficiency	https://identifiers.org/kegg.disease:H01076
NANDO:2200493	http://nanbyodata.jp/ontology/NANDO_2200493	β-ケトチオラーゼ欠損症	Beta-ketothiolase deficiency	H01076	http://www.geneontology.org/formats/oboInOwl#hasDbXref	α-メチルアセト酢酸尿症	Beta-ketothiolase deficiency	https://identifiers.org/kegg.disease:H01076
NANDO:2200493	http://nanbyodata.jp/ontology/NANDO_2200493	β-ケトチオラーゼ欠損症	Beta-ketothiolase deficiency	H01076	http://www.geneontology.org/formats/oboInOwl#hasDbXref	β-ケトチオラーゼ欠損症	Alpha-methylacetoacetic aciduria	https://identifiers.org/kegg.disease:H01076
NANDO:2200493	http://nanbyodata.jp/ontology/NANDO_2200493	β-ケトチオラーゼ欠損症	Beta-ketothiolase deficiency	H01076	http://www.geneontology.org/formats/oboInOwl#hasDbXref	α-メチルアセト酢酸尿症	Alpha-methylacetoacetic aciduria	https://identifiers.org/kegg.disease:H01076
NANDO:2200494	http://nanbyodata.jp/ontology/NANDO_2200494	イソ吉草酸血症	Isovaleric acidemia	H00173	http://www.geneontology.org/formats/oboInOwl#hasDbXref	イソ吉草酸血症	Isovaleric acidemia	https://identifiers.org/kegg.disease:H00173
NANDO:2200496	http://nanbyodata.jp/ontology/NANDO_2200496	メチルグルタコン酸尿症	Methylglutaconic aciduria	H00754	http://www.geneontology.org/formats/oboInOwl#hasDbXref	メチルグルタコン酸尿症	3-Methylglutaconic aciduria	https://identifiers.org/kegg.disease:H00754
NANDO:2200500	http://nanbyodata.jp/ontology/NANDO_2200500	複合カルボキシラーゼ欠損症	Multiple carboxylase deficiency	H00180	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ホロカルボキシラーゼ合成酵素欠損症	Holocarboxylase synthetase deficiency	https://identifiers.org/kegg.disease:H00180
NANDO:2200500	http://nanbyodata.jp/ontology/NANDO_2200500	複合カルボキシラーゼ欠損症	Multiple carboxylase deficiency	H00180	http://www.geneontology.org/formats/oboInOwl#hasDbXref	複合カルボキシラーゼ欠損症	Holocarboxylase synthetase deficiency	https://identifiers.org/kegg.disease:H00180
NANDO:2200500	http://nanbyodata.jp/ontology/NANDO_2200500	複合カルボキシラーゼ欠損症	Multiple carboxylase deficiency	H00180	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ホロカルボキシラーゼ合成酵素欠損症	Multiple carboxylase deficiency	https://identifiers.org/kegg.disease:H00180
NANDO:2200500	http://nanbyodata.jp/ontology/NANDO_2200500	複合カルボキシラーゼ欠損症	Multiple carboxylase deficiency	H00180	http://www.geneontology.org/formats/oboInOwl#hasDbXref	複合カルボキシラーゼ欠損症	Multiple carboxylase deficiency	https://identifiers.org/kegg.disease:H00180
NANDO:2200503	http://nanbyodata.jp/ontology/NANDO_2200503	原発性高シュウ酸尿症	Primary hyperoxaluria	H00117	http://www.geneontology.org/formats/oboInOwl#hasDbXref	原発性高シュウ酸尿症	Primary hyperoxaluria	https://identifiers.org/kegg.disease:H00117
NANDO:1200901	http://nanbyodata.jp/ontology/NANDO_1200901	クロンカイト・カナダ症候群	Cronkhite-Canada syndrome	H01874	http://www.geneontology.org/formats/oboInOwl#hasDbXref	クロンカイト・カナダ症候群	Cronkhite-Canada syndrome	https://identifiers.org/kegg.disease:H01874
NANDO:1200949	http://nanbyodata.jp/ontology/NANDO_1200949	進行性白質脳症	Progressive leukoencephalopathy	H02598	http://www.geneontology.org/formats/oboInOwl#hasDbXref	進行性白質脳症	Progressive leukoencephalopathy	https://identifiers.org/kegg.disease:H02598
NANDO:1200952	http://nanbyodata.jp/ontology/NANDO_1200952	卵巣機能障害を伴う進行性白質脳症	Leukoencephalopathy, progressive, with ovarian failure	H02200	http://www.geneontology.org/formats/oboInOwl#hasDbXref	卵巣機能障害を伴う進行性白質脳症	Leukoencephalopathy, progressive, with ovarian failure	https://identifiers.org/kegg.disease:H02200
NANDO:1200952	http://nanbyodata.jp/ontology/NANDO_1200952	卵巣機能障害を伴う進行性白質脳症	Leukoencephalopathy, progressive, with ovarian failure	H02200	http://www.geneontology.org/formats/oboInOwl#hasDbXref	卵巣白質ジストロフィー	Leukoencephalopathy, progressive, with ovarian failure	https://identifiers.org/kegg.disease:H02200
NANDO:1200952	http://nanbyodata.jp/ontology/NANDO_1200952	卵巣機能障害を伴う進行性白質脳症	Leukoencephalopathy, progressive, with ovarian failure	H02200	http://www.geneontology.org/formats/oboInOwl#hasDbXref	卵巣機能障害を伴う進行性白質脳症	Ovarioleukodystrophy	https://identifiers.org/kegg.disease:H02200
NANDO:1200952	http://nanbyodata.jp/ontology/NANDO_1200952	卵巣機能障害を伴う進行性白質脳症	Leukoencephalopathy, progressive, with ovarian failure	H02200	http://www.geneontology.org/formats/oboInOwl#hasDbXref	卵巣白質ジストロフィー	Ovarioleukodystrophy	https://identifiers.org/kegg.disease:H02200
NANDO:1200954	http://nanbyodata.jp/ontology/NANDO_1200954	ウンフェルリヒト・ルントボルグ病	Unverricht-Lundborg disease	H01995	http://www.geneontology.org/formats/oboInOwl#hasDbXref	Unverricht-Lundborg 病	Unverricht-Lundborg disease	https://identifiers.org/kegg.disease:H01995
NANDO:1200954	http://nanbyodata.jp/ontology/NANDO_1200954	ウンフェルリヒト・ルントボルグ病	Unverricht-Lundborg disease	H01995	http://www.geneontology.org/formats/oboInOwl#hasDbXref	進行性ミオクローヌスてんかん 1 型	Unverricht-Lundborg disease	https://identifiers.org/kegg.disease:H01995
NANDO:1200954	http://nanbyodata.jp/ontology/NANDO_1200954	ウンフェルリヒト・ルントボルグ病	Unverricht-Lundborg disease	H01995	http://www.geneontology.org/formats/oboInOwl#hasDbXref	Unverricht-Lundborg 病	Epilepsy, progressive myoclonic 1	https://identifiers.org/kegg.disease:H01995
NANDO:1200954	http://nanbyodata.jp/ontology/NANDO_1200954	ウンフェルリヒト・ルントボルグ病	Unverricht-Lundborg disease	H01995	http://www.geneontology.org/formats/oboInOwl#hasDbXref	進行性ミオクローヌスてんかん 1 型	Epilepsy, progressive myoclonic 1	https://identifiers.org/kegg.disease:H01995
NANDO:1200955	http://nanbyodata.jp/ontology/NANDO_1200955	ラフォラ病	Lafora disease	H01994	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ラフォラ病	Lafora disease	https://identifiers.org/kegg.disease:H01994
NANDO:1200956	http://nanbyodata.jp/ontology/NANDO_1200956	良性成人型家族性ミオクローヌスてんかん	Benign adult familial myoclonus epilepsy	H02213	http://www.geneontology.org/formats/oboInOwl#hasDbXref	良性成人型家族性ミオクローヌスてんかん	Familial adult myoclonic epilepsy	https://identifiers.org/kegg.disease:H02213
NANDO:1200956	http://nanbyodata.jp/ontology/NANDO_1200956	良性成人型家族性ミオクローヌスてんかん	Benign adult familial myoclonus epilepsy	H02213	http://www.geneontology.org/formats/oboInOwl#hasDbXref	良性成人型家族性ミオクローヌスてんかん	Benign adult familial myoclonic epilepsy	https://identifiers.org/kegg.disease:H02213
NANDO:1200962	http://nanbyodata.jp/ontology/NANDO_1200962	先天性三尖弁狭窄症	Congenital tricuspid stenosis	H02602	http://www.geneontology.org/formats/oboInOwl#hasDbXref	先天性三尖弁狭窄症	Congenital tricuspid valve stenosis	https://identifiers.org/kegg.disease:H02602
NANDO:1200964	http://nanbyodata.jp/ontology/NANDO_1200964	先天性肺静脈狭窄症	Congenital pulmonary vein stenosis	H02605	http://www.geneontology.org/formats/oboInOwl#hasDbXref	先天性肺静脈狭窄症	Congenital pulmonary venous stenosis	https://identifiers.org/kegg.disease:H02605
NANDO:1200965	http://nanbyodata.jp/ontology/NANDO_1200965	左肺動脈右肺動脈起始症	Vascular sling	H02601	http://www.geneontology.org/formats/oboInOwl#hasDbXref	左肺動脈右肺動脈起始症	Vascular sling	https://identifiers.org/kegg.disease:H02601
NANDO:1200965	http://nanbyodata.jp/ontology/NANDO_1200965	左肺動脈右肺動脈起始症	Vascular sling	H02601	http://www.geneontology.org/formats/oboInOwl#hasDbXref	肺動脈スリング	Vascular sling	https://identifiers.org/kegg.disease:H02601
NANDO:1200965	http://nanbyodata.jp/ontology/NANDO_1200965	左肺動脈右肺動脈起始症	Vascular sling	H02601	http://www.geneontology.org/formats/oboInOwl#hasDbXref	左肺動脈右肺動脈起始症	Pulmonary arterial sling	https://identifiers.org/kegg.disease:H02601
NANDO:1200965	http://nanbyodata.jp/ontology/NANDO_1200965	左肺動脈右肺動脈起始症	Vascular sling	H02601	http://www.geneontology.org/formats/oboInOwl#hasDbXref	肺動脈スリング	Pulmonary arterial sling	https://identifiers.org/kegg.disease:H02601
NANDO:1200969	http://nanbyodata.jp/ontology/NANDO_1200969	カルニチン回路異常症	Carnitine cycle disorders	H02596	http://www.geneontology.org/formats/oboInOwl#hasDbXref	カルニチン回路異常症	Disorders of carnitine transport and the carnitine cycle	https://identifiers.org/kegg.disease:H02596
NANDO:1200970	http://nanbyodata.jp/ontology/NANDO_1200970	カルニチンパルミトイルトランスフェラーゼI欠損症	Carnitine palmitoyltransferase I deficiency	H01981	http://www.geneontology.org/formats/oboInOwl#hasDbXref	カルニチンパルミトイルトランスフェラーゼ I 欠損症	Carnitine palmitoyltransferase I deficiency	https://identifiers.org/kegg.disease:H01981
NANDO:1200971	http://nanbyodata.jp/ontology/NANDO_1200971	カルニチンパルミトイルトランスフェラーゼII欠損症	Carnitine palmitoyltransferase II deficiency	H01982	http://www.geneontology.org/formats/oboInOwl#hasDbXref	カルニチンパルミトイルトランスフェラーゼ II 欠損症	Carnitine palmitoyltransferase II deficiency	https://identifiers.org/kegg.disease:H01982
NANDO:1200972	http://nanbyodata.jp/ontology/NANDO_1200972	カルニチン/アシルカルニチントランスロカーゼ欠損症	Carnitine-acylcarnitine translocase deficiency	H01983	http://www.geneontology.org/formats/oboInOwl#hasDbXref	カルニチン-アシルカルニチントランスロカーゼ欠損症	Carnitine-acylcarnitine translocase deficiency	https://identifiers.org/kegg.disease:H01983
NANDO:1200982	http://nanbyodata.jp/ontology/NANDO_1200982	セピアプテリン還元酵素欠損症	Sepiapterin reductase deficiency	H02597	http://www.geneontology.org/formats/oboInOwl#hasDbXref	セピアプテリン還元酵素 (SR) 欠損症	Sepiapterin reductase deficiency	https://identifiers.org/kegg.disease:H02597
NANDO:1200993	http://nanbyodata.jp/ontology/NANDO_1200993	遺伝性自己炎症疾患	Hereditary autoinflammatory syndrome	H02599	http://www.geneontology.org/formats/oboInOwl#hasDbXref	遺伝性自己炎症疾患	Inherited autoinflammatory disease	https://identifiers.org/kegg.disease:H02599
NANDO:1201003	http://nanbyodata.jp/ontology/NANDO_1201003	先天性気管狭窄症	Congenital tracheal stenosis	H02600	http://www.geneontology.org/formats/oboInOwl#hasDbXref	先天性気管狭窄症	Congenital tracheal stenosis	https://identifiers.org/kegg.disease:H02600
NANDO:1201059	http://nanbyodata.jp/ontology/NANDO_1201059	バレー・ジェロルド症候群	Baller-Gerold syndrome	H01993	http://www.geneontology.org/formats/oboInOwl#hasDbXref	バラー・ゲロルト症候群	Baller-Gerold syndrome	https://identifiers.org/kegg.disease:H01993
NANDO:1201087	http://nanbyodata.jp/ontology/NANDO_1201087	脆弱角膜症候群	Brittle cornea syndrome	H01902	http://www.geneontology.org/formats/oboInOwl#hasDbXref	脆弱角膜症候群	Brittle cornea syndrome	https://identifiers.org/kegg.disease:H01902
NANDO:1201099	http://nanbyodata.jp/ontology/NANDO_1201099	変容性骨異形成症	Metatropic dysplasia	H02184	http://www.geneontology.org/formats/oboInOwl#hasDbXref	変容性骨異形成症	Metatropic dysplasia	https://identifiers.org/kegg.disease:H02184
NANDO:1201103	http://nanbyodata.jp/ontology/NANDO_1201103	短指を伴う家族性指関節症	Familial digital arthropathy with brachydactyly	H02062	http://www.geneontology.org/formats/oboInOwl#hasDbXref	短指を伴う家族性指関節症	Familial digital arthropathy-brachydactyly	https://identifiers.org/kegg.disease:H02062
NANDO:2100014	http://nanbyodata.jp/ontology/NANDO_2100014	家族性若年性高尿酸血症性腎症	Familial juvenile hyperuricemic nephropathy	H02011	http://www.geneontology.org/formats/oboInOwl#hasDbXref	家族性若年性高尿酸血症性腎症	Familial juvenile hyperuricemic nephropathy	https://identifiers.org/kegg.disease:H02011
NANDO:2100019	http://nanbyodata.jp/ontology/NANDO_2100019	尿細管性アシドーシス	Renal tubular acidosis	H02310	http://www.geneontology.org/formats/oboInOwl#hasDbXref	尿細管性アシドーシス	Renal tubular acidosis	https://identifiers.org/kegg.disease:H02310
NANDO:2100039	http://nanbyodata.jp/ontology/NANDO_2100039	閉塞性細気管支炎	Bronchiolitis obliterans	H01873	http://www.geneontology.org/formats/oboInOwl#hasDbXref	閉塞性細気管支炎	Obliterative bronchiolitis	https://identifiers.org/kegg.disease:H01873
NANDO:2100087	http://nanbyodata.jp/ontology/NANDO_2100087	心室中隔欠損症	Ventricular septal defect	H01926	http://www.geneontology.org/formats/oboInOwl#hasDbXref	心室中隔欠損症	Ventricular septal defect	https://identifiers.org/kegg.disease:H01926
NANDO:2100114	http://nanbyodata.jp/ontology/NANDO_2100114	成長ホルモン不応性症候群	Growth hormone insensitivity	H02037	http://www.geneontology.org/formats/oboInOwl#hasDbXref	成長ホルモン不応性症候群	Growth hormone insensitivity syndrome	https://identifiers.org/kegg.disease:H02037
NANDO:2100114	http://nanbyodata.jp/ontology/NANDO_2100114	成長ホルモン不応性症候群	Growth hormone insensitivity	H02037	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ラロン症候群	Growth hormone insensitivity syndrome	https://identifiers.org/kegg.disease:H02037
NANDO:2100114	http://nanbyodata.jp/ontology/NANDO_2100114	成長ホルモン不応性症候群	Growth hormone insensitivity	H02037	http://www.geneontology.org/formats/oboInOwl#hasDbXref	下垂体性低身長症 II型	Growth hormone insensitivity syndrome	https://identifiers.org/kegg.disease:H02037
NANDO:2100114	http://nanbyodata.jp/ontology/NANDO_2100114	成長ホルモン不応性症候群	Growth hormone insensitivity	H02037	http://www.geneontology.org/formats/oboInOwl#hasDbXref	成長ホルモン不応性症候群	Laron syndrome	https://identifiers.org/kegg.disease:H02037
NANDO:2100114	http://nanbyodata.jp/ontology/NANDO_2100114	成長ホルモン不応性症候群	Growth hormone insensitivity	H02037	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ラロン症候群	Laron syndrome	https://identifiers.org/kegg.disease:H02037
NANDO:2100114	http://nanbyodata.jp/ontology/NANDO_2100114	成長ホルモン不応性症候群	Growth hormone insensitivity	H02037	http://www.geneontology.org/formats/oboInOwl#hasDbXref	下垂体性低身長症 II型	Laron syndrome	https://identifiers.org/kegg.disease:H02037
NANDO:2100114	http://nanbyodata.jp/ontology/NANDO_2100114	成長ホルモン不応性症候群	Growth hormone insensitivity	H02037	http://www.geneontology.org/formats/oboInOwl#hasDbXref	成長ホルモン不応性症候群	Pituitary dwarfism II	https://identifiers.org/kegg.disease:H02037
NANDO:2100114	http://nanbyodata.jp/ontology/NANDO_2100114	成長ホルモン不応性症候群	Growth hormone insensitivity	H02037	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ラロン症候群	Pituitary dwarfism II	https://identifiers.org/kegg.disease:H02037
NANDO:2100114	http://nanbyodata.jp/ontology/NANDO_2100114	成長ホルモン不応性症候群	Growth hormone insensitivity	H02037	http://www.geneontology.org/formats/oboInOwl#hasDbXref	下垂体性低身長症 II型	Pituitary dwarfism II	https://identifiers.org/kegg.disease:H02037
NANDO:2100193	http://nanbyodata.jp/ontology/NANDO_2100193	メイ・ヘグリン異常症	May-Hegglin anomaly	H02051	http://www.geneontology.org/formats/oboInOwl#hasDbXref	メイ・ヘグリン異常	May-Hegglin anomaly	https://identifiers.org/kegg.disease:H02051
NANDO:2100272	http://nanbyodata.jp/ontology/NANDO_2100272	クリグラー・ナジャー症候群	Crigler-Najjar syndrome	H02054	http://www.geneontology.org/formats/oboInOwl#hasDbXref	クリグラー・ナジャー症候群	Crigler-Najjar syndrome	https://identifiers.org/kegg.disease:H02054
NANDO:2200007	http://nanbyodata.jp/ontology/NANDO_2200007	急性前骨髄球性白血病	Acute promyelocytic leukemia	H02542	http://www.geneontology.org/formats/oboInOwl#hasDbXref	急性前骨髄球性白血病	Acute promyelocytic leukemia	https://identifiers.org/kegg.disease:H02542
NANDO:2200014	http://nanbyodata.jp/ontology/NANDO_2200014	慢性骨髄単球性白血病	Chronic myelomonocytic leukemia	H02411	http://www.geneontology.org/formats/oboInOwl#hasDbXref	慢性骨髄単球性白血病	Chronic myelomonocytic leukemia	https://identifiers.org/kegg.disease:H02411
NANDO:2200015	http://nanbyodata.jp/ontology/NANDO_2200015	若年性骨髄単球性白血病	Juvenile myelomonocytic leukemia	H02541	http://www.geneontology.org/formats/oboInOwl#hasDbXref	若年性骨髄単球性白血病	Juvenile myelomonocytic leukemia	https://identifiers.org/kegg.disease:H02541
NANDO:2200038	http://nanbyodata.jp/ontology/NANDO_2200038	エルドハイム・チェスター病	Erdheim-Chester disease	H02425	http://www.geneontology.org/formats/oboInOwl#hasDbXref	エルドハイム・チェスター病	Erdheim-Chester disease	https://identifiers.org/kegg.disease:H02425
NANDO:2200046	http://nanbyodata.jp/ontology/NANDO_2200046	肝芽腫	Hepatoblastoma	H02302	http://www.geneontology.org/formats/oboInOwl#hasDbXref	肝芽腫	Hepatoblastoma	https://identifiers.org/kegg.disease:H02302
NANDO:2200139	http://nanbyodata.jp/ontology/NANDO_2200139	家族性若年性高尿酸血症性腎症	Familial juvenile hyperuricemic nephropathy	H02011	http://www.geneontology.org/formats/oboInOwl#hasDbXref	家族性若年性高尿酸血症性腎症	Familial juvenile hyperuricemic nephropathy	https://identifiers.org/kegg.disease:H02011
NANDO:2200144	http://nanbyodata.jp/ontology/NANDO_2200144	尿細管性アシドーシス	Renal tubular acidosis	H02310	http://www.geneontology.org/formats/oboInOwl#hasDbXref	尿細管性アシドーシス	Renal tubular acidosis	https://identifiers.org/kegg.disease:H02310
NANDO:2200185	http://nanbyodata.jp/ontology/NANDO_2200185	Prune belly症候群	Prune belly syndrome	H02129	http://www.geneontology.org/formats/oboInOwl#hasDbXref	Prune belly 症候群	Prune belly syndrome	https://identifiers.org/kegg.disease:H02129
NANDO:2200185	http://nanbyodata.jp/ontology/NANDO_2200185	Prune belly症候群	Prune belly syndrome	H02129	http://www.geneontology.org/formats/oboInOwl#hasDbXref	Prune belly 症候群	Eagle-Barret syndrome	https://identifiers.org/kegg.disease:H02129
NANDO:2200185	http://nanbyodata.jp/ontology/NANDO_2200185	Prune belly症候群	Prune belly syndrome	H02129	http://www.geneontology.org/formats/oboInOwl#hasDbXref	Prune belly 症候群	Triad syndrome	https://identifiers.org/kegg.disease:H02129
NANDO:2200185	http://nanbyodata.jp/ontology/NANDO_2200185	Prune belly症候群	Prune belly syndrome	H02129	http://www.geneontology.org/formats/oboInOwl#hasDbXref	Prune belly 症候群	Abdominal musculature deficiency syndrome	https://identifiers.org/kegg.disease:H02129
NANDO:2200209	http://nanbyodata.jp/ontology/NANDO_2200209	閉塞性細気管支炎	Bronchiolitis obliterans	H01873	http://www.geneontology.org/formats/oboInOwl#hasDbXref	閉塞性細気管支炎	Bronchiolitis obliterans	https://identifiers.org/kegg.disease:H01873
NANDO:2200209	http://nanbyodata.jp/ontology/NANDO_2200209	閉塞性細気管支炎	Bronchiolitis obliterans	H01873	http://www.geneontology.org/formats/oboInOwl#hasDbXref	閉塞性細気管支炎	Obliterative bronchiolitis	https://identifiers.org/kegg.disease:H01873
NANDO:2200270	http://nanbyodata.jp/ontology/NANDO_2200270	心室中隔欠損症	Ventricular septal defect	H01926	http://www.geneontology.org/formats/oboInOwl#hasDbXref	心室中隔欠損症	Ventricular septal defect	https://identifiers.org/kegg.disease:H01926
NANDO:2200291	http://nanbyodata.jp/ontology/NANDO_2200291	左肺動脈右肺動脈起始症	Vascular sling	H02601	http://www.geneontology.org/formats/oboInOwl#hasDbXref	左肺動脈右肺動脈起始症	Vascular sling	https://identifiers.org/kegg.disease:H02601
NANDO:2200291	http://nanbyodata.jp/ontology/NANDO_2200291	左肺動脈右肺動脈起始症	Vascular sling	H02601	http://www.geneontology.org/formats/oboInOwl#hasDbXref	肺動脈スリング	Vascular sling	https://identifiers.org/kegg.disease:H02601
NANDO:2200291	http://nanbyodata.jp/ontology/NANDO_2200291	左肺動脈右肺動脈起始症	Vascular sling	H02601	http://www.geneontology.org/formats/oboInOwl#hasDbXref	左肺動脈右肺動脈起始症	Pulmonary arterial sling	https://identifiers.org/kegg.disease:H02601
NANDO:2200291	http://nanbyodata.jp/ontology/NANDO_2200291	左肺動脈右肺動脈起始症	Vascular sling	H02601	http://www.geneontology.org/formats/oboInOwl#hasDbXref	肺動脈スリング	Pulmonary arterial sling	https://identifiers.org/kegg.disease:H02601
NANDO:2200321	http://nanbyodata.jp/ontology/NANDO_2200321	成長ホルモン不応性症候群	Growth hormone insensitivity	H02037	http://www.geneontology.org/formats/oboInOwl#hasDbXref	成長ホルモン不応性症候群	Growth hormone insensitivity syndrome	https://identifiers.org/kegg.disease:H02037
NANDO:2200321	http://nanbyodata.jp/ontology/NANDO_2200321	成長ホルモン不応性症候群	Growth hormone insensitivity	H02037	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ラロン症候群	Growth hormone insensitivity syndrome	https://identifiers.org/kegg.disease:H02037
NANDO:2200321	http://nanbyodata.jp/ontology/NANDO_2200321	成長ホルモン不応性症候群	Growth hormone insensitivity	H02037	http://www.geneontology.org/formats/oboInOwl#hasDbXref	下垂体性低身長症 II型	Growth hormone insensitivity syndrome	https://identifiers.org/kegg.disease:H02037
NANDO:2200321	http://nanbyodata.jp/ontology/NANDO_2200321	成長ホルモン不応性症候群	Growth hormone insensitivity	H02037	http://www.geneontology.org/formats/oboInOwl#hasDbXref	成長ホルモン不応性症候群	Laron syndrome	https://identifiers.org/kegg.disease:H02037
NANDO:2200321	http://nanbyodata.jp/ontology/NANDO_2200321	成長ホルモン不応性症候群	Growth hormone insensitivity	H02037	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ラロン症候群	Laron syndrome	https://identifiers.org/kegg.disease:H02037
NANDO:2200321	http://nanbyodata.jp/ontology/NANDO_2200321	成長ホルモン不応性症候群	Growth hormone insensitivity	H02037	http://www.geneontology.org/formats/oboInOwl#hasDbXref	下垂体性低身長症 II型	Laron syndrome	https://identifiers.org/kegg.disease:H02037
NANDO:2200321	http://nanbyodata.jp/ontology/NANDO_2200321	成長ホルモン不応性症候群	Growth hormone insensitivity	H02037	http://www.geneontology.org/formats/oboInOwl#hasDbXref	成長ホルモン不応性症候群	Pituitary dwarfism II	https://identifiers.org/kegg.disease:H02037
NANDO:2200321	http://nanbyodata.jp/ontology/NANDO_2200321	成長ホルモン不応性症候群	Growth hormone insensitivity	H02037	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ラロン症候群	Pituitary dwarfism II	https://identifiers.org/kegg.disease:H02037
NANDO:2200321	http://nanbyodata.jp/ontology/NANDO_2200321	成長ホルモン不応性症候群	Growth hormone insensitivity	H02037	http://www.geneontology.org/formats/oboInOwl#hasDbXref	下垂体性低身長症 II型	Pituitary dwarfism II	https://identifiers.org/kegg.disease:H02037
NANDO:2200378	http://nanbyodata.jp/ontology/NANDO_2200378	ゴナドトロピン非依存性思春期早発症	Non-gonadotropin-dependent precocious puberty	H02019	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ゴナドトロピン非依存性思春期早発症	Familial male-limited precocious puberty	https://identifiers.org/kegg.disease:H02019
NANDO:2200378	http://nanbyodata.jp/ontology/NANDO_2200378	ゴナドトロピン非依存性思春期早発症	Non-gonadotropin-dependent precocious puberty	H02019	http://www.geneontology.org/formats/oboInOwl#hasDbXref	家族性男性思春期早発症	Familial male-limited precocious puberty	https://identifiers.org/kegg.disease:H02019
NANDO:2200378	http://nanbyodata.jp/ontology/NANDO_2200378	ゴナドトロピン非依存性思春期早発症	Non-gonadotropin-dependent precocious puberty	H02019	http://www.geneontology.org/formats/oboInOwl#hasDbXref	家族性精巣中毒症	Familial male-limited precocious puberty	https://identifiers.org/kegg.disease:H02019
NANDO:2200378	http://nanbyodata.jp/ontology/NANDO_2200378	ゴナドトロピン非依存性思春期早発症	Non-gonadotropin-dependent precocious puberty	H02019	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ゴナドトロピン非依存性思春期早発症	Familial testotoxicosis	https://identifiers.org/kegg.disease:H02019
NANDO:2200378	http://nanbyodata.jp/ontology/NANDO_2200378	ゴナドトロピン非依存性思春期早発症	Non-gonadotropin-dependent precocious puberty	H02019	http://www.geneontology.org/formats/oboInOwl#hasDbXref	家族性男性思春期早発症	Familial testotoxicosis	https://identifiers.org/kegg.disease:H02019
NANDO:2200378	http://nanbyodata.jp/ontology/NANDO_2200378	ゴナドトロピン非依存性思春期早発症	Non-gonadotropin-dependent precocious puberty	H02019	http://www.geneontology.org/formats/oboInOwl#hasDbXref	家族性精巣中毒症	Familial testotoxicosis	https://identifiers.org/kegg.disease:H02019
NANDO:2200378	http://nanbyodata.jp/ontology/NANDO_2200378	ゴナドトロピン非依存性思春期早発症	Non-gonadotropin-dependent precocious puberty	H02019	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ゴナドトロピン非依存性思春期早発症	Gonadotropin-independent familial sexual precocity	https://identifiers.org/kegg.disease:H02019
NANDO:2200378	http://nanbyodata.jp/ontology/NANDO_2200378	ゴナドトロピン非依存性思春期早発症	Non-gonadotropin-dependent precocious puberty	H02019	http://www.geneontology.org/formats/oboInOwl#hasDbXref	家族性男性思春期早発症	Gonadotropin-independent familial sexual precocity	https://identifiers.org/kegg.disease:H02019
NANDO:2200378	http://nanbyodata.jp/ontology/NANDO_2200378	ゴナドトロピン非依存性思春期早発症	Non-gonadotropin-dependent precocious puberty	H02019	http://www.geneontology.org/formats/oboInOwl#hasDbXref	家族性精巣中毒症	Gonadotropin-independent familial sexual precocity	https://identifiers.org/kegg.disease:H02019
NANDO:2200391	http://nanbyodata.jp/ontology/NANDO_2200391	アンドロゲン不応症	Androgen insensitivity syndrome	H02177	http://www.geneontology.org/formats/oboInOwl#hasDbXref	アンドロゲン不応症	Androgen insensitivity syndrome	https://identifiers.org/kegg.disease:H02177
NANDO:2200504	http://nanbyodata.jp/ontology/NANDO_2200504	アルカプトン尿症	Alkaptonuria	H00163	http://www.geneontology.org/formats/oboInOwl#hasDbXref	アルカプトン尿症	Alkaptonuria	https://identifiers.org/kegg.disease:H00163
NANDO:2200506	http://nanbyodata.jp/ontology/NANDO_2200506	先天性胆汁酸代謝異常症	Inborn errors of bile acid metabolism	H00628	http://www.geneontology.org/formats/oboInOwl#hasDbXref	先天性胆汁酸代謝異常症	Congenital bile acid synthesis defect	https://identifiers.org/kegg.disease:H00628
NANDO:2200513	http://nanbyodata.jp/ontology/NANDO_2200513	中鎖アシルCoA脱水素酵素欠損症	Medium-chain acyl-CoA dehydrogenase deficiency	H00488	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ACADM 欠損症	MCAD deficiency	https://identifiers.org/kegg.disease:H00488
NANDO:2200513	http://nanbyodata.jp/ontology/NANDO_2200513	中鎖アシルCoA脱水素酵素欠損症	Medium-chain acyl-CoA dehydrogenase deficiency	H00488	http://www.geneontology.org/formats/oboInOwl#hasDbXref	MCAD 欠損症	MCAD deficiency	https://identifiers.org/kegg.disease:H00488
NANDO:2200513	http://nanbyodata.jp/ontology/NANDO_2200513	中鎖アシルCoA脱水素酵素欠損症	Medium-chain acyl-CoA dehydrogenase deficiency	H00488	http://www.geneontology.org/formats/oboInOwl#hasDbXref	中鎖アシル CoA デヒドロゲナーゼ欠損症	MCAD deficiency	https://identifiers.org/kegg.disease:H00488
NANDO:2200513	http://nanbyodata.jp/ontology/NANDO_2200513	中鎖アシルCoA脱水素酵素欠損症	Medium-chain acyl-CoA dehydrogenase deficiency	H00488	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ACADM 欠損症	Medium-chain acyl-CoA dehydrogenase deficiency	https://identifiers.org/kegg.disease:H00488
NANDO:2200513	http://nanbyodata.jp/ontology/NANDO_2200513	中鎖アシルCoA脱水素酵素欠損症	Medium-chain acyl-CoA dehydrogenase deficiency	H00488	http://www.geneontology.org/formats/oboInOwl#hasDbXref	MCAD 欠損症	Medium-chain acyl-CoA dehydrogenase deficiency	https://identifiers.org/kegg.disease:H00488
NANDO:2200513	http://nanbyodata.jp/ontology/NANDO_2200513	中鎖アシルCoA脱水素酵素欠損症	Medium-chain acyl-CoA dehydrogenase deficiency	H00488	http://www.geneontology.org/formats/oboInOwl#hasDbXref	中鎖アシル CoA デヒドロゲナーゼ欠損症	Medium-chain acyl-CoA dehydrogenase deficiency	https://identifiers.org/kegg.disease:H00488
NANDO:2200513	http://nanbyodata.jp/ontology/NANDO_2200513	中鎖アシルCoA脱水素酵素欠損症	Medium-chain acyl-CoA dehydrogenase deficiency	H00488	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ACADM 欠損症	ACADM deficiency	https://identifiers.org/kegg.disease:H00488
NANDO:2200513	http://nanbyodata.jp/ontology/NANDO_2200513	中鎖アシルCoA脱水素酵素欠損症	Medium-chain acyl-CoA dehydrogenase deficiency	H00488	http://www.geneontology.org/formats/oboInOwl#hasDbXref	MCAD 欠損症	ACADM deficiency	https://identifiers.org/kegg.disease:H00488
NANDO:2200513	http://nanbyodata.jp/ontology/NANDO_2200513	中鎖アシルCoA脱水素酵素欠損症	Medium-chain acyl-CoA dehydrogenase deficiency	H00488	http://www.geneontology.org/formats/oboInOwl#hasDbXref	中鎖アシル CoA デヒドロゲナーゼ欠損症	ACADM deficiency	https://identifiers.org/kegg.disease:H00488
NANDO:2200515	http://nanbyodata.jp/ontology/NANDO_2200515	三頭酵素欠損症	Trifunctional protein deficiency	H01352	http://www.geneontology.org/formats/oboInOwl#hasDbXref	三頭酵素欠損症	Mitochondrial trifunctional protein deficiency	https://identifiers.org/kegg.disease:H01352
NANDO:2200518	http://nanbyodata.jp/ontology/NANDO_2200518	ピルビン酸脱水素酵素複合体欠損症	Pyruvate dehydrogenase complex deficiency	H00072	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ピルビン酸脱水素酵素複合体欠損症	Pyruvate dehydrogenase complex deficiency	https://identifiers.org/kegg.disease:H00072
NANDO:2200519	http://nanbyodata.jp/ontology/NANDO_2200519	ピルビン酸カルボキシラーゼ欠損症	Pyruvate carboxylase deficiency	H00073	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ピルビン酸カルボキシラーゼ欠損症	Pyruvate carboxylase deficiency	https://identifiers.org/kegg.disease:H00073
NANDO:2200523	http://nanbyodata.jp/ontology/NANDO_2200523	ミトコンドリアDNA枯渇症候群	Mitochondrial DNA depletion syndrome	H00469	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ミトコンドリア DNA 枯渇症候群	Mitochondrial DNA depletion syndrome	https://identifiers.org/kegg.disease:H00469
NANDO:2200526	http://nanbyodata.jp/ontology/NANDO_2200526	赤色ぼろ線維・ミオクローヌスてんかん症候群	Myoclonus epilepsy associated with ragged-red fibers	H01356	http://www.geneontology.org/formats/oboInOwl#hasDbXref	赤色ぼろ線維・ミオクローヌスてんかん症候群	Fukuhara syndrome	https://identifiers.org/kegg.disease:H01356
NANDO:2200526	http://nanbyodata.jp/ontology/NANDO_2200526	赤色ぼろ線維・ミオクローヌスてんかん症候群	Myoclonus epilepsy associated with ragged-red fibers	H01356	http://www.geneontology.org/formats/oboInOwl#hasDbXref	MERRF 症候群	Fukuhara syndrome	https://identifiers.org/kegg.disease:H01356
NANDO:2200526	http://nanbyodata.jp/ontology/NANDO_2200526	赤色ぼろ線維・ミオクローヌスてんかん症候群	Myoclonus epilepsy associated with ragged-red fibers	H01356	http://www.geneontology.org/formats/oboInOwl#hasDbXref	福原病	Fukuhara syndrome	https://identifiers.org/kegg.disease:H01356
NANDO:2200526	http://nanbyodata.jp/ontology/NANDO_2200526	赤色ぼろ線維・ミオクローヌスてんかん症候群	Myoclonus epilepsy associated with ragged-red fibers	H01356	http://www.geneontology.org/formats/oboInOwl#hasDbXref	赤色ぼろ線維・ミオクローヌスてんかん症候群	MERRF syndrome	https://identifiers.org/kegg.disease:H01356
NANDO:2200526	http://nanbyodata.jp/ontology/NANDO_2200526	赤色ぼろ線維・ミオクローヌスてんかん症候群	Myoclonus epilepsy associated with ragged-red fibers	H01356	http://www.geneontology.org/formats/oboInOwl#hasDbXref	MERRF 症候群	MERRF syndrome	https://identifiers.org/kegg.disease:H01356
NANDO:2200526	http://nanbyodata.jp/ontology/NANDO_2200526	赤色ぼろ線維・ミオクローヌスてんかん症候群	Myoclonus epilepsy associated with ragged-red fibers	H01356	http://www.geneontology.org/formats/oboInOwl#hasDbXref	福原病	MERRF syndrome	https://identifiers.org/kegg.disease:H01356
NANDO:2200526	http://nanbyodata.jp/ontology/NANDO_2200526	赤色ぼろ線維・ミオクローヌスてんかん症候群	Myoclonus epilepsy associated with ragged-red fibers	H01356	http://www.geneontology.org/formats/oboInOwl#hasDbXref	赤色ぼろ線維・ミオクローヌスてんかん症候群	Myoclonic Epilepsy and Ragged-Red Fiber Disease	https://identifiers.org/kegg.disease:H01356
NANDO:2200526	http://nanbyodata.jp/ontology/NANDO_2200526	赤色ぼろ線維・ミオクローヌスてんかん症候群	Myoclonus epilepsy associated with ragged-red fibers	H01356	http://www.geneontology.org/formats/oboInOwl#hasDbXref	MERRF 症候群	Myoclonic Epilepsy and Ragged-Red Fiber Disease	https://identifiers.org/kegg.disease:H01356
NANDO:2200526	http://nanbyodata.jp/ontology/NANDO_2200526	赤色ぼろ線維・ミオクローヌスてんかん症候群	Myoclonus epilepsy associated with ragged-red fibers	H01356	http://www.geneontology.org/formats/oboInOwl#hasDbXref	福原病	Myoclonic Epilepsy and Ragged-Red Fiber Disease	https://identifiers.org/kegg.disease:H01356
NANDO:2200527	http://nanbyodata.jp/ontology/NANDO_2200527	リー症候群	Leigh syndrome	H01354	http://www.geneontology.org/formats/oboInOwl#hasDbXref	リー症候群	Leigh syndrome	https://identifiers.org/kegg.disease:H01354
NANDO:2200529	http://nanbyodata.jp/ontology/NANDO_2200529	カーンズ・セイヤー症候群	Kearns-Sayre syndrome	H01355	http://www.geneontology.org/formats/oboInOwl#hasDbXref	カーンズ・セイアー症候群	Kearns-Sayre syndrome	https://identifiers.org/kegg.disease:H01355
NANDO:2200535	http://nanbyodata.jp/ontology/NANDO_2200535	フルクトース-1,6-ビスホスファターゼ欠損症	Fructose-1,6-bisphosphatase deficiency	H00114	http://www.geneontology.org/formats/oboInOwl#hasDbXref	フルクトース-1,6-ビスホスファターゼ欠損症	Fructose-1,6-bisphosphatase deficiency	https://identifiers.org/kegg.disease:H00114
NANDO:2200545	http://nanbyodata.jp/ontology/NANDO_2200545	グルコーストランスポーター1欠損症	Glucose transporter 1 deficiency	H00836	http://www.geneontology.org/formats/oboInOwl#hasDbXref	グルコーストランスポーター1欠損症	GLUT1 deficiency syndrome	https://identifiers.org/kegg.disease:H00836
NANDO:2200545	http://nanbyodata.jp/ontology/NANDO_2200545	グルコーストランスポーター1欠損症	Glucose transporter 1 deficiency	H00836	http://www.geneontology.org/formats/oboInOwl#hasDbXref	GLUT1欠損症候群	GLUT1 deficiency syndrome	https://identifiers.org/kegg.disease:H00836
NANDO:2200545	http://nanbyodata.jp/ontology/NANDO_2200545	グルコーストランスポーター1欠損症	Glucose transporter 1 deficiency	H00836	http://www.geneontology.org/formats/oboInOwl#hasDbXref	グルコーストランスポーター1欠損症	Glucose transport defect of the blood-brain barrier	https://identifiers.org/kegg.disease:H00836
NANDO:2200545	http://nanbyodata.jp/ontology/NANDO_2200545	グルコーストランスポーター1欠損症	Glucose transporter 1 deficiency	H00836	http://www.geneontology.org/formats/oboInOwl#hasDbXref	GLUT1欠損症候群	Glucose transport defect of the blood-brain barrier	https://identifiers.org/kegg.disease:H00836
NANDO:2200547	http://nanbyodata.jp/ontology/NANDO_2200547	ムコ多糖症I型	Mucopolysaccharidosis type I	H00128	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ハーラー症候群	Mucopolysaccharidosis type I	https://identifiers.org/kegg.disease:H00128
NANDO:2200547	http://nanbyodata.jp/ontology/NANDO_2200547	ムコ多糖症I型	Mucopolysaccharidosis type I	H00128	http://www.geneontology.org/formats/oboInOwl#hasDbXref	シャイエ症候群	Mucopolysaccharidosis type I	https://identifiers.org/kegg.disease:H00128
NANDO:2200547	http://nanbyodata.jp/ontology/NANDO_2200547	ムコ多糖症I型	Mucopolysaccharidosis type I	H00128	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ハーラー・シャイエ症候群	Mucopolysaccharidosis type I	https://identifiers.org/kegg.disease:H00128
NANDO:2200547	http://nanbyodata.jp/ontology/NANDO_2200547	ムコ多糖症I型	Mucopolysaccharidosis type I	H00128	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ムコ多糖症 I 型	Mucopolysaccharidosis type I	https://identifiers.org/kegg.disease:H00128
NANDO:2200547	http://nanbyodata.jp/ontology/NANDO_2200547	ムコ多糖症I型	Mucopolysaccharidosis type I	H00128	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ハーラー症候群	Hurler syndrome	https://identifiers.org/kegg.disease:H00128
NANDO:2200547	http://nanbyodata.jp/ontology/NANDO_2200547	ムコ多糖症I型	Mucopolysaccharidosis type I	H00128	http://www.geneontology.org/formats/oboInOwl#hasDbXref	シャイエ症候群	Hurler syndrome	https://identifiers.org/kegg.disease:H00128
NANDO:2200547	http://nanbyodata.jp/ontology/NANDO_2200547	ムコ多糖症I型	Mucopolysaccharidosis type I	H00128	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ハーラー・シャイエ症候群	Hurler syndrome	https://identifiers.org/kegg.disease:H00128
NANDO:2200547	http://nanbyodata.jp/ontology/NANDO_2200547	ムコ多糖症I型	Mucopolysaccharidosis type I	H00128	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ムコ多糖症 I 型	Hurler syndrome	https://identifiers.org/kegg.disease:H00128
NANDO:2200547	http://nanbyodata.jp/ontology/NANDO_2200547	ムコ多糖症I型	Mucopolysaccharidosis type I	H00128	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ハーラー症候群	Hurler-Scheie syndrome	https://identifiers.org/kegg.disease:H00128
NANDO:2200547	http://nanbyodata.jp/ontology/NANDO_2200547	ムコ多糖症I型	Mucopolysaccharidosis type I	H00128	http://www.geneontology.org/formats/oboInOwl#hasDbXref	シャイエ症候群	Hurler-Scheie syndrome	https://identifiers.org/kegg.disease:H00128
NANDO:2200547	http://nanbyodata.jp/ontology/NANDO_2200547	ムコ多糖症I型	Mucopolysaccharidosis type I	H00128	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ハーラー・シャイエ症候群	Hurler-Scheie syndrome	https://identifiers.org/kegg.disease:H00128
NANDO:2200547	http://nanbyodata.jp/ontology/NANDO_2200547	ムコ多糖症I型	Mucopolysaccharidosis type I	H00128	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ムコ多糖症 I 型	Hurler-Scheie syndrome	https://identifiers.org/kegg.disease:H00128
NANDO:2200547	http://nanbyodata.jp/ontology/NANDO_2200547	ムコ多糖症I型	Mucopolysaccharidosis type I	H00128	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ハーラー症候群	Scheie syndrome	https://identifiers.org/kegg.disease:H00128
NANDO:2200547	http://nanbyodata.jp/ontology/NANDO_2200547	ムコ多糖症I型	Mucopolysaccharidosis type I	H00128	http://www.geneontology.org/formats/oboInOwl#hasDbXref	シャイエ症候群	Scheie syndrome	https://identifiers.org/kegg.disease:H00128
NANDO:2200547	http://nanbyodata.jp/ontology/NANDO_2200547	ムコ多糖症I型	Mucopolysaccharidosis type I	H00128	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ハーラー・シャイエ症候群	Scheie syndrome	https://identifiers.org/kegg.disease:H00128
NANDO:2200547	http://nanbyodata.jp/ontology/NANDO_2200547	ムコ多糖症I型	Mucopolysaccharidosis type I	H00128	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ムコ多糖症 I 型	Scheie syndrome	https://identifiers.org/kegg.disease:H00128
NANDO:2200548	http://nanbyodata.jp/ontology/NANDO_2200548	ムコ多糖症II型	Mucopolysaccharidosis type II	H00129	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ハンター症候群	Hunter syndrome	https://identifiers.org/kegg.disease:H00129
NANDO:2200548	http://nanbyodata.jp/ontology/NANDO_2200548	ムコ多糖症II型	Mucopolysaccharidosis type II	H00129	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ムコ多糖症 II 型	Hunter syndrome	https://identifiers.org/kegg.disease:H00129
NANDO:2200548	http://nanbyodata.jp/ontology/NANDO_2200548	ムコ多糖症II型	Mucopolysaccharidosis type II	H00129	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ハンター症候群	Mucopolysaccharidosis type II	https://identifiers.org/kegg.disease:H00129
NANDO:2200548	http://nanbyodata.jp/ontology/NANDO_2200548	ムコ多糖症II型	Mucopolysaccharidosis type II	H00129	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ムコ多糖症 II 型	Mucopolysaccharidosis type II	https://identifiers.org/kegg.disease:H00129
NANDO:2200549	http://nanbyodata.jp/ontology/NANDO_2200549	ムコ多糖症III型	Mucopolysaccharidosis type III	H00130	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ムコ多糖症 III 型	Mucopolysaccharidosis type III	https://identifiers.org/kegg.disease:H00130
NANDO:2200550	http://nanbyodata.jp/ontology/NANDO_2200550	ムコ多糖症IV型	Mucopolysaccharidosis type IV	H00123	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ムコ多糖症 IV 型	Mucopolysaccharidosis type IV	https://identifiers.org/kegg.disease:H00123
NANDO:2200551	http://nanbyodata.jp/ontology/NANDO_2200551	ムコ多糖症VI型	Mucopolysaccharidosis type VI	H00131	http://www.geneontology.org/formats/oboInOwl#hasDbXref	マロトー・ラミー症候群	Maroteaux-Lamy syndrome	https://identifiers.org/kegg.disease:H00131
NANDO:2200551	http://nanbyodata.jp/ontology/NANDO_2200551	ムコ多糖症VI型	Mucopolysaccharidosis type VI	H00131	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ムコ多糖症 VI 型	Maroteaux-Lamy syndrome	https://identifiers.org/kegg.disease:H00131
NANDO:2200551	http://nanbyodata.jp/ontology/NANDO_2200551	ムコ多糖症VI型	Mucopolysaccharidosis type VI	H00131	http://www.geneontology.org/formats/oboInOwl#hasDbXref	マロトー・ラミー症候群	Mucopolysaccharidosis type VI	https://identifiers.org/kegg.disease:H00131
NANDO:2200551	http://nanbyodata.jp/ontology/NANDO_2200551	ムコ多糖症VI型	Mucopolysaccharidosis type VI	H00131	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ムコ多糖症 VI 型	Mucopolysaccharidosis type VI	https://identifiers.org/kegg.disease:H00131
NANDO:2200552	http://nanbyodata.jp/ontology/NANDO_2200552	ムコ多糖症VII型	Mucopolysaccharidosis type VII	H00132	http://www.geneontology.org/formats/oboInOwl#hasDbXref	スライ症候群	Mucopolysaccharidosis type VII	https://identifiers.org/kegg.disease:H00132
NANDO:2200552	http://nanbyodata.jp/ontology/NANDO_2200552	ムコ多糖症VII型	Mucopolysaccharidosis type VII	H00132	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ムコ多糖症 VII 型	Mucopolysaccharidosis type VII	https://identifiers.org/kegg.disease:H00132
NANDO:2200552	http://nanbyodata.jp/ontology/NANDO_2200552	ムコ多糖症VII型	Mucopolysaccharidosis type VII	H00132	http://www.geneontology.org/formats/oboInOwl#hasDbXref	スライ症候群	Sly syndrome	https://identifiers.org/kegg.disease:H00132
NANDO:2200552	http://nanbyodata.jp/ontology/NANDO_2200552	ムコ多糖症VII型	Mucopolysaccharidosis type VII	H00132	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ムコ多糖症 VII 型	Sly syndrome	https://identifiers.org/kegg.disease:H00132
NANDO:2200555	http://nanbyodata.jp/ontology/NANDO_2200555	アスパルチルグルコサミン尿症	Aspartylglucosaminuria	H00145	http://www.geneontology.org/formats/oboInOwl#hasDbXref	アスパルチルグルコサミン尿症	Aspartylglucosaminuria	https://identifiers.org/kegg.disease:H00145
NANDO:2200556	http://nanbyodata.jp/ontology/NANDO_2200556	シアリドーシス	Sialidosis	H00142	http://www.geneontology.org/formats/oboInOwl#hasDbXref	シアリドーシス	Sialidosis	https://identifiers.org/kegg.disease:H00142
NANDO:2200556	http://nanbyodata.jp/ontology/NANDO_2200556	シアリドーシス	Sialidosis	H00142	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ムコリピドーシス 1 型	Sialidosis	https://identifiers.org/kegg.disease:H00142
NANDO:2200556	http://nanbyodata.jp/ontology/NANDO_2200556	シアリドーシス	Sialidosis	H00142	http://www.geneontology.org/formats/oboInOwl#hasDbXref	シアリドーシス	Mucolipidosis I	https://identifiers.org/kegg.disease:H00142
NANDO:2200556	http://nanbyodata.jp/ontology/NANDO_2200556	シアリドーシス	Sialidosis	H00142	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ムコリピドーシス 1 型	Mucolipidosis I	https://identifiers.org/kegg.disease:H00142
NANDO:2200557	http://nanbyodata.jp/ontology/NANDO_2200557	ガラクトシアリドーシス	Galactosialidosis	H00276	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ガラクトシアリドーシス	Galactosialidosis	https://identifiers.org/kegg.disease:H00276
NANDO:2200557	http://nanbyodata.jp/ontology/NANDO_2200557	ガラクトシアリドーシス	Galactosialidosis	H00276	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ノイラミダーゼ欠損および β-ガラクトシダーゼ欠損症	Galactosialidosis	https://identifiers.org/kegg.disease:H00276
NANDO:2200557	http://nanbyodata.jp/ontology/NANDO_2200557	ガラクトシアリドーシス	Galactosialidosis	H00276	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ガラクトシアリドーシス	Neuraminidase deficiency with beta-galactosidase deficiency	https://identifiers.org/kegg.disease:H00276
NANDO:2200557	http://nanbyodata.jp/ontology/NANDO_2200557	ガラクトシアリドーシス	Galactosialidosis	H00276	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ノイラミダーゼ欠損および β-ガラクトシダーゼ欠損症	Neuraminidase deficiency with beta-galactosidase deficiency	https://identifiers.org/kegg.disease:H00276
NANDO:2200558	http://nanbyodata.jp/ontology/NANDO_2200558	GM1ガングリオシドーシス	GM1 Gangliosidosis	H00281	http://www.geneontology.org/formats/oboInOwl#hasDbXref	GM1 ガングリオシドーシス	GM1 gangliosidosis	https://identifiers.org/kegg.disease:H00281
NANDO:2200560	http://nanbyodata.jp/ontology/NANDO_2200560	異染性白質ジストロフィー	Metachromatic leukodystrophy	H00127	http://www.geneontology.org/formats/oboInOwl#hasDbXref	異染性白質ジストロフィー	Metachromatic leukodystrophy	https://identifiers.org/kegg.disease:H00127
NANDO:2200562	http://nanbyodata.jp/ontology/NANDO_2200562	ゴーシェ病	Gaucher disease	H00126	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ゴーシェ病	Gaucher disease	https://identifiers.org/kegg.disease:H00126
NANDO:2200563	http://nanbyodata.jp/ontology/NANDO_2200563	ファブリー病	Fabry disease	H00125	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ファブリー病	Fabry disease	https://identifiers.org/kegg.disease:H00125
NANDO:2200563	http://nanbyodata.jp/ontology/NANDO_2200563	ファブリー病	Fabry disease	H00125	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ファブリー病	Anderson-Fabry disease	https://identifiers.org/kegg.disease:H00125
NANDO:2200564	http://nanbyodata.jp/ontology/NANDO_2200564	クラッベ病	Krabbe disease	H00135	http://www.geneontology.org/formats/oboInOwl#hasDbXref	クラッベ病	Krabbe disease	https://identifiers.org/kegg.disease:H00135
NANDO:2200564	http://nanbyodata.jp/ontology/NANDO_2200564	クラッベ病	Krabbe disease	H00135	http://www.geneontology.org/formats/oboInOwl#hasDbXref	グロボイド細胞白質ジストロフィー	Krabbe disease	https://identifiers.org/kegg.disease:H00135
NANDO:2200564	http://nanbyodata.jp/ontology/NANDO_2200564	クラッベ病	Krabbe disease	H00135	http://www.geneontology.org/formats/oboInOwl#hasDbXref	クラッベ病	Globoid cell leukodystrophy	https://identifiers.org/kegg.disease:H00135
NANDO:2200564	http://nanbyodata.jp/ontology/NANDO_2200564	クラッベ病	Krabbe disease	H00135	http://www.geneontology.org/formats/oboInOwl#hasDbXref	グロボイド細胞白質ジストロフィー	Globoid cell leukodystrophy	https://identifiers.org/kegg.disease:H00135
NANDO:2200565	http://nanbyodata.jp/ontology/NANDO_2200565	ファーバー病	Farber disease	H00138	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ファーバー病	Farber disease	https://identifiers.org/kegg.disease:H00138
NANDO:2200565	http://nanbyodata.jp/ontology/NANDO_2200565	ファーバー病	Farber disease	H00138	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ファーバー脂肪性肉芽腫症	Farber disease	https://identifiers.org/kegg.disease:H00138
NANDO:2200565	http://nanbyodata.jp/ontology/NANDO_2200565	ファーバー病	Farber disease	H00138	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ファーバー病	Farber lipogranulomatosis	https://identifiers.org/kegg.disease:H00138
NANDO:2200565	http://nanbyodata.jp/ontology/NANDO_2200565	ファーバー病	Farber disease	H00138	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ファーバー脂肪性肉芽腫症	Farber lipogranulomatosis	https://identifiers.org/kegg.disease:H00138
NANDO:2200566	http://nanbyodata.jp/ontology/NANDO_2200566	マルチプルスルファターゼ欠損症	Multiple sulfatase deficiency	H00272	http://www.geneontology.org/formats/oboInOwl#hasDbXref	マルチプルスルファターゼ欠損症	Multiple sulfatase deficiency	https://identifiers.org/kegg.disease:H00272
NANDO:2200567	http://nanbyodata.jp/ontology/NANDO_2200567	ムコリピドーシスII型	Mucolipidosis II	H00143	http://www.geneontology.org/formats/oboInOwl#hasDbXref	I 細胞病	I-cell disease	https://identifiers.org/kegg.disease:H00143
NANDO:2200567	http://nanbyodata.jp/ontology/NANDO_2200567	ムコリピドーシスII型	Mucolipidosis II	H00143	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ムコリピドーシス II 型	I-cell disease	https://identifiers.org/kegg.disease:H00143
NANDO:2200567	http://nanbyodata.jp/ontology/NANDO_2200567	ムコリピドーシスII型	Mucolipidosis II	H00143	http://www.geneontology.org/formats/oboInOwl#hasDbXref	I 細胞病	Mucolipidosis II	https://identifiers.org/kegg.disease:H00143
NANDO:2200567	http://nanbyodata.jp/ontology/NANDO_2200567	ムコリピドーシスII型	Mucolipidosis II	H00143	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ムコリピドーシス II 型	Mucolipidosis II	https://identifiers.org/kegg.disease:H00143
NANDO:2200571	http://nanbyodata.jp/ontology/NANDO_2200571	シスチン症	Cystinosis	H00275	http://www.geneontology.org/formats/oboInOwl#hasDbXref	シスチン症	Cystinosis	https://identifiers.org/kegg.disease:H00275
NANDO:2200573	http://nanbyodata.jp/ontology/NANDO_2200573	神経セロイドリポフスチン症	Neuronal ceroid lipofuscinoses	H00149	http://www.geneontology.org/formats/oboInOwl#hasDbXref	神経セロイドリポフスチン症	Neuronal ceroid lipofuscinosis	https://identifiers.org/kegg.disease:H00149
NANDO:2200575	http://nanbyodata.jp/ontology/NANDO_2200575	ペルオキシソーム形成異常症	Peroxisome biogenesis disorders	H00205	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ペルオキシソーム形成異常症	Peroxisome biogenesis disorder	https://identifiers.org/kegg.disease:H00205
NANDO:2200576	http://nanbyodata.jp/ontology/NANDO_2200576	副腎白質ジストロフィー	Adrenoleukodystrophy	H00176	http://www.geneontology.org/formats/oboInOwl#hasDbXref	副腎白質ジストロフィー	Adrenoleukodystrophy	https://identifiers.org/kegg.disease:H00176
NANDO:2200577	http://nanbyodata.jp/ontology/NANDO_2200577	レフサム病	Refsum disease	H00075	http://www.geneontology.org/formats/oboInOwl#hasDbXref	レフスム病	Refsum disease	https://identifiers.org/kegg.disease:H00075
NANDO:2200577	http://nanbyodata.jp/ontology/NANDO_2200577	レフサム病	Refsum disease	H00075	http://www.geneontology.org/formats/oboInOwl#hasDbXref	多発神経炎型遺伝性失調症	Refsum disease	https://identifiers.org/kegg.disease:H00075
NANDO:2200577	http://nanbyodata.jp/ontology/NANDO_2200577	レフサム病	Refsum disease	H00075	http://www.geneontology.org/formats/oboInOwl#hasDbXref	レフスム病	Heredopathia atactica polyneuritiformis	https://identifiers.org/kegg.disease:H00075
NANDO:2200577	http://nanbyodata.jp/ontology/NANDO_2200577	レフサム病	Refsum disease	H00075	http://www.geneontology.org/formats/oboInOwl#hasDbXref	多発神経炎型遺伝性失調症	Heredopathia atactica polyneuritiformis	https://identifiers.org/kegg.disease:H00075
NANDO:2200579	http://nanbyodata.jp/ontology/NANDO_2200579	ウィルソン病	Wilson disease	H00210	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ウィルソン病	Wilson disease	https://identifiers.org/kegg.disease:H00210
NANDO:2200579	http://nanbyodata.jp/ontology/NANDO_2200579	ウィルソン病	Wilson disease	H00210	http://www.geneontology.org/formats/oboInOwl#hasDbXref	肝レンズ核変性症	Wilson disease	https://identifiers.org/kegg.disease:H00210
NANDO:2200579	http://nanbyodata.jp/ontology/NANDO_2200579	ウィルソン病	Wilson disease	H00210	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ウィルソン病	Hepatolenticular degeneration	https://identifiers.org/kegg.disease:H00210
NANDO:2200579	http://nanbyodata.jp/ontology/NANDO_2200579	ウィルソン病	Wilson disease	H00210	http://www.geneontology.org/formats/oboInOwl#hasDbXref	肝レンズ核変性症	Hepatolenticular degeneration	https://identifiers.org/kegg.disease:H00210
NANDO:2200583	http://nanbyodata.jp/ontology/NANDO_2200583	亜硫酸酸化酵素欠損症	Sulfite oxidase deficiency	H01237	http://www.geneontology.org/formats/oboInOwl#hasDbXref	亜硫酸オキシダーゼ欠損症	Sulfite oxidase deficiency	https://identifiers.org/kegg.disease:H01237
NANDO:2200586	http://nanbyodata.jp/ontology/NANDO_2200586	ヒポキサンチングアニンホスホリボシルトランスフェラーゼ欠損症	Lesch-Nyhan syndrome	H00194	http://www.geneontology.org/formats/oboInOwl#hasDbXref	レッシュ・ナイハン症候群	Lesch-Nyhan syndrome	https://identifiers.org/kegg.disease:H00194
NANDO:2200586	http://nanbyodata.jp/ontology/NANDO_2200586	ヒポキサンチングアニンホスホリボシルトランスフェラーゼ欠損症	Lesch-Nyhan syndrome	H00194	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ヒポキサンチン・グアニンホスホリボシルトランスフェラーゼ欠損症	Lesch-Nyhan syndrome	https://identifiers.org/kegg.disease:H00194
NANDO:2200586	http://nanbyodata.jp/ontology/NANDO_2200586	ヒポキサンチングアニンホスホリボシルトランスフェラーゼ欠損症	Lesch-Nyhan syndrome	H00194	http://www.geneontology.org/formats/oboInOwl#hasDbXref	レッシュ・ナイハン症候群	Hypoxanthine-guanine phosophoribosyltransferase deficiency	https://identifiers.org/kegg.disease:H00194
NANDO:2200586	http://nanbyodata.jp/ontology/NANDO_2200586	ヒポキサンチングアニンホスホリボシルトランスフェラーゼ欠損症	Lesch-Nyhan syndrome	H00194	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ヒポキサンチン・グアニンホスホリボシルトランスフェラーゼ欠損症	Hypoxanthine-guanine phosophoribosyltransferase deficiency	https://identifiers.org/kegg.disease:H00194
NANDO:2200587	http://nanbyodata.jp/ontology/NANDO_2200587	アデニンホスホリボシルトランスフェラーゼ欠損症	Adenine phosphoribosyltransferase deficiency	H00195	http://www.geneontology.org/formats/oboInOwl#hasDbXref	アデニンホスホリボシルトランスフェラーゼ欠損症	Adenine phosphoribosyltransferase deficiency	https://identifiers.org/kegg.disease:H00195
NANDO:2200587	http://nanbyodata.jp/ontology/NANDO_2200587	アデニンホスホリボシルトランスフェラーゼ欠損症	Adenine phosphoribosyltransferase deficiency	H00195	http://www.geneontology.org/formats/oboInOwl#hasDbXref	2-8ジヒドロキシアデニン結石	Adenine phosphoribosyltransferase deficiency	https://identifiers.org/kegg.disease:H00195
NANDO:2200587	http://nanbyodata.jp/ontology/NANDO_2200587	アデニンホスホリボシルトランスフェラーゼ欠損症	Adenine phosphoribosyltransferase deficiency	H00195	http://www.geneontology.org/formats/oboInOwl#hasDbXref	アデニンホスホリボシルトランスフェラーゼ欠損症	2,8-Dihydroxyadenine urolithiasis	https://identifiers.org/kegg.disease:H00195
NANDO:2200587	http://nanbyodata.jp/ontology/NANDO_2200587	アデニンホスホリボシルトランスフェラーゼ欠損症	Adenine phosphoribosyltransferase deficiency	H00195	http://www.geneontology.org/formats/oboInOwl#hasDbXref	2-8ジヒドロキシアデニン結石	2,8-Dihydroxyadenine urolithiasis	https://identifiers.org/kegg.disease:H00195
NANDO:2200588	http://nanbyodata.jp/ontology/NANDO_2200588	キサンチン尿症	Xanthinuria	H00192	http://www.geneontology.org/formats/oboInOwl#hasDbXref	キサンチン尿症	Xanthinuria	https://identifiers.org/kegg.disease:H00192
NANDO:2200590	http://nanbyodata.jp/ontology/NANDO_2200590	オロト酸尿症	Orotic aciduria	H00198	http://www.geneontology.org/formats/oboInOwl#hasDbXref	オロト酸尿症	Orotic aciduria	https://identifiers.org/kegg.disease:H00198
NANDO:2200592	http://nanbyodata.jp/ontology/NANDO_2200592	先天性葉酸吸収不全症	Hereditary folate malabsorption	H01252	http://www.geneontology.org/formats/oboInOwl#hasDbXref	先天性葉酸吸収不全	Hereditary folate malabsorption	https://identifiers.org/kegg.disease:H01252
NANDO:2200596	http://nanbyodata.jp/ontology/NANDO_2200596	芳香族L－アミノ酸脱炭酸酵素欠損症	Aromatic L-amino acid decarboxylase deficiency	H01161	http://www.geneontology.org/formats/oboInOwl#hasDbXref	AADC欠損症	Aromatic L-amino acid decarboxylase deficiency	https://identifiers.org/kegg.disease:H01161
NANDO:2200596	http://nanbyodata.jp/ontology/NANDO_2200596	芳香族L－アミノ酸脱炭酸酵素欠損症	Aromatic L-amino acid decarboxylase deficiency	H01161	http://www.geneontology.org/formats/oboInOwl#hasDbXref	芳香族 L- アミノ酸脱炭酸酵素欠損症	Aromatic L-amino acid decarboxylase deficiency	https://identifiers.org/kegg.disease:H01161
NANDO:2200599	http://nanbyodata.jp/ontology/NANDO_2200599	コハク酸セミアルデヒド脱水素酵素欠損症	Succinic semialdehyde dehydrogenase deficiency	H00835	http://www.geneontology.org/formats/oboInOwl#hasDbXref	コハク酸セミアルデヒド脱水素酵素欠損症	Succinic semialdehyde dehydrogenase deficiency	https://identifiers.org/kegg.disease:H00835
NANDO:2200599	http://nanbyodata.jp/ontology/NANDO_2200599	コハク酸セミアルデヒド脱水素酵素欠損症	Succinic semialdehyde dehydrogenase deficiency	H00835	http://www.geneontology.org/formats/oboInOwl#hasDbXref	4-ヒドロキシ酪酸尿症	Succinic semialdehyde dehydrogenase deficiency	https://identifiers.org/kegg.disease:H00835
NANDO:2200599	http://nanbyodata.jp/ontology/NANDO_2200599	コハク酸セミアルデヒド脱水素酵素欠損症	Succinic semialdehyde dehydrogenase deficiency	H00835	http://www.geneontology.org/formats/oboInOwl#hasDbXref	コハク酸セミアルデヒド脱水素酵素欠損症	4-Hydroxybutyric aciduria	https://identifiers.org/kegg.disease:H00835
NANDO:2200599	http://nanbyodata.jp/ontology/NANDO_2200599	コハク酸セミアルデヒド脱水素酵素欠損症	Succinic semialdehyde dehydrogenase deficiency	H00835	http://www.geneontology.org/formats/oboInOwl#hasDbXref	4-ヒドロキシ酪酸尿症	4-Hydroxybutyric aciduria	https://identifiers.org/kegg.disease:H00835
NANDO:2200601	http://nanbyodata.jp/ontology/NANDO_2200601	原発性高カイロミクロン血症	Primary hyperchylomicronemia	H01784	http://www.geneontology.org/formats/oboInOwl#hasDbXref	原発性高カイロミクロン血症	Primary hyperchylomicronemia	https://identifiers.org/kegg.disease:H01784
NANDO:2200602	http://nanbyodata.jp/ontology/NANDO_2200602	家族性高コレステロール血症	Familial hypercholesterolemia	H00155	http://www.geneontology.org/formats/oboInOwl#hasDbXref	家族性高コレステロール血症	Familial hypercholesterolemia	https://identifiers.org/kegg.disease:H00155
NANDO:2200602	http://nanbyodata.jp/ontology/NANDO_2200602	家族性高コレステロール血症	Familial hypercholesterolemia	H00155	http://www.geneontology.org/formats/oboInOwl#hasDbXref	家族性高コレステロール血症	Autosomal dominant hypercholesterolaemia	https://identifiers.org/kegg.disease:H00155
NANDO:2200603	http://nanbyodata.jp/ontology/NANDO_2200603	家族性複合型高脂血症	Familial combined hyperlipidemia	H00153	http://www.geneontology.org/formats/oboInOwl#hasDbXref	家族性複合型高脂血症	Familial combined hyperlipidemia	https://identifiers.org/kegg.disease:H00153
NANDO:2200604	http://nanbyodata.jp/ontology/NANDO_2200604	無βリポタンパク血症	Abetalipoproteinemia	H00160	http://www.geneontology.org/formats/oboInOwl#hasDbXref	無βリポタンパク血症	Abetalipoproteinemia	https://identifiers.org/kegg.disease:H00160
NANDO:2200604	http://nanbyodata.jp/ontology/NANDO_2200604	無βリポタンパク血症	Abetalipoproteinemia	H00160	http://www.geneontology.org/formats/oboInOwl#hasDbXref	バッセン・コーンツヴァイク病	Abetalipoproteinemia	https://identifiers.org/kegg.disease:H00160
NANDO:2200604	http://nanbyodata.jp/ontology/NANDO_2200604	無βリポタンパク血症	Abetalipoproteinemia	H00160	http://www.geneontology.org/formats/oboInOwl#hasDbXref	無βリポタンパク血症	Bassen-Kornzweig Disease	https://identifiers.org/kegg.disease:H00160
NANDO:2200604	http://nanbyodata.jp/ontology/NANDO_2200604	無βリポタンパク血症	Abetalipoproteinemia	H00160	http://www.geneontology.org/formats/oboInOwl#hasDbXref	バッセン・コーンツヴァイク病	Bassen-Kornzweig Disease	https://identifiers.org/kegg.disease:H00160
NANDO:2200607	http://nanbyodata.jp/ontology/NANDO_2200607	エーラス・ダンロス症候群	Ehlers-Danlos syndrome	H00802	http://www.geneontology.org/formats/oboInOwl#hasDbXref	エーラス・ダンロス症候群	Ehlers-Danlos syndrome	https://identifiers.org/kegg.disease:H00802
NANDO:2200611	http://nanbyodata.jp/ontology/NANDO_2200611	α1-アンチトリプシン欠損症	Alpha-1-antitrypsin deficiency	H01103	http://www.geneontology.org/formats/oboInOwl#hasDbXref	α1-アンチトリプシン欠乏症	Alpha-1-antitrypsin deficiency	https://identifiers.org/kegg.disease:H01103
NANDO:2200613	http://nanbyodata.jp/ontology/NANDO_2200613	後天性赤芽球癆	Acquired pure red cell aplasia	H01586	http://www.geneontology.org/formats/oboInOwl#hasDbXref	後天性赤芽球癆	Acquired pure red cell aplasia	https://identifiers.org/kegg.disease:H01586
NANDO:2200615	http://nanbyodata.jp/ontology/NANDO_2200615	先天性赤血球形成異常性貧血	Congenital dyserythropoietic anemia	H00917	http://www.geneontology.org/formats/oboInOwl#hasDbXref	先天性赤血球形成異常性貧血	Congenital dyserythropoietic anemia	https://identifiers.org/kegg.disease:H00917
NANDO:2200615	http://nanbyodata.jp/ontology/NANDO_2200615	先天性赤血球形成異常性貧血	Congenital dyserythropoietic anemia	H00917	http://www.geneontology.org/formats/oboInOwl#hasDbXref	先天性赤血球生成不全性貧血	Congenital dyserythropoietic anemia	https://identifiers.org/kegg.disease:H00917
NANDO:2200615	http://nanbyodata.jp/ontology/NANDO_2200615	先天性赤血球形成異常性貧血	Congenital dyserythropoietic anemia	H00917	http://www.geneontology.org/formats/oboInOwl#hasDbXref	先天性赤血球異形成貧血	Congenital dyserythropoietic anemia	https://identifiers.org/kegg.disease:H00917
NANDO:2200617	http://nanbyodata.jp/ontology/NANDO_2200617	無トランスフェリン血症	Congenital atransferrinemia	H01145	http://www.geneontology.org/formats/oboInOwl#hasDbXref	無トランスフェリン血症	Congenital hypotransferrinemia	https://identifiers.org/kegg.disease:H01145
NANDO:2200617	http://nanbyodata.jp/ontology/NANDO_2200617	無トランスフェリン血症	Congenital atransferrinemia	H01145	http://www.geneontology.org/formats/oboInOwl#hasDbXref	無トランスフェリン血症	Atransferrinemia	https://identifiers.org/kegg.disease:H01145
NANDO:2200621	http://nanbyodata.jp/ontology/NANDO_2200621	発作性夜間ヘモグロビン尿症	Paroxysmal nocturnal hemoglobinuria	H01053	http://www.geneontology.org/formats/oboInOwl#hasDbXref	発作性夜間ヘモグロビン尿症	Paroxysmal nocturnal hemoglobinuria	https://identifiers.org/kegg.disease:H01053
NANDO:2200622	http://nanbyodata.jp/ontology/NANDO_2200622	遺伝性球状赤血球症	Hereditary spherocytosis	H00230	http://www.geneontology.org/formats/oboInOwl#hasDbXref	遺伝性球状赤血球症	Hereditary spherocytosis	https://identifiers.org/kegg.disease:H00230
NANDO:2200626	http://nanbyodata.jp/ontology/NANDO_2200626	サラセミア	Thalassemia	H00228	http://www.geneontology.org/formats/oboInOwl#hasDbXref	サラセミア	Thalassemia	https://identifiers.org/kegg.disease:H00228
NANDO:2200630	http://nanbyodata.jp/ontology/NANDO_2200630	遺伝性楕円赤血球症	Hereditary elliptocytosis	H00231	http://www.geneontology.org/formats/oboInOwl#hasDbXref	遺伝性楕円赤血球症	Hereditary elliptocytosis	https://identifiers.org/kegg.disease:H00231
NANDO:2200639	http://nanbyodata.jp/ontology/NANDO_2200639	播種性血管内凝固症候群	Disseminated intravascular coagulation	H01587	http://www.geneontology.org/formats/oboInOwl#hasDbXref	播種性血管内凝固症候群	Disseminated intravascular coagulation	https://identifiers.org/kegg.disease:H01587
NANDO:2200639	http://nanbyodata.jp/ontology/NANDO_2200639	播種性血管内凝固症候群	Disseminated intravascular coagulation	H01587	http://www.geneontology.org/formats/oboInOwl#hasDbXref	汎発性血管内凝固症候群	Disseminated intravascular coagulation	https://identifiers.org/kegg.disease:H01587
NANDO:2200644	http://nanbyodata.jp/ontology/NANDO_2200644	家族性赤血球増加症	Familial polycythemia	H00236	http://www.geneontology.org/formats/oboInOwl#hasDbXref	家族性赤血球増加症	Congenital polycythemia	https://identifiers.org/kegg.disease:H00236
NANDO:2200644	http://nanbyodata.jp/ontology/NANDO_2200644	家族性赤血球増加症	Familial polycythemia	H00236	http://www.geneontology.org/formats/oboInOwl#hasDbXref	先天性赤血球増加症	Congenital polycythemia	https://identifiers.org/kegg.disease:H00236
NANDO:2200644	http://nanbyodata.jp/ontology/NANDO_2200644	家族性赤血球増加症	Familial polycythemia	H00236	http://www.geneontology.org/formats/oboInOwl#hasDbXref	家族性赤血球増加症	Familial erythrocytosis (ECYT)	https://identifiers.org/kegg.disease:H00236
NANDO:2200644	http://nanbyodata.jp/ontology/NANDO_2200644	家族性赤血球増加症	Familial polycythemia	H00236	http://www.geneontology.org/formats/oboInOwl#hasDbXref	先天性赤血球増加症	Familial erythrocytosis (ECYT)	https://identifiers.org/kegg.disease:H00236
NANDO:2200649	http://nanbyodata.jp/ontology/NANDO_2200649	血栓性血小板減少性紫斑病	Thrombotic thrombocytopenic purpura	H00225	http://www.geneontology.org/formats/oboInOwl#hasDbXref	血栓性血小板減少性紫斑病	Thrombotic thrombocytopenic purpura	https://identifiers.org/kegg.disease:H00225
NANDO:2200649	http://nanbyodata.jp/ontology/NANDO_2200649	血栓性血小板減少性紫斑病	Thrombotic thrombocytopenic purpura	H00225	http://www.geneontology.org/formats/oboInOwl#hasDbXref	血栓性血小板減少性紫斑病	Moschcowitz disease	https://identifiers.org/kegg.disease:H00225
NANDO:2200649	http://nanbyodata.jp/ontology/NANDO_2200649	血栓性血小板減少性紫斑病	Thrombotic thrombocytopenic purpura	H00225	http://www.geneontology.org/formats/oboInOwl#hasDbXref	血栓性血小板減少性紫斑病	Schulman-Upshaw syndrome	https://identifiers.org/kegg.disease:H00225
NANDO:2200651	http://nanbyodata.jp/ontology/NANDO_2200651	先天性無巨核球性血小板減少症	Congenital amegakaryocytic thrombocytopenia	H00227	http://www.geneontology.org/formats/oboInOwl#hasDbXref	先天性無巨核球性血小板減少症	Congenital amegakaryocytic thrombocytopenia	https://identifiers.org/kegg.disease:H00227
NANDO:2200652	http://nanbyodata.jp/ontology/NANDO_2200652	ファンコニ貧血	Fanconi anemia	H00238	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ファンコニ貧血	Fanconi anemia	https://identifiers.org/kegg.disease:H00238
NANDO:2200655	http://nanbyodata.jp/ontology/NANDO_2200655	本態性血小板血症	Essential thrombocythemia	H01612	http://www.geneontology.org/formats/oboInOwl#hasDbXref	本態性血小板血症	Essential thrombocythemia	https://identifiers.org/kegg.disease:H01612
NANDO:2200655	http://nanbyodata.jp/ontology/NANDO_2200655	本態性血小板血症	Essential thrombocythemia	H01612	http://www.geneontology.org/formats/oboInOwl#hasDbXref	本態性血小板血症	Essential thrombocytosis	https://identifiers.org/kegg.disease:H01612
NANDO:2200655	http://nanbyodata.jp/ontology/NANDO_2200655	本態性血小板血症	Essential thrombocythemia	H01612	http://www.geneontology.org/formats/oboInOwl#hasDbXref	本態性血小板血症	Thrombocythemia	https://identifiers.org/kegg.disease:H01612
NANDO:2200656	http://nanbyodata.jp/ontology/NANDO_2200656	ベルナール・スーリエ症候群	Bernard-Soulier syndrome	H00224	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ベルナール・スーリエ症候群	Bernard-Soulier syndrome	https://identifiers.org/kegg.disease:H00224
NANDO:2200656	http://nanbyodata.jp/ontology/NANDO_2200656	ベルナール・スーリエ症候群	Bernard-Soulier syndrome	H00224	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ベルナール・スーリエ症候群	Giant platelet syndrome	https://identifiers.org/kegg.disease:H00224
NANDO:2200671	http://nanbyodata.jp/ontology/NANDO_2200671	スコット症候群	Scott syndrome	H01162	http://www.geneontology.org/formats/oboInOwl#hasDbXref	スコット症候群	Scott syndrome	https://identifiers.org/kegg.disease:H01162
NANDO:2200674	http://nanbyodata.jp/ontology/NANDO_2200674	第V因子欠乏症	Factor V deficiency	H00220	http://www.geneontology.org/formats/oboInOwl#hasDbXref	第V因子欠損症	Factor V deficiency	https://identifiers.org/kegg.disease:H00220
NANDO:2200674	http://nanbyodata.jp/ontology/NANDO_2200674	第V因子欠乏症	Factor V deficiency	H00220	http://www.geneontology.org/formats/oboInOwl#hasDbXref	第V因子欠損症	Owren disease	https://identifiers.org/kegg.disease:H00220
NANDO:2200692	http://nanbyodata.jp/ontology/NANDO_2200692	骨髄線維症	Myelofibrosis	H01605	http://www.geneontology.org/formats/oboInOwl#hasDbXref	骨髄線維症	Myelofibrosis	https://identifiers.org/kegg.disease:H01605
NANDO:2200693	http://nanbyodata.jp/ontology/NANDO_2200693	再生不良性貧血	Aplastic anemia	H01132	http://www.geneontology.org/formats/oboInOwl#hasDbXref	再生不良性貧血	Aplastic anemia	https://identifiers.org/kegg.disease:H01132
NANDO:2200695	http://nanbyodata.jp/ontology/NANDO_2200695	細網異形成症	Reticular dysgenesis	H01128	http://www.geneontology.org/formats/oboInOwl#hasDbXref	細網異形成症	Reticular dysgenesis	https://identifiers.org/kegg.disease:H01128
NANDO:2200704	http://nanbyodata.jp/ontology/NANDO_2200704	ウィスコット・オルドリッチ症候群	Wiskott-Aldrich syndrome	H01523	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ウィスコット・アルドリッチ症候群	Wiskott-Aldrich syndrome	https://identifiers.org/kegg.disease:H01523
NANDO:2200705	http://nanbyodata.jp/ontology/NANDO_2200705	毛細血管拡張性運動失調症	Ataxia telangiectasia	H00064	http://www.geneontology.org/formats/oboInOwl#hasDbXref	毛細血管拡張性運動失調症	Ataxia telangiectasia	https://identifiers.org/kegg.disease:H00064
NANDO:2200705	http://nanbyodata.jp/ontology/NANDO_2200705	毛細血管拡張性運動失調症	Ataxia telangiectasia	H00064	http://www.geneontology.org/formats/oboInOwl#hasDbXref	毛細血管拡張性運動失調症	Louis-Bar syndrome	https://identifiers.org/kegg.disease:H00064
NANDO:2200705	http://nanbyodata.jp/ontology/NANDO_2200705	毛細血管拡張性運動失調症	Ataxia telangiectasia	H00064	http://www.geneontology.org/formats/oboInOwl#hasDbXref	毛細血管拡張性運動失調症	Boder-Sedgwick syndrome	https://identifiers.org/kegg.disease:H00064
NANDO:2200706	http://nanbyodata.jp/ontology/NANDO_2200706	ナイミーヘン染色体不安定症候群	Nijmegen breakage syndrome	H01344	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ナイミーヘン染色体不安定症候群	Nijmegen breakage syndrome	https://identifiers.org/kegg.disease:H01344
NANDO:2200707	http://nanbyodata.jp/ontology/NANDO_2200707	ブルーム症候群	Bloom syndrome	H01346	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ブルーム症候群	Bloom syndrome	https://identifiers.org/kegg.disease:H01346
NANDO:2200707	http://nanbyodata.jp/ontology/NANDO_2200707	ブルーム症候群	Bloom syndrome	H01346	http://www.geneontology.org/formats/oboInOwl#hasDbXref	MGRISCE1	Bloom syndrome	https://identifiers.org/kegg.disease:H01346
NANDO:2200707	http://nanbyodata.jp/ontology/NANDO_2200707	ブルーム症候群	Bloom syndrome	H01346	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ブルーム症候群	MGRISCE1	https://identifiers.org/kegg.disease:H01346
NANDO:2200707	http://nanbyodata.jp/ontology/NANDO_2200707	ブルーム症候群	Bloom syndrome	H01346	http://www.geneontology.org/formats/oboInOwl#hasDbXref	MGRISCE1	MGRISCE1	https://identifiers.org/kegg.disease:H01346
NANDO:2200710	http://nanbyodata.jp/ontology/NANDO_2200710	RIDDLE症候群	RIDDLE syndrome	H00962	http://www.geneontology.org/formats/oboInOwl#hasDbXref	RIDDLE 症候群	RIDDLE syndrome	https://identifiers.org/kegg.disease:H00962
NANDO:2200715	http://nanbyodata.jp/ontology/NANDO_2200715	先天性角化異常症	Dyskeratosis congenita	H00507	http://www.geneontology.org/formats/oboInOwl#hasDbXref	先天性角化異常症	Dyskeratosis congenita	https://identifiers.org/kegg.disease:H00507
NANDO:2200717	http://nanbyodata.jp/ontology/NANDO_2200717	分類不能型免疫不全症	Common variable immunodeficiency	H00088	http://www.geneontology.org/formats/oboInOwl#hasDbXref	分類不能型免疫不全症	Common variable immunodeficiency	https://identifiers.org/kegg.disease:H00088
NANDO:2200726	http://nanbyodata.jp/ontology/NANDO_2200726	自己免疫性リンパ増殖症候群	Autoimmune lymphoproliferative syndrome	H00108	http://www.geneontology.org/formats/oboInOwl#hasDbXref	自己免疫性リンパ増殖症候群	Autoimmune lymphoproliferative syndromes	https://identifiers.org/kegg.disease:H00108
NANDO:2200751	http://nanbyodata.jp/ontology/NANDO_2200751	Barth症候群	Barth syndrome	H00654	http://www.geneontology.org/formats/oboInOwl#hasDbXref	バース症候群	Barth syndrome	https://identifiers.org/kegg.disease:H00654
NANDO:2200752	http://nanbyodata.jp/ontology/NANDO_2200752	P14欠損症	P14 deficiency	H01218	http://www.geneontology.org/formats/oboInOwl#hasDbXref	P14 欠損症	P14 deficiency	https://identifiers.org/kegg.disease:H01218
NANDO:2200756	http://nanbyodata.jp/ontology/NANDO_2200756	シュワッハマン・ダイアモンド症候群	Shwachman-Diamond syndrome	H00439	http://www.geneontology.org/formats/oboInOwl#hasDbXref	シュバッハマン・ダイアモンド症候群	Shwachman-Diamond syndrome	https://identifiers.org/kegg.disease:H00439
NANDO:2200757	http://nanbyodata.jp/ontology/NANDO_2200757	慢性肉芽腫症	Chronic granulomatous disease	H00098	http://www.geneontology.org/formats/oboInOwl#hasDbXref	慢性肉芽腫症	Chronic granulomatous disease	https://identifiers.org/kegg.disease:H00098
NANDO:2200764	http://nanbyodata.jp/ontology/NANDO_2200764	慢性皮膚粘膜カンジダ症	Chronic mucocutaneous candidiasis	H01109	http://www.geneontology.org/formats/oboInOwl#hasDbXref	慢性皮膚粘膜カンジダ症	Chronic mucocutaneous candidiasis	https://identifiers.org/kegg.disease:H01109
NANDO:2200764	http://nanbyodata.jp/ontology/NANDO_2200764	慢性皮膚粘膜カンジダ症	Chronic mucocutaneous candidiasis	H01109	http://www.geneontology.org/formats/oboInOwl#hasDbXref	慢性皮膚粘膜カンジダ症	Familial candidiasis (CANDF)	https://identifiers.org/kegg.disease:H01109
NANDO:2200767	http://nanbyodata.jp/ontology/NANDO_2200767	WHIM症候群	WHIM syndrome	H00097	http://www.geneontology.org/formats/oboInOwl#hasDbXref	WHIM 症候群	WHIM syndrome	https://identifiers.org/kegg.disease:H00097
NANDO:2200768	http://nanbyodata.jp/ontology/NANDO_2200768	疣贅状表皮発育異常症	Epidermodysplasia verruciformis	H00842	http://www.geneontology.org/formats/oboInOwl#hasDbXref	疣贅状表皮発育異常症	Epidermodysplasia verruciformis	https://identifiers.org/kegg.disease:H00842
NANDO:2200795	http://nanbyodata.jp/ontology/NANDO_2200795	遺伝性血管性浮腫	Hereditary angioedema	H01006	http://www.geneontology.org/formats/oboInOwl#hasDbXref	遺伝性血管性浮腫	Hereditary angioedema	https://identifiers.org/kegg.disease:H01006
NANDO:2200807	http://nanbyodata.jp/ontology/NANDO_2200807	好酸球性消化管疾患	Eosinophilic gastrointestinal disorders	H01782	http://www.geneontology.org/formats/oboInOwl#hasDbXref	好酸球性消化管疾患	Eosinophilic gastrointestinal disorder	https://identifiers.org/kegg.disease:H01782
NANDO:2200817	http://nanbyodata.jp/ontology/NANDO_2200817	滑脳症	Lissencephaly	H00268	http://www.geneontology.org/formats/oboInOwl#hasDbXref	滑脳症	Lissencephaly	https://identifiers.org/kegg.disease:H00268
NANDO:2200818	http://nanbyodata.jp/ontology/NANDO_2200818	裂脳症	Schizencephaly	H01160	http://www.geneontology.org/formats/oboInOwl#hasDbXref	裂脳症	Schizencephaly	https://identifiers.org/kegg.disease:H01160
NANDO:2200819	http://nanbyodata.jp/ontology/NANDO_2200819	全前脳胞症	Holoprosencephaly	H00267	http://www.geneontology.org/formats/oboInOwl#hasDbXref	全前脳胞症	Holoprosencephaly	https://identifiers.org/kegg.disease:H00267
NANDO:2200820	http://nanbyodata.jp/ontology/NANDO_2200820	中隔視神経形成異常症	Septo-optic dysplasia	H00544	http://www.geneontology.org/formats/oboInOwl#hasDbXref	中隔視神経形成異常症	Septo-optic dysplasia	https://identifiers.org/kegg.disease:H00544
NANDO:2200821	http://nanbyodata.jp/ontology/NANDO_2200821	ダンディー・ウォーカー症候群	Dandy-Walker syndrome	H01678	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ダンディ・ウォーカー症候群	Dandy-Walker syndrome	https://identifiers.org/kegg.disease:H01678
NANDO:2200822	http://nanbyodata.jp/ontology/NANDO_2200822	先天性水頭症	Congenital hydrocephalus	H01677	http://www.geneontology.org/formats/oboInOwl#hasDbXref	先天性水頭症	Congenital hydrocephalus	https://identifiers.org/kegg.disease:H01677
NANDO:2200824	http://nanbyodata.jp/ontology/NANDO_2200824	ジュベール症候群関連疾患	Joubert syndrome related disorders	H00530	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ジュベール症候群関連疾患	Joubert syndrome and related disorders	https://identifiers.org/kegg.disease:H00530
NANDO:2200825	http://nanbyodata.jp/ontology/NANDO_2200825	レット症候群	Rett syndrome	H00440	http://www.geneontology.org/formats/oboInOwl#hasDbXref	レット症候群	Rett syndrome	https://identifiers.org/kegg.disease:H00440
NANDO:2200826	http://nanbyodata.jp/ontology/NANDO_2200826	結節性硬化症	Tuberous sclerosis complex	H00915	http://www.geneontology.org/formats/oboInOwl#hasDbXref	結節性硬化症	Tuberous sclerosis complex	https://identifiers.org/kegg.disease:H00915
NANDO:2200826	http://nanbyodata.jp/ontology/NANDO_2200826	結節性硬化症	Tuberous sclerosis complex	H00915	http://www.geneontology.org/formats/oboInOwl#hasDbXref	結節性硬化症	Bourneville-Pringle disease	https://identifiers.org/kegg.disease:H00915
NANDO:2200828	http://nanbyodata.jp/ontology/NANDO_2200828	ゴーリン症候群	Gorlin syndrome	H00895	http://www.geneontology.org/formats/oboInOwl#hasDbXref	基底細胞母斑症候群	Basal cell nevus syndrome	https://identifiers.org/kegg.disease:H00895
NANDO:2200828	http://nanbyodata.jp/ontology/NANDO_2200828	ゴーリン症候群	Gorlin syndrome	H00895	http://www.geneontology.org/formats/oboInOwl#hasDbXref	基底細胞母斑症候群	Gorlin syndrome	https://identifiers.org/kegg.disease:H00895
NANDO:2200828	http://nanbyodata.jp/ontology/NANDO_2200828	ゴーリン症候群	Gorlin syndrome	H00895	http://www.geneontology.org/formats/oboInOwl#hasDbXref	基底細胞母斑症候群	Nevoid basal cell carcinoma syndrome	https://identifiers.org/kegg.disease:H00895
NANDO:2200830	http://nanbyodata.jp/ontology/NANDO_2200830	スタージ・ウェーバー症候群	Sturge-Weber syndrome	H01809	http://www.geneontology.org/formats/oboInOwl#hasDbXref	スタージ・ウェーバー症候群	Sturge-Weber syndrome	https://identifiers.org/kegg.disease:H01809
NANDO:2200831	http://nanbyodata.jp/ontology/NANDO_2200831	ウェルナー症候群	Werner syndrome	H01733	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ウェルナー症候群	Werner syndrome	https://identifiers.org/kegg.disease:H01733
NANDO:2200832	http://nanbyodata.jp/ontology/NANDO_2200832	コケイン症候群	Cockayne syndrome	H00076	http://www.geneontology.org/formats/oboInOwl#hasDbXref	コケイン症候群	Cockayne syndrome	https://identifiers.org/kegg.disease:H00076
NANDO:2200833	http://nanbyodata.jp/ontology/NANDO_2200833	ハッチンソン・ギルフォード症候群	Hutchinson-Gilford syndrome	H00601	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ハッチンソン・ギルフォード症候群	Hutchinson-Gilford progeria syndrome	https://identifiers.org/kegg.disease:H00601
NANDO:2200834	http://nanbyodata.jp/ontology/NANDO_2200834	カナバン病	Canavan disease	H00074	http://www.geneontology.org/formats/oboInOwl#hasDbXref	カナバン病	Canavan disease	https://identifiers.org/kegg.disease:H00074
NANDO:2200835	http://nanbyodata.jp/ontology/NANDO_2200835	アレキサンダー病	Alexander disease	H00065	http://www.geneontology.org/formats/oboInOwl#hasDbXref	アレキサンダー病	Alexander disease	https://identifiers.org/kegg.disease:H00065
NANDO:2200836	http://nanbyodata.jp/ontology/NANDO_2200836	先天性大脳白質形成不全症	Congenital hypomyelinating leukodystrophy	H00679	http://www.geneontology.org/formats/oboInOwl#hasDbXref	先天性大脳白質形成不全症	Hypomyelinating leukodystrophy	https://identifiers.org/kegg.disease:H00679
NANDO:2200836	http://nanbyodata.jp/ontology/NANDO_2200836	先天性大脳白質形成不全症	Congenital hypomyelinating leukodystrophy	H00679	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ペリツェウス・メルツバッヘル病	Hypomyelinating leukodystrophy	https://identifiers.org/kegg.disease:H00679
NANDO:2200836	http://nanbyodata.jp/ontology/NANDO_2200836	先天性大脳白質形成不全症	Congenital hypomyelinating leukodystrophy	H00679	http://www.geneontology.org/formats/oboInOwl#hasDbXref	先天性大脳白質形成不全症	Pelizaeus-Merzbacher disease (PMD)	https://identifiers.org/kegg.disease:H00679
NANDO:2200836	http://nanbyodata.jp/ontology/NANDO_2200836	先天性大脳白質形成不全症	Congenital hypomyelinating leukodystrophy	H00679	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ペリツェウス・メルツバッヘル病	Pelizaeus-Merzbacher disease (PMD)	https://identifiers.org/kegg.disease:H00679
NANDO:2200837	http://nanbyodata.jp/ontology/NANDO_2200837	皮質下嚢胞をもつ大頭型白質脳症	Megaloencephalic leukoencephalopathy with subcortical cysts	H00875	http://www.geneontology.org/formats/oboInOwl#hasDbXref	皮質下嚢胞をもつ大頭型白質脳症	Megaloencephalic leukoencephalopathy with subcortical cysts	https://identifiers.org/kegg.disease:H00875
NANDO:2200838	http://nanbyodata.jp/ontology/NANDO_2200838	白質消失症	Vanishing white matter disease	H00869	http://www.geneontology.org/formats/oboInOwl#hasDbXref	白質消失病	Vanishing white matter disease	https://identifiers.org/kegg.disease:H00869
NANDO:2200838	http://nanbyodata.jp/ontology/NANDO_2200838	白質消失症	Vanishing white matter disease	H00869	http://www.geneontology.org/formats/oboInOwl#hasDbXref	Cree 白質脳症	Vanishing white matter disease	https://identifiers.org/kegg.disease:H00869
NANDO:2200838	http://nanbyodata.jp/ontology/NANDO_2200838	白質消失症	Vanishing white matter disease	H00869	http://www.geneontology.org/formats/oboInOwl#hasDbXref	VWM 型白質脳症	Vanishing white matter disease	https://identifiers.org/kegg.disease:H00869
NANDO:2200838	http://nanbyodata.jp/ontology/NANDO_2200838	白質消失症	Vanishing white matter disease	H00869	http://www.geneontology.org/formats/oboInOwl#hasDbXref	中枢神経系白質形成不全症を伴う小児失調症	Vanishing white matter disease	https://identifiers.org/kegg.disease:H00869
NANDO:2200838	http://nanbyodata.jp/ontology/NANDO_2200838	白質消失症	Vanishing white matter disease	H00869	http://www.geneontology.org/formats/oboInOwl#hasDbXref	白質消失病	Leukoencephalopathy with vanishing white matter	https://identifiers.org/kegg.disease:H00869
NANDO:2200838	http://nanbyodata.jp/ontology/NANDO_2200838	白質消失症	Vanishing white matter disease	H00869	http://www.geneontology.org/formats/oboInOwl#hasDbXref	Cree 白質脳症	Leukoencephalopathy with vanishing white matter	https://identifiers.org/kegg.disease:H00869
NANDO:2200838	http://nanbyodata.jp/ontology/NANDO_2200838	白質消失症	Vanishing white matter disease	H00869	http://www.geneontology.org/formats/oboInOwl#hasDbXref	VWM 型白質脳症	Leukoencephalopathy with vanishing white matter	https://identifiers.org/kegg.disease:H00869
NANDO:2200838	http://nanbyodata.jp/ontology/NANDO_2200838	白質消失症	Vanishing white matter disease	H00869	http://www.geneontology.org/formats/oboInOwl#hasDbXref	中枢神経系白質形成不全症を伴う小児失調症	Leukoencephalopathy with vanishing white matter	https://identifiers.org/kegg.disease:H00869
NANDO:2200838	http://nanbyodata.jp/ontology/NANDO_2200838	白質消失症	Vanishing white matter disease	H00869	http://www.geneontology.org/formats/oboInOwl#hasDbXref	白質消失病	Cree leukoencephalopathy (CLE)	https://identifiers.org/kegg.disease:H00869
NANDO:2200838	http://nanbyodata.jp/ontology/NANDO_2200838	白質消失症	Vanishing white matter disease	H00869	http://www.geneontology.org/formats/oboInOwl#hasDbXref	Cree 白質脳症	Cree leukoencephalopathy (CLE)	https://identifiers.org/kegg.disease:H00869
NANDO:2200838	http://nanbyodata.jp/ontology/NANDO_2200838	白質消失症	Vanishing white matter disease	H00869	http://www.geneontology.org/formats/oboInOwl#hasDbXref	VWM 型白質脳症	Cree leukoencephalopathy (CLE)	https://identifiers.org/kegg.disease:H00869
NANDO:2200838	http://nanbyodata.jp/ontology/NANDO_2200838	白質消失症	Vanishing white matter disease	H00869	http://www.geneontology.org/formats/oboInOwl#hasDbXref	中枢神経系白質形成不全症を伴う小児失調症	Cree leukoencephalopathy (CLE)	https://identifiers.org/kegg.disease:H00869
NANDO:2200838	http://nanbyodata.jp/ontology/NANDO_2200838	白質消失症	Vanishing white matter disease	H00869	http://www.geneontology.org/formats/oboInOwl#hasDbXref	白質消失病	Childhood ataxia with diffuse central nervous system hypomyelination (CACH)	https://identifiers.org/kegg.disease:H00869
NANDO:2200838	http://nanbyodata.jp/ontology/NANDO_2200838	白質消失症	Vanishing white matter disease	H00869	http://www.geneontology.org/formats/oboInOwl#hasDbXref	Cree 白質脳症	Childhood ataxia with diffuse central nervous system hypomyelination (CACH)	https://identifiers.org/kegg.disease:H00869
NANDO:2200838	http://nanbyodata.jp/ontology/NANDO_2200838	白質消失症	Vanishing white matter disease	H00869	http://www.geneontology.org/formats/oboInOwl#hasDbXref	VWM 型白質脳症	Childhood ataxia with diffuse central nervous system hypomyelination (CACH)	https://identifiers.org/kegg.disease:H00869
NANDO:2200838	http://nanbyodata.jp/ontology/NANDO_2200838	白質消失症	Vanishing white matter disease	H00869	http://www.geneontology.org/formats/oboInOwl#hasDbXref	中枢神経系白質形成不全症を伴う小児失調症	Childhood ataxia with diffuse central nervous system hypomyelination (CACH)	https://identifiers.org/kegg.disease:H00869
NANDO:2200839	http://nanbyodata.jp/ontology/NANDO_2200839	ATR-X症候群	ATR-X syndrome	H01752	http://www.geneontology.org/formats/oboInOwl#hasDbXref	X連鎖アルファサラセミア精神遅滞症候群	ATR-X syndrome	https://identifiers.org/kegg.disease:H01752
NANDO:2200839	http://nanbyodata.jp/ontology/NANDO_2200839	ATR-X症候群	ATR-X syndrome	H01752	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ATR-X 症候群	ATR-X syndrome	https://identifiers.org/kegg.disease:H01752
NANDO:2200839	http://nanbyodata.jp/ontology/NANDO_2200839	ATR-X症候群	ATR-X syndrome	H01752	http://www.geneontology.org/formats/oboInOwl#hasDbXref	X連鎖アルファサラセミア精神遅滞症候群	X-linked alpha-thalassemia/mental retardation syndrome	https://identifiers.org/kegg.disease:H01752
NANDO:2200839	http://nanbyodata.jp/ontology/NANDO_2200839	ATR-X症候群	ATR-X syndrome	H01752	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ATR-X 症候群	X-linked alpha-thalassemia/mental retardation syndrome	https://identifiers.org/kegg.disease:H01752
NANDO:2200840	http://nanbyodata.jp/ontology/NANDO_2200840	脆弱Ｘ症候群	Fragile X syndrome	H00465	http://www.geneontology.org/formats/oboInOwl#hasDbXref	脆弱Ｘ症候群	Fragile X syndrome	https://identifiers.org/kegg.disease:H00465
NANDO:2200842	http://nanbyodata.jp/ontology/NANDO_2200842	脳クレアチン欠乏症候群	Cerebral creatine deficiency syndrome	H00849	http://www.geneontology.org/formats/oboInOwl#hasDbXref	脳クレアチン欠乏症候群	Cerebral creatine deficiency syndrome	https://identifiers.org/kegg.disease:H00849
NANDO:2200844	http://nanbyodata.jp/ontology/NANDO_2200844	アペール症候群	Apert syndrome	H01755	http://www.geneontology.org/formats/oboInOwl#hasDbXref	アペール症候群	Apert syndrome	https://identifiers.org/kegg.disease:H01755
NANDO:2200850	http://nanbyodata.jp/ontology/NANDO_2200850	もやもや病	Moyamoya disease	H01396	http://www.geneontology.org/formats/oboInOwl#hasDbXref	もやもや病	Moyamoya disease	https://identifiers.org/kegg.disease:H01396
NANDO:2200853	http://nanbyodata.jp/ontology/NANDO_2200853	脊髄性筋萎縮症	Spinal muscular atrophy	H00455	http://www.geneontology.org/formats/oboInOwl#hasDbXref	脊髄性筋萎縮症	Spinal muscular atrophy	https://identifiers.org/kegg.disease:H00455
NANDO:2200854	http://nanbyodata.jp/ontology/NANDO_2200854	先天性無痛無汗症	Congenital insensitivity to pain with anhidrosis	H01836	http://www.geneontology.org/formats/oboInOwl#hasDbXref	先天性無痛無汗症	Congenital pain insensitivity with anhidrosis	https://identifiers.org/kegg.disease:H01836
NANDO:2200855	http://nanbyodata.jp/ontology/NANDO_2200855	遺伝性運動感覚ニューロパチー	Hereditary Motor and Sensory Neuropathy	H00264	http://www.geneontology.org/formats/oboInOwl#hasDbXref	シャルコー・マリー・トゥース病	Charcot-Marie-Tooth disease	https://identifiers.org/kegg.disease:H00264
NANDO:2200855	http://nanbyodata.jp/ontology/NANDO_2200855	遺伝性運動感覚ニューロパチー	Hereditary Motor and Sensory Neuropathy	H00264	http://www.geneontology.org/formats/oboInOwl#hasDbXref	遺伝性運動感覚ニューロパチー	Charcot-Marie-Tooth disease	https://identifiers.org/kegg.disease:H00264
NANDO:2200855	http://nanbyodata.jp/ontology/NANDO_2200855	遺伝性運動感覚ニューロパチー	Hereditary Motor and Sensory Neuropathy	H00264	http://www.geneontology.org/formats/oboInOwl#hasDbXref	シャルコー・マリー・トゥース病	Hereditary motor and sensory neuropathy	https://identifiers.org/kegg.disease:H00264
NANDO:2200855	http://nanbyodata.jp/ontology/NANDO_2200855	遺伝性運動感覚ニューロパチー	Hereditary Motor and Sensory Neuropathy	H00264	http://www.geneontology.org/formats/oboInOwl#hasDbXref	遺伝性運動感覚ニューロパチー	Hereditary motor and sensory neuropathy	https://identifiers.org/kegg.disease:H00264
NANDO:2200857	http://nanbyodata.jp/ontology/NANDO_2200857	エメリー・ドレイフス型筋ジストロフィー	Emery-Dreifuss muscular dystrophy	H00563	http://www.geneontology.org/formats/oboInOwl#hasDbXref	エメリー・ドレフュス型筋ジストロフィー	Emery-Dreifuss muscular dystrophy	https://identifiers.org/kegg.disease:H00563
NANDO:2200858	http://nanbyodata.jp/ontology/NANDO_2200858	肢帯型筋ジストロフィー	Limb-girdle muscular dystrophy	H00593	http://www.geneontology.org/formats/oboInOwl#hasDbXref	肢帯型筋ジストロフィー	Limb-girdle muscular dystrophy	https://identifiers.org/kegg.disease:H00593
NANDO:2200859	http://nanbyodata.jp/ontology/NANDO_2200859	顔面肩甲上腕型筋ジストロフィー	Facioscapulohumeral muscular dystrophy	H00591	http://www.geneontology.org/formats/oboInOwl#hasDbXref	顔面肩甲上腕型筋ジストロフィー	Facioscapulohumeral muscular dystrophy	https://identifiers.org/kegg.disease:H00591
NANDO:2200862	http://nanbyodata.jp/ontology/NANDO_2200862	ウルリヒ型先天性筋ジストロフィー	Ullrich congenital muscular dystrophy	H01778	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ウルリッヒ型先天性筋ジストロフィー	Ullrich congenital muscular dystrophy	https://identifiers.org/kegg.disease:H01778
NANDO:2200862	http://nanbyodata.jp/ontology/NANDO_2200862	ウルリヒ型先天性筋ジストロフィー	Ullrich congenital muscular dystrophy	H01778	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ウルリッヒ病	Ullrich congenital muscular dystrophy	https://identifiers.org/kegg.disease:H01778
NANDO:2200862	http://nanbyodata.jp/ontology/NANDO_2200862	ウルリヒ型先天性筋ジストロフィー	Ullrich congenital muscular dystrophy	H01778	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ウルリッヒ型先天性筋ジストロフィー	Ullrich disease	https://identifiers.org/kegg.disease:H01778
NANDO:2200862	http://nanbyodata.jp/ontology/NANDO_2200862	ウルリヒ型先天性筋ジストロフィー	Ullrich congenital muscular dystrophy	H01778	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ウルリッヒ病	Ullrich disease	https://identifiers.org/kegg.disease:H01778
NANDO:2200869	http://nanbyodata.jp/ontology/NANDO_2200869	ネマリンミオパチー	Nemaline myopathy	H00698	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ネマリンミオパチー	Nemaline myopathy	https://identifiers.org/kegg.disease:H00698
NANDO:2200870	http://nanbyodata.jp/ontology/NANDO_2200870	セントラルコア病	Central core disease	H00699	http://www.geneontology.org/formats/oboInOwl#hasDbXref	セントラルコア病	Central core disease	https://identifiers.org/kegg.disease:H00699
NANDO:2200876	http://nanbyodata.jp/ontology/NANDO_2200876	シュワルツ・ヤンペル症候群	Schwartz-Jampel syndrome	H01777	http://www.geneontology.org/formats/oboInOwl#hasDbXref	シュワルツ・ヤンペル症候群	Schwartz-Jampel syndrome	https://identifiers.org/kegg.disease:H01777
NANDO:2200878	http://nanbyodata.jp/ontology/NANDO_2200878	点頭てんかん	West syndrome	H01460	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ウエスト症候群	Infantile spasms	https://identifiers.org/kegg.disease:H01460
NANDO:2200878	http://nanbyodata.jp/ontology/NANDO_2200878	点頭てんかん	West syndrome	H01460	http://www.geneontology.org/formats/oboInOwl#hasDbXref	点頭てんかん	Infantile spasms	https://identifiers.org/kegg.disease:H01460
NANDO:2200878	http://nanbyodata.jp/ontology/NANDO_2200878	点頭てんかん	West syndrome	H01460	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ウエスト症候群	West syndrome	https://identifiers.org/kegg.disease:H01460
NANDO:2200878	http://nanbyodata.jp/ontology/NANDO_2200878	点頭てんかん	West syndrome	H01460	http://www.geneontology.org/formats/oboInOwl#hasDbXref	点頭てんかん	West syndrome	https://identifiers.org/kegg.disease:H01460
NANDO:2200879	http://nanbyodata.jp/ontology/NANDO_2200879	レノックス・ガストー症候群	Lennox-Gastaut syndrome	H01813	http://www.geneontology.org/formats/oboInOwl#hasDbXref	レノックス・ガストー症候群	Lennox-Gastaut syndrome	https://identifiers.org/kegg.disease:H01813
NANDO:2200882	http://nanbyodata.jp/ontology/NANDO_2200882	脊髄小脳変性症	spinocerebellar degeneration	H01616	http://www.geneontology.org/formats/oboInOwl#hasDbXref	脊髄小脳変性症	Spinocerebellar degeneration	https://identifiers.org/kegg.disease:H01616
NANDO:2200883	http://nanbyodata.jp/ontology/NANDO_2200883	小児交互性片麻痺	Alternating hemiplegia of childhood	H00998	http://www.geneontology.org/formats/oboInOwl#hasDbXref	小児交互性片麻痺	Alternating hemiplegia of childhood	https://identifiers.org/kegg.disease:H00998
NANDO:2200888	http://nanbyodata.jp/ontology/NANDO_2200888	乳児両側線条体壊死	Infantile bilateral striatal necrosis	H01177	http://www.geneontology.org/formats/oboInOwl#hasDbXref	乳児両側性線条体壊死	Infantile bilateral striatal necrosis	https://identifiers.org/kegg.disease:H01177
NANDO:2200893	http://nanbyodata.jp/ontology/NANDO_2200893	エカルディ・グティエール症候群	Aicardi-Goutières Syndrome	H00290	http://www.geneontology.org/formats/oboInOwl#hasDbXref	エカルディ・グティエール症候群	Aicardi-Goutieres syndrome	https://identifiers.org/kegg.disease:H00290
NANDO:2200899	http://nanbyodata.jp/ontology/NANDO_2200899	亜急性硬化性全脳炎	Subacute sclerosing panencephalitis	H01696	http://www.geneontology.org/formats/oboInOwl#hasDbXref	亜急性硬化性全脳炎	Subacute sclerosing panencephalitis	https://identifiers.org/kegg.disease:H01696
NANDO:2200900	http://nanbyodata.jp/ontology/NANDO_2200900	ラスムッセン脳炎	Rasmussen's encephalitis	H01812	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ラスムッセン脳炎	Rasmussen encephalitis	https://identifiers.org/kegg.disease:H01812
NANDO:2200900	http://nanbyodata.jp/ontology/NANDO_2200900	ラスムッセン脳炎	Rasmussen's encephalitis	H01812	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ラスムッセン症候群	Rasmussen encephalitis	https://identifiers.org/kegg.disease:H01812
NANDO:2200900	http://nanbyodata.jp/ontology/NANDO_2200900	ラスムッセン脳炎	Rasmussen's encephalitis	H01812	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ラスムッセン脳炎	Rasmussen syndrome	https://identifiers.org/kegg.disease:H01812
NANDO:2200900	http://nanbyodata.jp/ontology/NANDO_2200900	ラスムッセン脳炎	Rasmussen's encephalitis	H01812	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ラスムッセン症候群	Rasmussen syndrome	https://identifiers.org/kegg.disease:H01812
NANDO:2200901	http://nanbyodata.jp/ontology/NANDO_2200901	痙攣重積型急性脳症	Acute encephalopathy with biphasic seizures and late reduced diffusion	H01841	http://www.geneontology.org/formats/oboInOwl#hasDbXref	痙攣重積型 (二相性) 急性脳症	Acute encephalopathy with biphasic seizures and late reduced diffusion	https://identifiers.org/kegg.disease:H01841
NANDO:2200903	http://nanbyodata.jp/ontology/NANDO_2200903	難治頻回部分発作重積型急性脳炎	Acute encephalitis with refractory, repetitive partial seizures	H01829	http://www.geneontology.org/formats/oboInOwl#hasDbXref	難治頻回部分発作重積型急性脳炎	Acute encephalitis with refractory repetitive partial seizures	https://identifiers.org/kegg.disease:H01829
NANDO:2200904	http://nanbyodata.jp/ontology/NANDO_2200904	多発性硬化症	Multiple sclerosis	H01490	http://www.geneontology.org/formats/oboInOwl#hasDbXref	多発性硬化症	Multiple sclerosis	https://identifiers.org/kegg.disease:H01490
NANDO:2200905	http://nanbyodata.jp/ontology/NANDO_2200905	慢性炎症性脱髄性多発神経炎	Chronic inflammatory demyelinating polyneuropathy	H01527	http://www.geneontology.org/formats/oboInOwl#hasDbXref	多巣性運動ニューロパチー	Chronic inflammatory demyelinating polyradiculoneuropathy	https://identifiers.org/kegg.disease:H01527
NANDO:2200905	http://nanbyodata.jp/ontology/NANDO_2200905	慢性炎症性脱髄性多発神経炎	Chronic inflammatory demyelinating polyneuropathy	H01527	http://www.geneontology.org/formats/oboInOwl#hasDbXref	慢性炎症性脱髄性多発神経炎	Chronic inflammatory demyelinating polyradiculoneuropathy	https://identifiers.org/kegg.disease:H01527
NANDO:2200906	http://nanbyodata.jp/ontology/NANDO_2200906	重症筋無力症	Myasthenia gravis	H01594	http://www.geneontology.org/formats/oboInOwl#hasDbXref	重症筋無力症	Myasthenia gravis	https://identifiers.org/kegg.disease:H01594
NANDO:2200907	http://nanbyodata.jp/ontology/NANDO_2200907	乳糖不耐症	Lactose intolerance	H00116	http://www.geneontology.org/formats/oboInOwl#hasDbXref	乳糖不耐症	Congenital lactase deficiency	https://identifiers.org/kegg.disease:H00116
NANDO:2200907	http://nanbyodata.jp/ontology/NANDO_2200907	乳糖不耐症	Lactose intolerance	H00116	http://www.geneontology.org/formats/oboInOwl#hasDbXref	先天性ラクターゼ欠損症	Congenital lactase deficiency	https://identifiers.org/kegg.disease:H00116
NANDO:2200907	http://nanbyodata.jp/ontology/NANDO_2200907	乳糖不耐症	Lactose intolerance	H00116	http://www.geneontology.org/formats/oboInOwl#hasDbXref	II 型二糖類不耐症	Congenital lactase deficiency	https://identifiers.org/kegg.disease:H00116
NANDO:2200907	http://nanbyodata.jp/ontology/NANDO_2200907	乳糖不耐症	Lactose intolerance	H00116	http://www.geneontology.org/formats/oboInOwl#hasDbXref	乳糖不耐症	Disaccharide intolerance II	https://identifiers.org/kegg.disease:H00116
NANDO:2200907	http://nanbyodata.jp/ontology/NANDO_2200907	乳糖不耐症	Lactose intolerance	H00116	http://www.geneontology.org/formats/oboInOwl#hasDbXref	先天性ラクターゼ欠損症	Disaccharide intolerance II	https://identifiers.org/kegg.disease:H00116
NANDO:2200907	http://nanbyodata.jp/ontology/NANDO_2200907	乳糖不耐症	Lactose intolerance	H00116	http://www.geneontology.org/formats/oboInOwl#hasDbXref	II 型二糖類不耐症	Disaccharide intolerance II	https://identifiers.org/kegg.disease:H00116
NANDO:2200910	http://nanbyodata.jp/ontology/NANDO_2200910	エンテロキナーゼ欠損症	Enterokinase deficiency	H00988	http://www.geneontology.org/formats/oboInOwl#hasDbXref	エンテロキナーゼ欠損症	Enterokinase deficiency	https://identifiers.org/kegg.disease:H00988
NANDO:2200910	http://nanbyodata.jp/ontology/NANDO_2200910	エンテロキナーゼ欠損症	Enterokinase deficiency	H00988	http://www.geneontology.org/formats/oboInOwl#hasDbXref	エンテロペプチダーゼ欠損症	Enterokinase deficiency	https://identifiers.org/kegg.disease:H00988
NANDO:2200910	http://nanbyodata.jp/ontology/NANDO_2200910	エンテロキナーゼ欠損症	Enterokinase deficiency	H00988	http://www.geneontology.org/formats/oboInOwl#hasDbXref	エンテロキナーゼ欠損症	Enteropeptidase deficiency	https://identifiers.org/kegg.disease:H00988
NANDO:2200910	http://nanbyodata.jp/ontology/NANDO_2200910	エンテロキナーゼ欠損症	Enterokinase deficiency	H00988	http://www.geneontology.org/formats/oboInOwl#hasDbXref	エンテロペプチダーゼ欠損症	Enteropeptidase deficiency	https://identifiers.org/kegg.disease:H00988
NANDO:2200917	http://nanbyodata.jp/ontology/NANDO_2200917	ポイツ・ジェガース症候群	Peutz-Jeghers syndrome	H00666	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ポイツ・ジェーガーズ症候群	Peutz-Jeghers syndrome	https://identifiers.org/kegg.disease:H00666
NANDO:2200918	http://nanbyodata.jp/ontology/NANDO_2200918	カウデン症候群	Cowden syndrome	H01222	http://www.geneontology.org/formats/oboInOwl#hasDbXref	カウデン症候群	Cowden syndrome	https://identifiers.org/kegg.disease:H01222
NANDO:2200920	http://nanbyodata.jp/ontology/NANDO_2200920	潰瘍性大腸炎	Ulcerative colitis	H01466	http://www.geneontology.org/formats/oboInOwl#hasDbXref	潰瘍性大腸炎	Ulcerative colitis	https://identifiers.org/kegg.disease:H01466
NANDO:2200921	http://nanbyodata.jp/ontology/NANDO_2200921	クローン病	Crohn's disease	H00286	http://www.geneontology.org/formats/oboInOwl#hasDbXref	クローン病	Crohn disease	https://identifiers.org/kegg.disease:H00286
NANDO:2200925	http://nanbyodata.jp/ontology/NANDO_2200925	非特異性多発性小腸潰瘍症	Chronic nonspecific multiple ulcers of the small intestine	H01853	http://www.geneontology.org/formats/oboInOwl#hasDbXref	非特異性多発性小腸潰瘍症	Chronic nonspecific multiple ulcers of the small intestine	https://identifiers.org/kegg.disease:H01853
NANDO:2200928	http://nanbyodata.jp/ontology/NANDO_2200928	自己免疫性肝炎	Autoimmune hepatitis	H01685	http://www.geneontology.org/formats/oboInOwl#hasDbXref	自己免疫性肝炎	Autoimmune hepatitis	https://identifiers.org/kegg.disease:H01685
NANDO:2200929	http://nanbyodata.jp/ontology/NANDO_2200929	原発性硬化性胆管炎	Primary sclerosing cholangitis	H01684	http://www.geneontology.org/formats/oboInOwl#hasDbXref	原発性硬化性胆管炎	Primary sclerosing cholangitis	https://identifiers.org/kegg.disease:H01684
NANDO:2200930	http://nanbyodata.jp/ontology/NANDO_2200930	胆道閉鎖症	biliary atresia	H01855	http://www.geneontology.org/formats/oboInOwl#hasDbXref	胆道閉鎖症	Biliary atresia	https://identifiers.org/kegg.disease:H01855
NANDO:2200931	http://nanbyodata.jp/ontology/NANDO_2200931	アラジール症候群	Alagille syndrome	H00551	http://www.geneontology.org/formats/oboInOwl#hasDbXref	アラジール症候群	Alagille syndrome	https://identifiers.org/kegg.disease:H00551
NANDO:2200933	http://nanbyodata.jp/ontology/NANDO_2200933	進行性家族性肝内胆汁うっ滞症	Progressive familial intrahepatic cholestasis	H00624	http://www.geneontology.org/formats/oboInOwl#hasDbXref	進行性家族性肝内胆汁うっ滞症	Progressive familial intrahepatic cholestasis	https://identifiers.org/kegg.disease:H00624
NANDO:2200942	http://nanbyodata.jp/ontology/NANDO_2200942	遺伝性膵炎	Hereditary pancreatitis	H00933	http://www.geneontology.org/formats/oboInOwl#hasDbXref	遺伝性膵炎	Hereditary pancreatitis	https://identifiers.org/kegg.disease:H00933
NANDO:2200942	http://nanbyodata.jp/ontology/NANDO_2200942	遺伝性膵炎	Hereditary pancreatitis	H00933	http://www.geneontology.org/formats/oboInOwl#hasDbXref	遺伝性膵炎	Hereditary chronic pancreatitis	https://identifiers.org/kegg.disease:H00933
NANDO:2200944	http://nanbyodata.jp/ontology/NANDO_2200944	短腸症	Short bowel syndrome	H01469	http://www.geneontology.org/formats/oboInOwl#hasDbXref	短腸症候群	Short bowel syndrome	https://identifiers.org/kegg.disease:H01469
NANDO:2200945	http://nanbyodata.jp/ontology/NANDO_2200945	ヒルシュスプルング病	Hirschsprung disease	H00910	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ヒルシュスプルング病	Hirschsprung disease	https://identifiers.org/kegg.disease:H00910
NANDO:2200946	http://nanbyodata.jp/ontology/NANDO_2200946	慢性特発性偽性腸閉塞症	Chronic idiopathic intestinal pseudo-obstruction	H01276	http://www.geneontology.org/formats/oboInOwl#hasDbXref	慢性特発性偽性腸閉塞症	CIIP	https://identifiers.org/kegg.disease:H01276
NANDO:2200946	http://nanbyodata.jp/ontology/NANDO_2200946	慢性特発性偽性腸閉塞症	Chronic idiopathic intestinal pseudo-obstruction	H01276	http://www.geneontology.org/formats/oboInOwl#hasDbXref	慢性特発性偽性腸閉塞症	Chronic idiopathic intestinal pseudo-obstruction	https://identifiers.org/kegg.disease:H01276
NANDO:2200951	http://nanbyodata.jp/ontology/NANDO_2200951	総排泄腔外反症	Cloacal exstrophy	H01856	http://www.geneontology.org/formats/oboInOwl#hasDbXref	総排泄腔外反症	Cloacal exstrophy	https://identifiers.org/kegg.disease:H01856
NANDO:2200951	http://nanbyodata.jp/ontology/NANDO_2200951	総排泄腔外反症	Cloacal exstrophy	H01856	http://www.geneontology.org/formats/oboInOwl#hasDbXref	膀胱腸裂	Cloacal exstrophy	https://identifiers.org/kegg.disease:H01856
NANDO:2200951	http://nanbyodata.jp/ontology/NANDO_2200951	総排泄腔外反症	Cloacal exstrophy	H01856	http://www.geneontology.org/formats/oboInOwl#hasDbXref	総排泄腔外反症	Vesicointestinal fissure	https://identifiers.org/kegg.disease:H01856
NANDO:2200951	http://nanbyodata.jp/ontology/NANDO_2200951	総排泄腔外反症	Cloacal exstrophy	H01856	http://www.geneontology.org/formats/oboInOwl#hasDbXref	膀胱腸裂	Vesicointestinal fissure	https://identifiers.org/kegg.disease:H01856
NANDO:2200952	http://nanbyodata.jp/ontology/NANDO_2200952	コフィン・ローリー症候群	Coffin-Lowry syndrome	H00574	http://www.geneontology.org/formats/oboInOwl#hasDbXref	コフィン・ローリー症候群	Coffin-Lowry syndrome	https://identifiers.org/kegg.disease:H00574
NANDO:2200953	http://nanbyodata.jp/ontology/NANDO_2200953	ソトス症候群	Sotos syndrome	H00718	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ソトス症候群	Sotos syndrome	https://identifiers.org/kegg.disease:H00718
NANDO:2200954	http://nanbyodata.jp/ontology/NANDO_2200954	スミス・マギニス症候群	Smith-Magenis syndrome	H01791	http://www.geneontology.org/formats/oboInOwl#hasDbXref	スミス・マギニス症候群	Smith-Magenis syndrome	https://identifiers.org/kegg.disease:H01791
NANDO:2200955	http://nanbyodata.jp/ontology/NANDO_2200955	ルビンシュタイン・テイビ症候群	Rubinstein-Taybi syndrome	H00504	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ルビンシュタイン・テイビ症候群	Rubinstein-Taybi syndrome	https://identifiers.org/kegg.disease:H00504
NANDO:2200956	http://nanbyodata.jp/ontology/NANDO_2200956	歌舞伎症候群	Kabuki syndrome	H00570	http://www.geneontology.org/formats/oboInOwl#hasDbXref	歌舞伎症候群	Kabuki syndrome	https://identifiers.org/kegg.disease:H00570
NANDO:2200957	http://nanbyodata.jp/ontology/NANDO_2200957	ウィーバー症候群	Weaver syndrome	H01751	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ウィーバー症候群	Weaver syndrome	https://identifiers.org/kegg.disease:H01751
NANDO:2200958	http://nanbyodata.jp/ontology/NANDO_2200958	コルネリア・デランゲ症候群	Cornelia de Lange syndrome	H00631	http://www.geneontology.org/formats/oboInOwl#hasDbXref	コルネリア・デランゲ症候群	Cornelia de Lange syndrome	https://identifiers.org/kegg.disease:H00631
NANDO:2200959	http://nanbyodata.jp/ontology/NANDO_2200959	ベックウィズ・ヴィーデマン症候群	Beckwith-Wiedemann syndrome	H00713	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ベックウィズ・ウイーデマン症候群	Beckwith-Wiedemann syndrome	https://identifiers.org/kegg.disease:H00713
NANDO:2200960	http://nanbyodata.jp/ontology/NANDO_2200960	アンジェルマン症候群	Angelman syndrome	H01732	http://www.geneontology.org/formats/oboInOwl#hasDbXref	アンジェルマン症候群	Angelman syndrome	https://identifiers.org/kegg.disease:H01732
NANDO:2200965	http://nanbyodata.jp/ontology/NANDO_2200965	ダウン症候群	Down syndrome	H01552	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ダウン症候群	Down syndrome	https://identifiers.org/kegg.disease:H01552
NANDO:2200965	http://nanbyodata.jp/ontology/NANDO_2200965	ダウン症候群	Down syndrome	H01552	http://www.geneontology.org/formats/oboInOwl#hasDbXref	21 トリソミー	Down syndrome	https://identifiers.org/kegg.disease:H01552
NANDO:2200965	http://nanbyodata.jp/ontology/NANDO_2200965	ダウン症候群	Down syndrome	H01552	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ダウン症候群	Trisomy 21	https://identifiers.org/kegg.disease:H01552
NANDO:2200965	http://nanbyodata.jp/ontology/NANDO_2200965	ダウン症候群	Down syndrome	H01552	http://www.geneontology.org/formats/oboInOwl#hasDbXref	21 トリソミー	Trisomy 21	https://identifiers.org/kegg.disease:H01552
NANDO:2200968	http://nanbyodata.jp/ontology/NANDO_2200968	マルファン症候群	Marfan syndrome	H00653	http://www.geneontology.org/formats/oboInOwl#hasDbXref	マルファン症候群	Marfan syndrome	https://identifiers.org/kegg.disease:H00653
NANDO:2200969	http://nanbyodata.jp/ontology/NANDO_2200969	ロイス・ディーツ症候群	Loeys-Dietz syndrome	H00800	http://www.geneontology.org/formats/oboInOwl#hasDbXref	Loeys-Dietz 症候群	Loeys-Dietz syndrome	https://identifiers.org/kegg.disease:H00800
NANDO:2200970	http://nanbyodata.jp/ontology/NANDO_2200970	カムラティ・エンゲルマン症候群	Camurati-Engelmann disease	H00434	http://www.geneontology.org/formats/oboInOwl#hasDbXref	Camurati-Engelmann病	Camurati-Engelmann disease	https://identifiers.org/kegg.disease:H00434
NANDO:2200970	http://nanbyodata.jp/ontology/NANDO_2200970	カムラティ・エンゲルマン症候群	Camurati-Engelmann disease	H00434	http://www.geneontology.org/formats/oboInOwl#hasDbXref	進行性骨幹異形成症	Camurati-Engelmann disease	https://identifiers.org/kegg.disease:H00434
NANDO:2200970	http://nanbyodata.jp/ontology/NANDO_2200970	カムラティ・エンゲルマン症候群	Camurati-Engelmann disease	H00434	http://www.geneontology.org/formats/oboInOwl#hasDbXref	Camurati-Engelmann病	Progressive diaphyseal dysplasia	https://identifiers.org/kegg.disease:H00434
NANDO:2200970	http://nanbyodata.jp/ontology/NANDO_2200970	カムラティ・エンゲルマン症候群	Camurati-Engelmann disease	H00434	http://www.geneontology.org/formats/oboInOwl#hasDbXref	進行性骨幹異形成症	Progressive diaphyseal dysplasia	https://identifiers.org/kegg.disease:H00434
NANDO:2200971	http://nanbyodata.jp/ontology/NANDO_2200971	コステロ症候群	Costello syndrome	H01747	http://www.geneontology.org/formats/oboInOwl#hasDbXref	コステロ症候群	Costello syndrome	https://identifiers.org/kegg.disease:H01747
NANDO:2200972	http://nanbyodata.jp/ontology/NANDO_2200972	チャージ症候群	CHARGE syndrome	H00556	http://www.geneontology.org/formats/oboInOwl#hasDbXref	チャージ症候群	CHARGE syndrome	https://identifiers.org/kegg.disease:H00556
NANDO:2200974	http://nanbyodata.jp/ontology/NANDO_2200974	色素失調症	Incontinentia pigmenti	H00645	http://www.geneontology.org/formats/oboInOwl#hasDbXref	色素失調症	Incontinentia pigmenti	https://identifiers.org/kegg.disease:H00645
NANDO:2200975	http://nanbyodata.jp/ontology/NANDO_2200975	アントレー・ビクスラー症候群	Antley-Bixler syndrome	H01753	http://www.geneontology.org/formats/oboInOwl#hasDbXref	アントレー・ビクスラー症候群	Antley-Bixler syndrome	https://identifiers.org/kegg.disease:H01753
NANDO:2200976	http://nanbyodata.jp/ontology/NANDO_2200976	ファイファー症候群	Pfeiffer syndrome	H01756	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ファイファー症候群	Pfeiffer syndrome	https://identifiers.org/kegg.disease:H01756
NANDO:2200977	http://nanbyodata.jp/ontology/NANDO_2200977	コフィン・シリス症候群	Coffin-Siris syndrome	H01403	http://www.geneontology.org/formats/oboInOwl#hasDbXref	コフィン・シリス症候群	Coffin-Siris syndrome	https://identifiers.org/kegg.disease:H01403
NANDO:2200978	http://nanbyodata.jp/ontology/NANDO_2200978	シンプソン・ゴラビ・ベーメル症候群	Simpson-Golabi-Behmel syndrome	H01215	http://www.geneontology.org/formats/oboInOwl#hasDbXref	Simpson-Golabi-Behmel 症候群	Simpson-Golabi-Behmel syndrome	https://identifiers.org/kegg.disease:H01215
NANDO:2200979	http://nanbyodata.jp/ontology/NANDO_2200979	スミス・レムリ・オピッツ症候群	Smith-Lemli-Opitz syndrome	H00161	http://www.geneontology.org/formats/oboInOwl#hasDbXref	スミス・レムリ・オピッツ症候群	Smith-Lemli-Opitz syndrome	https://identifiers.org/kegg.disease:H00161
NANDO:2200980	http://nanbyodata.jp/ontology/NANDO_2200980	メビウス症候群	Moebius syndrome	H01840	http://www.geneontology.org/formats/oboInOwl#hasDbXref	メビウス症候群	Moebius syndrome	https://identifiers.org/kegg.disease:H01840
NANDO:2200980	http://nanbyodata.jp/ontology/NANDO_2200980	メビウス症候群	Moebius syndrome	H01840	http://www.geneontology.org/formats/oboInOwl#hasDbXref	メビウス症候群	Mobius syndrome	https://identifiers.org/kegg.disease:H01840
NANDO:2200981	http://nanbyodata.jp/ontology/NANDO_2200981	モワット・ウィルソン症候群	Mowat-Wilson syndrome	H00908	http://www.geneontology.org/formats/oboInOwl#hasDbXref	モワットウィルソン症候群	Mowat-Wilson syndrome	https://identifiers.org/kegg.disease:H00908
NANDO:2200982	http://nanbyodata.jp/ontology/NANDO_2200982	ヤング・シンプソン症候群	Young-Simpson syndrome	H01793	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ヤング・シンプソン症候群	Young-Simpson syndrome	https://identifiers.org/kegg.disease:H01793
NANDO:2200982	http://nanbyodata.jp/ontology/NANDO_2200982	ヤング・シンプソン症候群	Young-Simpson syndrome	H01793	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ヤング・シンプソン症候群	Say-Barber-Biesecker-Young-Simpson syndrome	https://identifiers.org/kegg.disease:H01793
NANDO:2200982	http://nanbyodata.jp/ontology/NANDO_2200982	ヤング・シンプソン症候群	Young-Simpson syndrome	H01793	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ヤング・シンプソン症候群	Say-Barber-Biesecker variant of Ohdo syndrome	https://identifiers.org/kegg.disease:H01793
NANDO:2200986	http://nanbyodata.jp/ontology/NANDO_2200986	眼皮膚白皮症	Oculocutaneous albinism	H00168	http://www.geneontology.org/formats/oboInOwl#hasDbXref	眼皮膚白皮症	Oculocutaneous albinism	https://identifiers.org/kegg.disease:H00168
NANDO:2200991	http://nanbyodata.jp/ontology/NANDO_2200991	常染色体劣性遺伝性魚鱗癬	Autosomal recessive congenital ichthyosis	H00734	http://www.geneontology.org/formats/oboInOwl#hasDbXref	常染色体劣性遺伝性先天性魚鱗癬	Autosomal recessive congenital ichthyosis	https://identifiers.org/kegg.disease:H00734
NANDO:2200992	http://nanbyodata.jp/ontology/NANDO_2200992	道化師様魚鱗癬	Harlequin ichthyosis	H00733	http://www.geneontology.org/formats/oboInOwl#hasDbXref	道化師様魚鱗癬	Harlequin ichthyosis	https://identifiers.org/kegg.disease:H00733
NANDO:2200993	http://nanbyodata.jp/ontology/NANDO_2200993	ネザートン症候群	Netherton syndrome	H00671	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ネザートン症候群	Netherton syndrome	https://identifiers.org/kegg.disease:H00671
NANDO:2200994	http://nanbyodata.jp/ontology/NANDO_2200994	シェーグレン・ラルソン症候群	Sjögren-Larsson syndrome	H00162	http://www.geneontology.org/formats/oboInOwl#hasDbXref	シェーグレン・ラルソン症候群	Sjogren-Larsson syndrome	https://identifiers.org/kegg.disease:H00162
NANDO:2200997	http://nanbyodata.jp/ontology/NANDO_2200997	ドルフマン・シャナリン症候群	Dorfman-Chanarin syndrome	H00736	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ドルフマン・シャナリン症候群	Dorfman-Chanarin syndrome	https://identifiers.org/kegg.disease:H00736
NANDO:2200997	http://nanbyodata.jp/ontology/NANDO_2200997	ドルフマン・シャナリン症候群	Dorfman-Chanarin syndrome	H00736	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ドルフマン・シャナリン症候群	Chanarin-Dorfman syndrome	https://identifiers.org/kegg.disease:H00736
NANDO:2201000	http://nanbyodata.jp/ontology/NANDO_2201000	表皮水疱症	Epidermolysis bullosa	H01737	http://www.geneontology.org/formats/oboInOwl#hasDbXref	表皮水疱症	Epidermolysis bullosa	https://identifiers.org/kegg.disease:H01737
NANDO:2201001	http://nanbyodata.jp/ontology/NANDO_2201001	膿疱性乾癬（汎発型）	Pustular psoriasis	H01663	http://www.geneontology.org/formats/oboInOwl#hasDbXref	膿疱性乾癬	Pustular psoriasis	https://identifiers.org/kegg.disease:H01663
NANDO:2201002	http://nanbyodata.jp/ontology/NANDO_2201002	色素性乾皮症	Xeroderma pigmentosum	H01428	http://www.geneontology.org/formats/oboInOwl#hasDbXref	色素性乾皮症	Xeroderma pigmentosum	https://identifiers.org/kegg.disease:H01428
NANDO:2201003	http://nanbyodata.jp/ontology/NANDO_2201003	レックリングハウゼン病	von Recklinghausen's disease	H01437	http://www.geneontology.org/formats/oboInOwl#hasDbXref	レックリングハウゼン病	Neurofibromatosis type 1	https://identifiers.org/kegg.disease:H01437
NANDO:2201003	http://nanbyodata.jp/ontology/NANDO_2201003	レックリングハウゼン病	von Recklinghausen's disease	H01437	http://www.geneontology.org/formats/oboInOwl#hasDbXref	神経線維腫症 I 型	Neurofibromatosis type 1	https://identifiers.org/kegg.disease:H01437
NANDO:2201003	http://nanbyodata.jp/ontology/NANDO_2201003	レックリングハウゼン病	von Recklinghausen's disease	H01437	http://www.geneontology.org/formats/oboInOwl#hasDbXref	レックリングハウゼン病	Von Recklinghausen disease	https://identifiers.org/kegg.disease:H01437
NANDO:2201003	http://nanbyodata.jp/ontology/NANDO_2201003	レックリングハウゼン病	von Recklinghausen's disease	H01437	http://www.geneontology.org/formats/oboInOwl#hasDbXref	神経線維腫症 I 型	Von Recklinghausen disease	https://identifiers.org/kegg.disease:H01437
NANDO:2201006	http://nanbyodata.jp/ontology/NANDO_2201006	スティーヴンス・ジョンソン症候群	Stevens-Johnson syndrome	H01694	http://www.geneontology.org/formats/oboInOwl#hasDbXref	中毒性表皮壊死症	Stevens-Johnson syndrome	https://identifiers.org/kegg.disease:H01694
NANDO:2201006	http://nanbyodata.jp/ontology/NANDO_2201006	スティーヴンス・ジョンソン症候群	Stevens-Johnson syndrome	H01694	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ライエル症候群	Stevens-Johnson syndrome	https://identifiers.org/kegg.disease:H01694
NANDO:2201006	http://nanbyodata.jp/ontology/NANDO_2201006	スティーヴンス・ジョンソン症候群	Stevens-Johnson syndrome	H01694	http://www.geneontology.org/formats/oboInOwl#hasDbXref	スティーブンス・ジョンソン症候群	Stevens-Johnson syndrome	https://identifiers.org/kegg.disease:H01694
NANDO:2201006	http://nanbyodata.jp/ontology/NANDO_2201006	スティーヴンス・ジョンソン症候群	Stevens-Johnson syndrome	H01694	http://www.geneontology.org/formats/oboInOwl#hasDbXref	重症多形滲出性紅斑	Stevens-Johnson syndrome	https://identifiers.org/kegg.disease:H01694
NANDO:2201006	http://nanbyodata.jp/ontology/NANDO_2201006	スティーヴンス・ジョンソン症候群	Stevens-Johnson syndrome	H01694	http://www.geneontology.org/formats/oboInOwl#hasDbXref	中毒性表皮壊死症	Toxic epidermal necrolysis	https://identifiers.org/kegg.disease:H01694
NANDO:2201006	http://nanbyodata.jp/ontology/NANDO_2201006	スティーヴンス・ジョンソン症候群	Stevens-Johnson syndrome	H01694	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ライエル症候群	Toxic epidermal necrolysis	https://identifiers.org/kegg.disease:H01694
NANDO:2201006	http://nanbyodata.jp/ontology/NANDO_2201006	スティーヴンス・ジョンソン症候群	Stevens-Johnson syndrome	H01694	http://www.geneontology.org/formats/oboInOwl#hasDbXref	スティーブンス・ジョンソン症候群	Toxic epidermal necrolysis	https://identifiers.org/kegg.disease:H01694
NANDO:2201006	http://nanbyodata.jp/ontology/NANDO_2201006	スティーヴンス・ジョンソン症候群	Stevens-Johnson syndrome	H01694	http://www.geneontology.org/formats/oboInOwl#hasDbXref	重症多形滲出性紅斑	Toxic epidermal necrolysis	https://identifiers.org/kegg.disease:H01694
NANDO:2201006	http://nanbyodata.jp/ontology/NANDO_2201006	スティーヴンス・ジョンソン症候群	Stevens-Johnson syndrome	H01694	http://www.geneontology.org/formats/oboInOwl#hasDbXref	中毒性表皮壊死症	Lyell syndrome	https://identifiers.org/kegg.disease:H01694
NANDO:2201006	http://nanbyodata.jp/ontology/NANDO_2201006	スティーヴンス・ジョンソン症候群	Stevens-Johnson syndrome	H01694	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ライエル症候群	Lyell syndrome	https://identifiers.org/kegg.disease:H01694
NANDO:2201006	http://nanbyodata.jp/ontology/NANDO_2201006	スティーヴンス・ジョンソン症候群	Stevens-Johnson syndrome	H01694	http://www.geneontology.org/formats/oboInOwl#hasDbXref	スティーブンス・ジョンソン症候群	Lyell syndrome	https://identifiers.org/kegg.disease:H01694
NANDO:2201006	http://nanbyodata.jp/ontology/NANDO_2201006	スティーヴンス・ジョンソン症候群	Stevens-Johnson syndrome	H01694	http://www.geneontology.org/formats/oboInOwl#hasDbXref	重症多形滲出性紅斑	Lyell syndrome	https://identifiers.org/kegg.disease:H01694
NANDO:2201007	http://nanbyodata.jp/ontology/NANDO_2201007	中毒性表皮壊死症	Toxic epidermal necrolysis	H01694	http://www.geneontology.org/formats/oboInOwl#hasDbXref	中毒性表皮壊死症	Stevens-Johnson syndrome	https://identifiers.org/kegg.disease:H01694
NANDO:2201007	http://nanbyodata.jp/ontology/NANDO_2201007	中毒性表皮壊死症	Toxic epidermal necrolysis	H01694	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ライエル症候群	Stevens-Johnson syndrome	https://identifiers.org/kegg.disease:H01694
NANDO:2201007	http://nanbyodata.jp/ontology/NANDO_2201007	中毒性表皮壊死症	Toxic epidermal necrolysis	H01694	http://www.geneontology.org/formats/oboInOwl#hasDbXref	スティーブンス・ジョンソン症候群	Stevens-Johnson syndrome	https://identifiers.org/kegg.disease:H01694
NANDO:2201007	http://nanbyodata.jp/ontology/NANDO_2201007	中毒性表皮壊死症	Toxic epidermal necrolysis	H01694	http://www.geneontology.org/formats/oboInOwl#hasDbXref	重症多形滲出性紅斑	Stevens-Johnson syndrome	https://identifiers.org/kegg.disease:H01694
NANDO:2201007	http://nanbyodata.jp/ontology/NANDO_2201007	中毒性表皮壊死症	Toxic epidermal necrolysis	H01694	http://www.geneontology.org/formats/oboInOwl#hasDbXref	中毒性表皮壊死症	Toxic epidermal necrolysis	https://identifiers.org/kegg.disease:H01694
NANDO:2201007	http://nanbyodata.jp/ontology/NANDO_2201007	中毒性表皮壊死症	Toxic epidermal necrolysis	H01694	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ライエル症候群	Toxic epidermal necrolysis	https://identifiers.org/kegg.disease:H01694
NANDO:2201007	http://nanbyodata.jp/ontology/NANDO_2201007	中毒性表皮壊死症	Toxic epidermal necrolysis	H01694	http://www.geneontology.org/formats/oboInOwl#hasDbXref	スティーブンス・ジョンソン症候群	Toxic epidermal necrolysis	https://identifiers.org/kegg.disease:H01694
NANDO:2201007	http://nanbyodata.jp/ontology/NANDO_2201007	中毒性表皮壊死症	Toxic epidermal necrolysis	H01694	http://www.geneontology.org/formats/oboInOwl#hasDbXref	重症多形滲出性紅斑	Toxic epidermal necrolysis	https://identifiers.org/kegg.disease:H01694
NANDO:2201007	http://nanbyodata.jp/ontology/NANDO_2201007	中毒性表皮壊死症	Toxic epidermal necrolysis	H01694	http://www.geneontology.org/formats/oboInOwl#hasDbXref	中毒性表皮壊死症	Lyell syndrome	https://identifiers.org/kegg.disease:H01694
NANDO:2201007	http://nanbyodata.jp/ontology/NANDO_2201007	中毒性表皮壊死症	Toxic epidermal necrolysis	H01694	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ライエル症候群	Lyell syndrome	https://identifiers.org/kegg.disease:H01694
NANDO:2201007	http://nanbyodata.jp/ontology/NANDO_2201007	中毒性表皮壊死症	Toxic epidermal necrolysis	H01694	http://www.geneontology.org/formats/oboInOwl#hasDbXref	スティーブンス・ジョンソン症候群	Lyell syndrome	https://identifiers.org/kegg.disease:H01694
NANDO:2201007	http://nanbyodata.jp/ontology/NANDO_2201007	中毒性表皮壊死症	Toxic epidermal necrolysis	H01694	http://www.geneontology.org/formats/oboInOwl#hasDbXref	重症多形滲出性紅斑	Lyell syndrome	https://identifiers.org/kegg.disease:H01694
NANDO:2201009	http://nanbyodata.jp/ontology/NANDO_2201009	軟骨無形成症	Achondroplasia	H01749	http://www.geneontology.org/formats/oboInOwl#hasDbXref	軟骨無形成症	Achondroplasia	https://identifiers.org/kegg.disease:H01749
NANDO:2201011	http://nanbyodata.jp/ontology/NANDO_2201011	骨形成不全症	Osteogenesis imperfecta	H00506	http://www.geneontology.org/formats/oboInOwl#hasDbXref	骨形成不全症	Osteogenesis imperfecta	https://identifiers.org/kegg.disease:H00506
NANDO:2201012	http://nanbyodata.jp/ontology/NANDO_2201012	低ホスファターゼ症	Hypophosphatasia	H00213	http://www.geneontology.org/formats/oboInOwl#hasDbXref	低ホスファターゼ症	Hypophosphatasia	https://identifiers.org/kegg.disease:H00213
NANDO:2201013	http://nanbyodata.jp/ontology/NANDO_2201013	大理石骨病	Osteopetrosis	H00436	http://www.geneontology.org/formats/oboInOwl#hasDbXref	大理石骨病	Osteopetrosis	https://identifiers.org/kegg.disease:H00436
NANDO:2201018	http://nanbyodata.jp/ontology/NANDO_2201018	偽性軟骨無形成症	Pseudoachondroplasia	H00477	http://www.geneontology.org/formats/oboInOwl#hasDbXref	偽軟骨異形成症	Pseudoachondroplasia	https://identifiers.org/kegg.disease:H00477
NANDO:2201020	http://nanbyodata.jp/ontology/NANDO_2201020	進行性骨化性線維異形成症	Fibrodysplasia ossificans progressiva	H00430	http://www.geneontology.org/formats/oboInOwl#hasDbXref	進行性骨化性線維異形成症	Fibrodysplasia ossificans progressiva	https://identifiers.org/kegg.disease:H00430
NANDO:2201020	http://nanbyodata.jp/ontology/NANDO_2201020	進行性骨化性線維異形成症	Fibrodysplasia ossificans progressiva	H00430	http://www.geneontology.org/formats/oboInOwl#hasDbXref	進行性骨化線維増殖症	Fibrodysplasia ossificans progressiva	https://identifiers.org/kegg.disease:H00430
NANDO:2201023	http://nanbyodata.jp/ontology/NANDO_2201023	濃化異骨症	Pycnodysostosis	H00273	http://www.geneontology.org/formats/oboInOwl#hasDbXref	濃化異骨症	Pycnodysostosis	https://identifiers.org/kegg.disease:H00273
NANDO:2201024	http://nanbyodata.jp/ontology/NANDO_2201024	骨斑紋症	Osteopoikilosis	H00452	http://www.geneontology.org/formats/oboInOwl#hasDbXref	骨斑紋症	Osteopoikilosis	https://identifiers.org/kegg.disease:H00452
NANDO:2201024	http://nanbyodata.jp/ontology/NANDO_2201024	骨斑紋症	Osteopoikilosis	H00452	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ブシュケ‐オレンドルフ症候群	Osteopoikilosis	https://identifiers.org/kegg.disease:H00452
NANDO:2201024	http://nanbyodata.jp/ontology/NANDO_2201024	骨斑紋症	Osteopoikilosis	H00452	http://www.geneontology.org/formats/oboInOwl#hasDbXref	骨斑紋症	Buschke-Ollendorff syndrome	https://identifiers.org/kegg.disease:H00452
NANDO:2201024	http://nanbyodata.jp/ontology/NANDO_2201024	骨斑紋症	Osteopoikilosis	H00452	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ブシュケ‐オレンドルフ症候群	Buschke-Ollendorff syndrome	https://identifiers.org/kegg.disease:H00452
NANDO:2201030	http://nanbyodata.jp/ontology/NANDO_2201030	クリッペル・トレノネー・ウェーバー症候群	Klippel-Trenaunay-Weber syndrome	H01788	http://www.geneontology.org/formats/oboInOwl#hasDbXref	クリッペル・トレノネー・ウェーバー症候群	Klippel-Trenaunay-Weber syndrome	https://identifiers.org/kegg.disease:H01788
NANDO:2201032	http://nanbyodata.jp/ontology/NANDO_2201032	リンパ管腫	Lymphangioma	H01471	http://www.geneontology.org/formats/oboInOwl#hasDbXref	リンパ管腫	Lymphangioma	https://identifiers.org/kegg.disease:H01471
NANDO:2201033	http://nanbyodata.jp/ontology/NANDO_2201033	リンパ管腫症	Lymphangiomatosis	H01735	http://www.geneontology.org/formats/oboInOwl#hasDbXref	リンパ管腫症	Lymphangiomatosis	https://identifiers.org/kegg.disease:H01735
NANDO:2201034	http://nanbyodata.jp/ontology/NANDO_2201034	遺伝性出血性末梢血管拡張症	Hereditary hemorrhagic telangiectasia	H00533	http://www.geneontology.org/formats/oboInOwl#hasDbXref	オスラー病	Hereditary hemorrhagic telangiectasia	https://identifiers.org/kegg.disease:H00533
NANDO:2201034	http://nanbyodata.jp/ontology/NANDO_2201034	遺伝性出血性末梢血管拡張症	Hereditary hemorrhagic telangiectasia	H00533	http://www.geneontology.org/formats/oboInOwl#hasDbXref	遺伝性出血性毛細血管拡張症	Hereditary hemorrhagic telangiectasia	https://identifiers.org/kegg.disease:H00533
NANDO:2201034	http://nanbyodata.jp/ontology/NANDO_2201034	遺伝性出血性末梢血管拡張症	Hereditary hemorrhagic telangiectasia	H00533	http://www.geneontology.org/formats/oboInOwl#hasDbXref	オスラー病	Osler disease	https://identifiers.org/kegg.disease:H00533
NANDO:2201034	http://nanbyodata.jp/ontology/NANDO_2201034	遺伝性出血性末梢血管拡張症	Hereditary hemorrhagic telangiectasia	H00533	http://www.geneontology.org/formats/oboInOwl#hasDbXref	遺伝性出血性毛細血管拡張症	Osler disease	https://identifiers.org/kegg.disease:H00533
NANDO:2201190	http://nanbyodata.jp/ontology/NANDO_2201190	β-マンノシドーシス	Beta-mannosidosis	H00140	http://www.geneontology.org/formats/oboInOwl#hasDbXref	β-マンノシドーシス	beta-Mannosidosis	https://identifiers.org/kegg.disease:H00140
NANDO:2201292	http://nanbyodata.jp/ontology/NANDO_2201292	アラン・ハーンドン・ダドリー症候群	Allan-Herndon-Dudley syndrome	H00650	http://www.geneontology.org/formats/oboInOwl#hasDbXref	Allan-Herndon-Dudley 症候群	Allan-Herndon-Dudley syndrome	https://identifiers.org/kegg.disease:H00650
NANDO:2201292	http://nanbyodata.jp/ontology/NANDO_2201292	アラン・ハーンドン・ダドリー症候群	Allan-Herndon-Dudley syndrome	H00650	http://www.geneontology.org/formats/oboInOwl#hasDbXref	Allan-Herndon-Dudley 症候群	Monocarboxylate transporter 8 deficiency	https://identifiers.org/kegg.disease:H00650
NANDO:2201322	http://nanbyodata.jp/ontology/NANDO_2201322	視神経脊髄炎	Neuromyelitis optica	H01491	http://www.geneontology.org/formats/oboInOwl#hasDbXref	視神経脊髄炎	Neuromyelitis optica	https://identifiers.org/kegg.disease:H01491
NANDO:2201322	http://nanbyodata.jp/ontology/NANDO_2201322	視神経脊髄炎	Neuromyelitis optica	H01491	http://www.geneontology.org/formats/oboInOwl#hasDbXref	デビック病	Neuromyelitis optica	https://identifiers.org/kegg.disease:H01491
NANDO:2201322	http://nanbyodata.jp/ontology/NANDO_2201322	視神経脊髄炎	Neuromyelitis optica	H01491	http://www.geneontology.org/formats/oboInOwl#hasDbXref	視神経脊髄炎	Devic disease	https://identifiers.org/kegg.disease:H01491
NANDO:2201322	http://nanbyodata.jp/ontology/NANDO_2201322	視神経脊髄炎	Neuromyelitis optica	H01491	http://www.geneontology.org/formats/oboInOwl#hasDbXref	デビック病	Devic disease	https://identifiers.org/kegg.disease:H01491
NANDO:2201341	http://nanbyodata.jp/ontology/NANDO_2201341	単純型表皮水疱症	Epidermolysis bullosa simplex	H00584	http://www.geneontology.org/formats/oboInOwl#hasDbXref	単純型表皮水疱症	Epidermolysis bullosa simplex	https://identifiers.org/kegg.disease:H00584
NANDO:2201342	http://nanbyodata.jp/ontology/NANDO_2201342	接合部型表皮水疱症	Junctional epidermolysis bullosa	H00586	http://www.geneontology.org/formats/oboInOwl#hasDbXref	接合部型表皮水疱症	Epidermolysis bullosa, junctional	https://identifiers.org/kegg.disease:H00586
NANDO:2201343	http://nanbyodata.jp/ontology/NANDO_2201343	栄養障害型表皮水疱症	Dystrophic epidermolysis bullosa	H00587	http://www.geneontology.org/formats/oboInOwl#hasDbXref	栄養障害型表皮水疱症	Epidermolysis bullosa, dystrophica	https://identifiers.org/kegg.disease:H00587
NANDO:2201348	http://nanbyodata.jp/ontology/NANDO_2201348	先天性脊椎骨端異形成症	Spondyloepiphyseal dysplasia congenita	H00519	http://www.geneontology.org/formats/oboInOwl#hasDbXref	先天性脊椎骨端異形成	Spondyloepiphyseal dysplasia congenita	https://identifiers.org/kegg.disease:H00519
NANDO:2201361	http://nanbyodata.jp/ontology/NANDO_2201361	Greenberg骨異形成症	Greenberg dysplasia	H00447	http://www.geneontology.org/formats/oboInOwl#hasDbXref	グリーンバーグ骨異形成症	Greenberg dysplasia	https://identifiers.org/kegg.disease:H00447
NANDO:2201361	http://nanbyodata.jp/ontology/NANDO_2201361	Greenberg骨異形成症	Greenberg dysplasia	H00447	http://www.geneontology.org/formats/oboInOwl#hasDbXref	グリーンバーグ骨異形成症	HEM skeletal dysplasia	https://identifiers.org/kegg.disease:H00447
NANDO:2201366	http://nanbyodata.jp/ontology/NANDO_2201366	頭蓋骨幹端異形成症	Craniometaphyseal dysplasia	H00491	http://www.geneontology.org/formats/oboInOwl#hasDbXref	頭蓋骨幹異形成症	Craniometaphyseal dysplasia	https://identifiers.org/kegg.disease:H00491
NANDO:2201367	http://nanbyodata.jp/ontology/NANDO_2201367	骨幹端異形成症	Metaphyseal dysplasias	H00479	http://www.geneontology.org/formats/oboInOwl#hasDbXref	骨幹端異形成症	Metaphyseal dysplasias	https://identifiers.org/kegg.disease:H00479
NANDO:2201368	http://nanbyodata.jp/ontology/NANDO_2201368	頭蓋骨幹異形成症	Craniodiaphyseal dysplasia	H00491	http://www.geneontology.org/formats/oboInOwl#hasDbXref	頭蓋骨幹異形成症	Craniometaphyseal dysplasia	https://identifiers.org/kegg.disease:H00491
NANDO:2201385	http://nanbyodata.jp/ontology/NANDO_2201385	ギャロウェイ・モワト症候群	Galloway-Mowat syndrome	H01722	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ギャロウェイ・モワト症候群	Galloway-Mowat syndrome	https://identifiers.org/kegg.disease:H01722
NANDO:2201392	http://nanbyodata.jp/ontology/NANDO_2201392	ホルト・オーラム症候群	Holt-Oram syndrome	H00433	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ホルト・オラム症候群	Holt-Oram syndrome	https://identifiers.org/kegg.disease:H00433
NANDO:2201394	http://nanbyodata.jp/ontology/NANDO_2201394	片側巨脳症	Hemimegaloencephaly	H01833	http://www.geneontology.org/formats/oboInOwl#hasDbXref	片側巨脳症	Hemimegalencephaly	https://identifiers.org/kegg.disease:H01833
NANDO:2201397	http://nanbyodata.jp/ontology/NANDO_2201397	アイカルディ症候群	Aicardi syndrome	H01776	http://www.geneontology.org/formats/oboInOwl#hasDbXref	アイカルディ症候群	Aicardi syndrome	https://identifiers.org/kegg.disease:H01776
NANDO:2201398	http://nanbyodata.jp/ontology/NANDO_2201398	大田原症候群	Ohtahara syndrome	H00606	http://www.geneontology.org/formats/oboInOwl#hasDbXref	大田原症候群	Ohtahara syndrome	https://identifiers.org/kegg.disease:H00606
NANDO:2201398	http://nanbyodata.jp/ontology/NANDO_2201398	大田原症候群	Ohtahara syndrome	H00606	http://www.geneontology.org/formats/oboInOwl#hasDbXref	早期乳児てんかん性脳症	Ohtahara syndrome	https://identifiers.org/kegg.disease:H00606
NANDO:2201398	http://nanbyodata.jp/ontology/NANDO_2201398	大田原症候群	Ohtahara syndrome	H00606	http://www.geneontology.org/formats/oboInOwl#hasDbXref	発達性およびてんかん性脳症	Ohtahara syndrome	https://identifiers.org/kegg.disease:H00606
NANDO:2201398	http://nanbyodata.jp/ontology/NANDO_2201398	大田原症候群	Ohtahara syndrome	H00606	http://www.geneontology.org/formats/oboInOwl#hasDbXref	大田原症候群	Developmental and epileptic encephalopathy	https://identifiers.org/kegg.disease:H00606
NANDO:2201398	http://nanbyodata.jp/ontology/NANDO_2201398	大田原症候群	Ohtahara syndrome	H00606	http://www.geneontology.org/formats/oboInOwl#hasDbXref	早期乳児てんかん性脳症	Developmental and epileptic encephalopathy	https://identifiers.org/kegg.disease:H00606
NANDO:2201398	http://nanbyodata.jp/ontology/NANDO_2201398	大田原症候群	Ohtahara syndrome	H00606	http://www.geneontology.org/formats/oboInOwl#hasDbXref	発達性およびてんかん性脳症	Developmental and epileptic encephalopathy	https://identifiers.org/kegg.disease:H00606
NANDO:2201398	http://nanbyodata.jp/ontology/NANDO_2201398	大田原症候群	Ohtahara syndrome	H00606	http://www.geneontology.org/formats/oboInOwl#hasDbXref	大田原症候群	Early infantile epileptic encephalopathy	https://identifiers.org/kegg.disease:H00606
NANDO:2201398	http://nanbyodata.jp/ontology/NANDO_2201398	大田原症候群	Ohtahara syndrome	H00606	http://www.geneontology.org/formats/oboInOwl#hasDbXref	早期乳児てんかん性脳症	Early infantile epileptic encephalopathy	https://identifiers.org/kegg.disease:H00606
NANDO:2201398	http://nanbyodata.jp/ontology/NANDO_2201398	大田原症候群	Ohtahara syndrome	H00606	http://www.geneontology.org/formats/oboInOwl#hasDbXref	発達性およびてんかん性脳症	Early infantile epileptic encephalopathy	https://identifiers.org/kegg.disease:H00606
NANDO:2201399	http://nanbyodata.jp/ontology/NANDO_2201399	環状20番染色体症候群	Ring chromosome 20 syndrome	H01831	http://www.geneontology.org/formats/oboInOwl#hasDbXref	環状２０番染色体症候群	Ring chromosome 20 syndrome	https://identifiers.org/kegg.disease:H01831
NANDO:2201403	http://nanbyodata.jp/ontology/NANDO_2201403	早期ミオクロニー脳症	Early myoclonic encephalopathy	H01819	http://www.geneontology.org/formats/oboInOwl#hasDbXref	早期ミオクロニー脳症	Early myoclonic encephalopathy	https://identifiers.org/kegg.disease:H01819
NANDO:2201406	http://nanbyodata.jp/ontology/NANDO_2201406	ミオクロニー欠神てんかん	Epilepsy with myoclonic absence	H01822	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ミオクロニー欠神てんかん	Epilepsy with myoclonic absence	https://identifiers.org/kegg.disease:H01822
NANDO:2201407	http://nanbyodata.jp/ontology/NANDO_2201407	ミオクロニー脱力発作を伴うてんかん	Epilepsy with myoclonic-atonic seizures	H01823	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ミオクロニー脱力発作を伴うてんかん	Doose syndrome	https://identifiers.org/kegg.disease:H01823
NANDO:2201407	http://nanbyodata.jp/ontology/NANDO_2201407	ミオクロニー脱力発作を伴うてんかん	Epilepsy with myoclonic-atonic seizures	H01823	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ドーゼ症候群	Doose syndrome	https://identifiers.org/kegg.disease:H01823
NANDO:2201407	http://nanbyodata.jp/ontology/NANDO_2201407	ミオクロニー脱力発作を伴うてんかん	Epilepsy with myoclonic-atonic seizures	H01823	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ミオクロニー脱力発作を伴うてんかん	Myoclonic-astatic epilepsy	https://identifiers.org/kegg.disease:H01823
NANDO:2201407	http://nanbyodata.jp/ontology/NANDO_2201407	ミオクロニー脱力発作を伴うてんかん	Epilepsy with myoclonic-atonic seizures	H01823	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ドーゼ症候群	Myoclonic-astatic epilepsy	https://identifiers.org/kegg.disease:H01823
NANDO:2201408	http://nanbyodata.jp/ontology/NANDO_2201408	遊走性焦点発作を伴う乳児てんかん	Epilepsy of infancy with migrating focal seizures	H01815	http://www.geneontology.org/formats/oboInOwl#hasDbXref	遊走性焦点発作を伴う乳児てんかん	Malignant migrating partial seizures in infancy	https://identifiers.org/kegg.disease:H01815
NANDO:2201410	http://nanbyodata.jp/ontology/NANDO_2201410	ピリドキシン依存性てんかん	Pyridoxine-dependent seizures	H01247	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ピリドキシン依存性てんかん	Pyridoxine-dependent epilepsy	https://identifiers.org/kegg.disease:H01247
NANDO:2201418	http://nanbyodata.jp/ontology/NANDO_2201418	コーエン症候群	Cohen syndrome	H00940	http://www.geneontology.org/formats/oboInOwl#hasDbXref	Cohen 症候群	Cohen syndrome	https://identifiers.org/kegg.disease:H00940
NANDO:2201419	http://nanbyodata.jp/ontology/NANDO_2201419	ピット・ホプキンス症候群	Pitt-Hopkins syndrome	H00756	http://www.geneontology.org/formats/oboInOwl#hasDbXref	Pitt-Hopkins 症候群	Pitt-Hopkins syndrome	https://identifiers.org/kegg.disease:H00756
NANDO:2201420	http://nanbyodata.jp/ontology/NANDO_2201420	限局性強皮症	Localized scleroderma/morphea	H01493	http://www.geneontology.org/formats/oboInOwl#hasDbXref	限局性強皮症	Localized Scleroderma	https://identifiers.org/kegg.disease:H01493
NANDO:2201420	http://nanbyodata.jp/ontology/NANDO_2201420	限局性強皮症	Localized scleroderma/morphea	H01493	http://www.geneontology.org/formats/oboInOwl#hasDbXref	モルフィア	Localized Scleroderma	https://identifiers.org/kegg.disease:H01493
NANDO:2201420	http://nanbyodata.jp/ontology/NANDO_2201420	限局性強皮症	Localized scleroderma/morphea	H01493	http://www.geneontology.org/formats/oboInOwl#hasDbXref	限局性強皮症	Morphea	https://identifiers.org/kegg.disease:H01493
NANDO:2201420	http://nanbyodata.jp/ontology/NANDO_2201420	限局性強皮症	Localized scleroderma/morphea	H01493	http://www.geneontology.org/formats/oboInOwl#hasDbXref	モルフィア	Morphea	https://identifiers.org/kegg.disease:H01493
NANDO:2201426	http://nanbyodata.jp/ontology/NANDO_2201426	タナトフォリック骨異形成症	Thanatophoric dysplasia	H01750	http://www.geneontology.org/formats/oboInOwl#hasDbXref	タナトフォリック骨異形成症	Thanatophoric dysplasia	https://identifiers.org/kegg.disease:H01750
NANDO:2201429	http://nanbyodata.jp/ontology/NANDO_2201429	ランドウ・クレフナー症候群	Landau-Kleffner syndrome	H01514	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ランドウ・クレフナー症候群	Landau-Kleffner syndrome	https://identifiers.org/kegg.disease:H01514
NANDO:2201434	http://nanbyodata.jp/ontology/NANDO_2201434	一過性新生児糖尿病	Transient neonatal diabetes mellitus	H00513	http://www.geneontology.org/formats/oboInOwl#hasDbXref	新生児一過性糖尿病	Transient neonatal diabetes mellitus	https://identifiers.org/kegg.disease:H00513
NANDO:2201435	http://nanbyodata.jp/ontology/NANDO_2201435	永続性新生児糖尿病	Permanent neonatal diabetes mellitus	H00512	http://www.geneontology.org/formats/oboInOwl#hasDbXref	新生児永続型糖尿病	Permanent neonatal diabetes mellitus	https://identifiers.org/kegg.disease:H00512
NANDO:2201439	http://nanbyodata.jp/ontology/NANDO_2201439	好酸球性食道炎	Eosinophilic esophagitis	H01361	http://www.geneontology.org/formats/oboInOwl#hasDbXref	好酸球性食道炎	Eosinophilic esophagitis	https://identifiers.org/kegg.disease:H01361
NANDO:2201445	http://nanbyodata.jp/ontology/NANDO_2201445	後天性全身性脂肪萎縮症	Acquired generalized lipodystrophy	H01474	http://www.geneontology.org/formats/oboInOwl#hasDbXref	後天性全身性脂肪萎縮症	Acquired generalized lipodystrophy	https://identifiers.org/kegg.disease:H01474
NANDO:2201445	http://nanbyodata.jp/ontology/NANDO_2201445	後天性全身性脂肪萎縮症	Acquired generalized lipodystrophy	H01474	http://www.geneontology.org/formats/oboInOwl#hasDbXref	Lawrence 症候群	Acquired generalized lipodystrophy	https://identifiers.org/kegg.disease:H01474
NANDO:2201445	http://nanbyodata.jp/ontology/NANDO_2201445	後天性全身性脂肪萎縮症	Acquired generalized lipodystrophy	H01474	http://www.geneontology.org/formats/oboInOwl#hasDbXref	後天性全身性脂肪萎縮症	Lawrence syndrome	https://identifiers.org/kegg.disease:H01474
NANDO:2201445	http://nanbyodata.jp/ontology/NANDO_2201445	後天性全身性脂肪萎縮症	Acquired generalized lipodystrophy	H01474	http://www.geneontology.org/formats/oboInOwl#hasDbXref	Lawrence 症候群	Lawrence syndrome	https://identifiers.org/kegg.disease:H01474
NANDO:2201470	http://nanbyodata.jp/ontology/NANDO_2201470	遺伝性鉄芽球性貧血	Hereditary sideroblastic anemia	H00982	http://www.geneontology.org/formats/oboInOwl#hasDbXref	遺伝性鉄芽球性貧血	Sideroblastic anemia	https://identifiers.org/kegg.disease:H00982
NANDO:2201473	http://nanbyodata.jp/ontology/NANDO_2201473	肝外門脈閉塞症	Extrahepatic portal vein obstruction	H01687	http://www.geneontology.org/formats/oboInOwl#hasDbXref	肝外門脈閉塞症	Extrahepatic portal vein obstruction	https://identifiers.org/kegg.disease:H01687
NANDO:2201473	http://nanbyodata.jp/ontology/NANDO_2201473	肝外門脈閉塞症	Extrahepatic portal vein obstruction	H01687	http://www.geneontology.org/formats/oboInOwl#hasDbXref	肝外門脈閉塞症	Extrahepatic portal venous obstruction	https://identifiers.org/kegg.disease:H01687
NANDO:2201474	http://nanbyodata.jp/ontology/NANDO_2201474	特発性門脈圧亢進症	Idiopathic portal hypertension	H01686	http://www.geneontology.org/formats/oboInOwl#hasDbXref	バンチ症候群	Banti syndrome	https://identifiers.org/kegg.disease:H01686
NANDO:2201474	http://nanbyodata.jp/ontology/NANDO_2201474	特発性門脈圧亢進症	Idiopathic portal hypertension	H01686	http://www.geneontology.org/formats/oboInOwl#hasDbXref	特発性門脈圧亢進症	Banti syndrome	https://identifiers.org/kegg.disease:H01686
NANDO:2201474	http://nanbyodata.jp/ontology/NANDO_2201474	特発性門脈圧亢進症	Idiopathic portal hypertension	H01686	http://www.geneontology.org/formats/oboInOwl#hasDbXref	非硬変症性門脈線維症	Banti syndrome	https://identifiers.org/kegg.disease:H01686
NANDO:2201474	http://nanbyodata.jp/ontology/NANDO_2201474	特発性門脈圧亢進症	Idiopathic portal hypertension	H01686	http://www.geneontology.org/formats/oboInOwl#hasDbXref	バンチ症候群	Idiopathic portal hypertension	https://identifiers.org/kegg.disease:H01686
NANDO:2201474	http://nanbyodata.jp/ontology/NANDO_2201474	特発性門脈圧亢進症	Idiopathic portal hypertension	H01686	http://www.geneontology.org/formats/oboInOwl#hasDbXref	特発性門脈圧亢進症	Idiopathic portal hypertension	https://identifiers.org/kegg.disease:H01686
NANDO:2201474	http://nanbyodata.jp/ontology/NANDO_2201474	特発性門脈圧亢進症	Idiopathic portal hypertension	H01686	http://www.geneontology.org/formats/oboInOwl#hasDbXref	非硬変症性門脈線維症	Idiopathic portal hypertension	https://identifiers.org/kegg.disease:H01686
NANDO:2201474	http://nanbyodata.jp/ontology/NANDO_2201474	特発性門脈圧亢進症	Idiopathic portal hypertension	H01686	http://www.geneontology.org/formats/oboInOwl#hasDbXref	バンチ症候群	Non-cirrhotic portal fibrosis	https://identifiers.org/kegg.disease:H01686
NANDO:2201474	http://nanbyodata.jp/ontology/NANDO_2201474	特発性門脈圧亢進症	Idiopathic portal hypertension	H01686	http://www.geneontology.org/formats/oboInOwl#hasDbXref	特発性門脈圧亢進症	Non-cirrhotic portal fibrosis	https://identifiers.org/kegg.disease:H01686
NANDO:2201474	http://nanbyodata.jp/ontology/NANDO_2201474	特発性門脈圧亢進症	Idiopathic portal hypertension	H01686	http://www.geneontology.org/formats/oboInOwl#hasDbXref	非硬変症性門脈線維症	Non-cirrhotic portal fibrosis	https://identifiers.org/kegg.disease:H01686
NANDO:2201475	http://nanbyodata.jp/ontology/NANDO_2201475	バッド・キアリ症候群	Budd-Chiari syndrome	H01433	http://www.geneontology.org/formats/oboInOwl#hasDbXref	バット・キアリ症候群	Budd-Chiari syndrome	https://identifiers.org/kegg.disease:H01433
NANDO:1201116	http://nanbyodata.jp/ontology/NANDO_1201116	ロウ症候群	Lowe syndrome	H00692	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ロウ症候群	Lowe syndrome	https://identifiers.org/kegg.disease:H00692
NANDO:1201116	http://nanbyodata.jp/ontology/NANDO_1201116	ロウ症候群	Lowe syndrome	H00692	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ロウ症候群	Oculocerebrorenal Dystrophy (OCRL)	https://identifiers.org/kegg.disease:H00692
NANDO:1201117	http://nanbyodata.jp/ontology/NANDO_1201117	Andersen-Tawil症候群	Andersen-Tawil syndrome	H00748	http://www.geneontology.org/formats/oboInOwl#hasDbXref	Andersen-Tawil 症候群	Andersen-Tawil syndrome	https://identifiers.org/kegg.disease:H00748
NANDO:2100305	http://nanbyodata.jp/ontology/NANDO_2100305	脊髄空洞症	Syringomyelia	H01675	http://www.geneontology.org/formats/oboInOwl#hasDbXref	脊髄空洞症	Syringomyelia	https://identifiers.org/kegg.disease:H01675
NANDO:2100306	http://nanbyodata.jp/ontology/NANDO_2100306	非ジストロフィー性ミオトニー症候群	Non-dystrophic myotonia	H01780	http://www.geneontology.org/formats/oboInOwl#hasDbXref	非ジストロフィー性ミオトニー症候群	Non-dystrophic myotonia	https://identifiers.org/kegg.disease:H01780
NANDO:2100307	http://nanbyodata.jp/ontology/NANDO_2100307	遺伝性周期性四肢麻痺	Hereditary hyperkalemic periodic paralysis	H00215	http://www.geneontology.org/formats/oboInOwl#hasDbXref	遺伝性周期性四肢麻痺	Periodic paralysis	https://identifiers.org/kegg.disease:H00215
NANDO:2100309	http://nanbyodata.jp/ontology/NANDO_2100309	特発性後天性全身性無汗症	Acquired Idiopathic Generalized Anhidrosis	H01848	http://www.geneontology.org/formats/oboInOwl#hasDbXref	特発性後天性全身性無汗症	Acquired idiopathic generalized anhidrosis	https://identifiers.org/kegg.disease:H01848
NANDO:2201488	http://nanbyodata.jp/ontology/NANDO_2201488	脊髄空洞症	Syringomyelia	H01675	http://www.geneontology.org/formats/oboInOwl#hasDbXref	脊髄空洞症	Syringomyelia	https://identifiers.org/kegg.disease:H01675
NANDO:2201508	http://nanbyodata.jp/ontology/NANDO_2201508	非ジストロフィー性ミオトニー症候群	Non-dystrophic myotonia	H01780	http://www.geneontology.org/formats/oboInOwl#hasDbXref	非ジストロフィー性ミオトニー症候群	Non-dystrophic myotonia	https://identifiers.org/kegg.disease:H01780
NANDO:2201509	http://nanbyodata.jp/ontology/NANDO_2201509	先天性ミオトニー	Myotonia congenita	H00705	http://www.geneontology.org/formats/oboInOwl#hasDbXref	先天性ミオトニー	Myotonia congenita	https://identifiers.org/kegg.disease:H00705
NANDO:2201512	http://nanbyodata.jp/ontology/NANDO_2201512	先天性パラミオトニー	Paramyotonia congenita	H00743	http://www.geneontology.org/formats/oboInOwl#hasDbXref	先天性パラミオトニー	Paramyotonia congenita	https://identifiers.org/kegg.disease:H00743
NANDO:2201513	http://nanbyodata.jp/ontology/NANDO_2201513	ナトリウムチャネルミオトニー	Sodium channel myotonia	H00744	http://www.geneontology.org/formats/oboInOwl#hasDbXref	カリウム惹起性ミオトニー	Sodium channel myotonia	https://identifiers.org/kegg.disease:H00744
NANDO:2201513	http://nanbyodata.jp/ontology/NANDO_2201513	ナトリウムチャネルミオトニー	Sodium channel myotonia	H00744	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ナトリウムチャネルミオトニー	Sodium channel myotonia	https://identifiers.org/kegg.disease:H00744
NANDO:2201513	http://nanbyodata.jp/ontology/NANDO_2201513	ナトリウムチャネルミオトニー	Sodium channel myotonia	H00744	http://www.geneontology.org/formats/oboInOwl#hasDbXref	カリウム惹起性ミオトニー	Potassium-aggravated myotonia	https://identifiers.org/kegg.disease:H00744
NANDO:2201513	http://nanbyodata.jp/ontology/NANDO_2201513	ナトリウムチャネルミオトニー	Sodium channel myotonia	H00744	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ナトリウムチャネルミオトニー	Potassium-aggravated myotonia	https://identifiers.org/kegg.disease:H00744
NANDO:2201516	http://nanbyodata.jp/ontology/NANDO_2201516	Andersen-Tawil症候群	Andersen-Tawil syndrome	H00748	http://www.geneontology.org/formats/oboInOwl#hasDbXref	Andersen-Tawil 症候群	Andersen-Tawil syndrome	https://identifiers.org/kegg.disease:H00748
NANDO:2201523	http://nanbyodata.jp/ontology/NANDO_2201523	鏡・緒方症候群	Kagami-Ogata syndrome	H01801	http://www.geneontology.org/formats/oboInOwl#hasDbXref	鏡・緒方症候群	Kagami-Ogata syndrome	https://identifiers.org/kegg.disease:H01801
NANDO:2201523	http://nanbyodata.jp/ontology/NANDO_2201523	鏡・緒方症候群	Kagami-Ogata syndrome	H01801	http://www.geneontology.org/formats/oboInOwl#hasDbXref	第１４番染色体父親性ダイソミー症候群	Kagami-Ogata syndrome	https://identifiers.org/kegg.disease:H01801
NANDO:2201523	http://nanbyodata.jp/ontology/NANDO_2201523	鏡・緒方症候群	Kagami-Ogata syndrome	H01801	http://www.geneontology.org/formats/oboInOwl#hasDbXref	鏡・緒方症候群	Paternal uniparental disomy 14	https://identifiers.org/kegg.disease:H01801
NANDO:2201523	http://nanbyodata.jp/ontology/NANDO_2201523	鏡・緒方症候群	Kagami-Ogata syndrome	H01801	http://www.geneontology.org/formats/oboInOwl#hasDbXref	第１４番染色体父親性ダイソミー症候群	Paternal uniparental disomy 14	https://identifiers.org/kegg.disease:H01801
NANDO:2201526	http://nanbyodata.jp/ontology/NANDO_2201526	トリーチャーコリンズ症候群	Treacher Collins syndrome	H00610	http://www.geneontology.org/formats/oboInOwl#hasDbXref	トレチャーコリンズ症候群	Treacher Collins syndrome	https://identifiers.org/kegg.disease:H00610
NANDO:2201527	http://nanbyodata.jp/ontology/NANDO_2201527	ロスムンド・トムソン症候群	Rothmund-Thomson syndrome	H01734	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ロスムンド・トムソン症候群	Rothmund-Thomson syndrome	https://identifiers.org/kegg.disease:H01734
NANDO:2201532	http://nanbyodata.jp/ontology/NANDO_2201532	特発性後天性全身性無汗症	Acquired Idiopathic Generalized Anhidrosis	H01848	http://www.geneontology.org/formats/oboInOwl#hasDbXref	特発性後天性全身性無汗症	Acquired idiopathic generalized anhidrosis	https://identifiers.org/kegg.disease:H01848
NANDO:1201158	http://nanbyodata.jp/ontology/NANDO_1201158	マルファン症候群	Marfan syndrome	H00653	http://www.geneontology.org/formats/oboInOwl#hasDbXref	マルファン症候群	Marfan syndrome	https://identifiers.org/kegg.disease:H00653
NANDO:2200509	http://nanbyodata.jp/ontology/NANDO_2200509	カルニチンパルミトイルトランスフェラーゼI欠損症	Carnitine palmitoyltransferase I deficiency	H01981	http://www.geneontology.org/formats/oboInOwl#hasDbXref	カルニチンパルミトイルトランスフェラーゼ I 欠損症	Carnitine palmitoyltransferase I deficiency	https://identifiers.org/kegg.disease:H01981
NANDO:2200510	http://nanbyodata.jp/ontology/NANDO_2200510	カルニチンパルミトイルトランスフェラーゼII欠損症	Carnitine palmitoyltransferase II deficiency	H01982	http://www.geneontology.org/formats/oboInOwl#hasDbXref	カルニチンパルミトイルトランスフェラーゼ II 欠損症	Carnitine palmitoyltransferase II deficiency	https://identifiers.org/kegg.disease:H01982
NANDO:2200511	http://nanbyodata.jp/ontology/NANDO_2200511	カルニチン/アシルカルニチントランスロカーゼ欠損症	Carnitine-acylcarnitine translocase deficiency	H01983	http://www.geneontology.org/formats/oboInOwl#hasDbXref	カルニチン-アシルカルニチントランスロカーゼ欠損症	Carnitine-acylcarnitine translocase deficiency	https://identifiers.org/kegg.disease:H01983
NANDO:2200514	http://nanbyodata.jp/ontology/NANDO_2200514	短鎖アシルCoA脱水素酵素欠損症	Short-chain acyl-CoA dehydrogenase deficiency	H01980	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ACADS 欠損症	SCAD deficiency	https://identifiers.org/kegg.disease:H01980
NANDO:2200514	http://nanbyodata.jp/ontology/NANDO_2200514	短鎖アシルCoA脱水素酵素欠損症	Short-chain acyl-CoA dehydrogenase deficiency	H01980	http://www.geneontology.org/formats/oboInOwl#hasDbXref	SCAD 欠損症	SCAD deficiency	https://identifiers.org/kegg.disease:H01980
NANDO:2200514	http://nanbyodata.jp/ontology/NANDO_2200514	短鎖アシルCoA脱水素酵素欠損症	Short-chain acyl-CoA dehydrogenase deficiency	H01980	http://www.geneontology.org/formats/oboInOwl#hasDbXref	短鎖アシルCoA デヒドロゲナーゼ欠損症	SCAD deficiency	https://identifiers.org/kegg.disease:H01980
NANDO:2200514	http://nanbyodata.jp/ontology/NANDO_2200514	短鎖アシルCoA脱水素酵素欠損症	Short-chain acyl-CoA dehydrogenase deficiency	H01980	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ACADS 欠損症	Short-chain acyl-CoA dehydrogenase deficiency	https://identifiers.org/kegg.disease:H01980
NANDO:2200514	http://nanbyodata.jp/ontology/NANDO_2200514	短鎖アシルCoA脱水素酵素欠損症	Short-chain acyl-CoA dehydrogenase deficiency	H01980	http://www.geneontology.org/formats/oboInOwl#hasDbXref	SCAD 欠損症	Short-chain acyl-CoA dehydrogenase deficiency	https://identifiers.org/kegg.disease:H01980
NANDO:2200514	http://nanbyodata.jp/ontology/NANDO_2200514	短鎖アシルCoA脱水素酵素欠損症	Short-chain acyl-CoA dehydrogenase deficiency	H01980	http://www.geneontology.org/formats/oboInOwl#hasDbXref	短鎖アシルCoA デヒドロゲナーゼ欠損症	Short-chain acyl-CoA dehydrogenase deficiency	https://identifiers.org/kegg.disease:H01980
NANDO:2200514	http://nanbyodata.jp/ontology/NANDO_2200514	短鎖アシルCoA脱水素酵素欠損症	Short-chain acyl-CoA dehydrogenase deficiency	H01980	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ACADS 欠損症	ACADS deficiency	https://identifiers.org/kegg.disease:H01980
NANDO:2200514	http://nanbyodata.jp/ontology/NANDO_2200514	短鎖アシルCoA脱水素酵素欠損症	Short-chain acyl-CoA dehydrogenase deficiency	H01980	http://www.geneontology.org/formats/oboInOwl#hasDbXref	SCAD 欠損症	ACADS deficiency	https://identifiers.org/kegg.disease:H01980
NANDO:2200514	http://nanbyodata.jp/ontology/NANDO_2200514	短鎖アシルCoA脱水素酵素欠損症	Short-chain acyl-CoA dehydrogenase deficiency	H01980	http://www.geneontology.org/formats/oboInOwl#hasDbXref	短鎖アシルCoA デヒドロゲナーゼ欠損症	ACADS deficiency	https://identifiers.org/kegg.disease:H01980
NANDO:2200520	http://nanbyodata.jp/ontology/NANDO_2200520	フマラーゼ欠損症	Fumarase deficiency	H02004	http://www.geneontology.org/formats/oboInOwl#hasDbXref	フマラーゼ欠損症	Fumarase deficiency	https://identifiers.org/kegg.disease:H02004
NANDO:2200520	http://nanbyodata.jp/ontology/NANDO_2200520	フマラーゼ欠損症	Fumarase deficiency	H02004	http://www.geneontology.org/formats/oboInOwl#hasDbXref	フマル酸尿症	Fumarase deficiency	https://identifiers.org/kegg.disease:H02004
NANDO:2200520	http://nanbyodata.jp/ontology/NANDO_2200520	フマラーゼ欠損症	Fumarase deficiency	H02004	http://www.geneontology.org/formats/oboInOwl#hasDbXref	フマラーゼ欠損症	Fumaric aciduria	https://identifiers.org/kegg.disease:H02004
NANDO:2200520	http://nanbyodata.jp/ontology/NANDO_2200520	フマラーゼ欠損症	Fumarase deficiency	H02004	http://www.geneontology.org/formats/oboInOwl#hasDbXref	フマル酸尿症	Fumaric aciduria	https://identifiers.org/kegg.disease:H02004
NANDO:2200532	http://nanbyodata.jp/ontology/NANDO_2200532	ガラクトース-1-リン酸ウリジルトランスフェラーゼ欠損症	Galactose-1-phosphate uridyltransferase deficiency	H02008	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ガラクトース-1-リン酸ウリジルトランスフェラーゼ欠損症	Classic galactosemia	https://identifiers.org/kegg.disease:H02008
NANDO:2200532	http://nanbyodata.jp/ontology/NANDO_2200532	ガラクトース-1-リン酸ウリジルトランスフェラーゼ欠損症	Galactose-1-phosphate uridyltransferase deficiency	H02008	http://www.geneontology.org/formats/oboInOwl#hasDbXref	古典型ガラクトース血症	Classic galactosemia	https://identifiers.org/kegg.disease:H02008
NANDO:2200532	http://nanbyodata.jp/ontology/NANDO_2200532	ガラクトース-1-リン酸ウリジルトランスフェラーゼ欠損症	Galactose-1-phosphate uridyltransferase deficiency	H02008	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ガラクトース血症 I 型	Classic galactosemia	https://identifiers.org/kegg.disease:H02008
NANDO:2200532	http://nanbyodata.jp/ontology/NANDO_2200532	ガラクトース-1-リン酸ウリジルトランスフェラーゼ欠損症	Galactose-1-phosphate uridyltransferase deficiency	H02008	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ガラクトース-1-リン酸ウリジルトランスフェラーゼ欠損症	Galactose-1P uridylyltransferase deficiency	https://identifiers.org/kegg.disease:H02008
NANDO:2200532	http://nanbyodata.jp/ontology/NANDO_2200532	ガラクトース-1-リン酸ウリジルトランスフェラーゼ欠損症	Galactose-1-phosphate uridyltransferase deficiency	H02008	http://www.geneontology.org/formats/oboInOwl#hasDbXref	古典型ガラクトース血症	Galactose-1P uridylyltransferase deficiency	https://identifiers.org/kegg.disease:H02008
NANDO:2200532	http://nanbyodata.jp/ontology/NANDO_2200532	ガラクトース-1-リン酸ウリジルトランスフェラーゼ欠損症	Galactose-1-phosphate uridyltransferase deficiency	H02008	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ガラクトース血症 I 型	Galactose-1P uridylyltransferase deficiency	https://identifiers.org/kegg.disease:H02008
NANDO:2200532	http://nanbyodata.jp/ontology/NANDO_2200532	ガラクトース-1-リン酸ウリジルトランスフェラーゼ欠損症	Galactose-1-phosphate uridyltransferase deficiency	H02008	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ガラクトース-1-リン酸ウリジルトランスフェラーゼ欠損症	Galactosemia type I	https://identifiers.org/kegg.disease:H02008
NANDO:2200532	http://nanbyodata.jp/ontology/NANDO_2200532	ガラクトース-1-リン酸ウリジルトランスフェラーゼ欠損症	Galactose-1-phosphate uridyltransferase deficiency	H02008	http://www.geneontology.org/formats/oboInOwl#hasDbXref	古典型ガラクトース血症	Galactosemia type I	https://identifiers.org/kegg.disease:H02008
NANDO:2200532	http://nanbyodata.jp/ontology/NANDO_2200532	ガラクトース-1-リン酸ウリジルトランスフェラーゼ欠損症	Galactose-1-phosphate uridyltransferase deficiency	H02008	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ガラクトース血症 I 型	Galactosemia type I	https://identifiers.org/kegg.disease:H02008
NANDO:2200533	http://nanbyodata.jp/ontology/NANDO_2200533	ガラクトキナーゼ欠損症	Galactokinase deficiency	H02009	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ガラクトキナーゼ欠損症	Galactokinase deficiency	https://identifiers.org/kegg.disease:H02009
NANDO:2200533	http://nanbyodata.jp/ontology/NANDO_2200533	ガラクトキナーゼ欠損症	Galactokinase deficiency	H02009	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ガラクトース血症 II 型	Galactokinase deficiency	https://identifiers.org/kegg.disease:H02009
NANDO:2200533	http://nanbyodata.jp/ontology/NANDO_2200533	ガラクトキナーゼ欠損症	Galactokinase deficiency	H02009	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ガラクトキナーゼ欠損症	Galactosemia II	https://identifiers.org/kegg.disease:H02009
NANDO:2200533	http://nanbyodata.jp/ontology/NANDO_2200533	ガラクトキナーゼ欠損症	Galactokinase deficiency	H02009	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ガラクトース血症 II 型	Galactosemia II	https://identifiers.org/kegg.disease:H02009
NANDO:2200536	http://nanbyodata.jp/ontology/NANDO_2200536	ホスホエノールピルビン酸カルボキシキナーゼ欠損症	Phosphoenolpyruvate carboxykinase deficiency	H02520	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ホスホエノールピルビン酸カルボキシキナーゼ欠損症	Phosphoenolpyruvate carboxykinase deficiency	https://identifiers.org/kegg.disease:H02520
NANDO:2200538	http://nanbyodata.jp/ontology/NANDO_2200538	糖原病I型	Glycogen storage disease type I	H01939	http://www.geneontology.org/formats/oboInOwl#hasDbXref	フォン・ギールケ病	Glycogen storage disease type I	https://identifiers.org/kegg.disease:H01939
NANDO:2200538	http://nanbyodata.jp/ontology/NANDO_2200538	糖原病I型	Glycogen storage disease type I	H01939	http://www.geneontology.org/formats/oboInOwl#hasDbXref	糖原病 I 型	Glycogen storage disease type I	https://identifiers.org/kegg.disease:H01939
NANDO:2200538	http://nanbyodata.jp/ontology/NANDO_2200538	糖原病I型	Glycogen storage disease type I	H01939	http://www.geneontology.org/formats/oboInOwl#hasDbXref	フォン・ギールケ病	Von Gierke disease	https://identifiers.org/kegg.disease:H01939
NANDO:2200538	http://nanbyodata.jp/ontology/NANDO_2200538	糖原病I型	Glycogen storage disease type I	H01939	http://www.geneontology.org/formats/oboInOwl#hasDbXref	糖原病 I 型	Von Gierke disease	https://identifiers.org/kegg.disease:H01939
NANDO:2200539	http://nanbyodata.jp/ontology/NANDO_2200539	糖原病III型	Glycogen storage disease type III	H01941	http://www.geneontology.org/formats/oboInOwl#hasDbXref	コーリ病	Cori disease	https://identifiers.org/kegg.disease:H01941
NANDO:2200539	http://nanbyodata.jp/ontology/NANDO_2200539	糖原病III型	Glycogen storage disease type III	H01941	http://www.geneontology.org/formats/oboInOwl#hasDbXref	フォーブズ病	Cori disease	https://identifiers.org/kegg.disease:H01941
NANDO:2200539	http://nanbyodata.jp/ontology/NANDO_2200539	糖原病III型	Glycogen storage disease type III	H01941	http://www.geneontology.org/formats/oboInOwl#hasDbXref	糖原病 III 型	Cori disease	https://identifiers.org/kegg.disease:H01941
NANDO:2200539	http://nanbyodata.jp/ontology/NANDO_2200539	糖原病III型	Glycogen storage disease type III	H01941	http://www.geneontology.org/formats/oboInOwl#hasDbXref	コーリ病	Glycogen storage disease type III	https://identifiers.org/kegg.disease:H01941
NANDO:2200539	http://nanbyodata.jp/ontology/NANDO_2200539	糖原病III型	Glycogen storage disease type III	H01941	http://www.geneontology.org/formats/oboInOwl#hasDbXref	フォーブズ病	Glycogen storage disease type III	https://identifiers.org/kegg.disease:H01941
NANDO:2200539	http://nanbyodata.jp/ontology/NANDO_2200539	糖原病III型	Glycogen storage disease type III	H01941	http://www.geneontology.org/formats/oboInOwl#hasDbXref	糖原病 III 型	Glycogen storage disease type III	https://identifiers.org/kegg.disease:H01941
NANDO:2200539	http://nanbyodata.jp/ontology/NANDO_2200539	糖原病III型	Glycogen storage disease type III	H01941	http://www.geneontology.org/formats/oboInOwl#hasDbXref	コーリ病	Forbes disease	https://identifiers.org/kegg.disease:H01941
NANDO:2200539	http://nanbyodata.jp/ontology/NANDO_2200539	糖原病III型	Glycogen storage disease type III	H01941	http://www.geneontology.org/formats/oboInOwl#hasDbXref	フォーブズ病	Forbes disease	https://identifiers.org/kegg.disease:H01941
NANDO:2200539	http://nanbyodata.jp/ontology/NANDO_2200539	糖原病III型	Glycogen storage disease type III	H01941	http://www.geneontology.org/formats/oboInOwl#hasDbXref	糖原病 III 型	Forbes disease	https://identifiers.org/kegg.disease:H01941
NANDO:2200540	http://nanbyodata.jp/ontology/NANDO_2200540	糖原病IV型	Glycogen storage disease type IV	H01942	http://www.geneontology.org/formats/oboInOwl#hasDbXref	アンダーセン病	Andersen disease	https://identifiers.org/kegg.disease:H01942
NANDO:2200540	http://nanbyodata.jp/ontology/NANDO_2200540	糖原病IV型	Glycogen storage disease type IV	H01942	http://www.geneontology.org/formats/oboInOwl#hasDbXref	糖原病 IV 型	Andersen disease	https://identifiers.org/kegg.disease:H01942
NANDO:2200540	http://nanbyodata.jp/ontology/NANDO_2200540	糖原病IV型	Glycogen storage disease type IV	H01942	http://www.geneontology.org/formats/oboInOwl#hasDbXref	アンダーセン病	Glycogen storage disease type IV	https://identifiers.org/kegg.disease:H01942
NANDO:2200540	http://nanbyodata.jp/ontology/NANDO_2200540	糖原病IV型	Glycogen storage disease type IV	H01942	http://www.geneontology.org/formats/oboInOwl#hasDbXref	糖原病 IV 型	Glycogen storage disease type IV	https://identifiers.org/kegg.disease:H01942
NANDO:2200541	http://nanbyodata.jp/ontology/NANDO_2200541	糖原病V型	Glycogen storage disease type V	H01943	http://www.geneontology.org/formats/oboInOwl#hasDbXref	マッカードル病	Glycogen storage disease type V	https://identifiers.org/kegg.disease:H01943
NANDO:2200541	http://nanbyodata.jp/ontology/NANDO_2200541	糖原病V型	Glycogen storage disease type V	H01943	http://www.geneontology.org/formats/oboInOwl#hasDbXref	糖原病 V 型	Glycogen storage disease type V	https://identifiers.org/kegg.disease:H01943
NANDO:2200541	http://nanbyodata.jp/ontology/NANDO_2200541	糖原病V型	Glycogen storage disease type V	H01943	http://www.geneontology.org/formats/oboInOwl#hasDbXref	マッカードル病	McArdle disease	https://identifiers.org/kegg.disease:H01943
NANDO:2200541	http://nanbyodata.jp/ontology/NANDO_2200541	糖原病V型	Glycogen storage disease type V	H01943	http://www.geneontology.org/formats/oboInOwl#hasDbXref	糖原病 V 型	McArdle disease	https://identifiers.org/kegg.disease:H01943
NANDO:2200542	http://nanbyodata.jp/ontology/NANDO_2200542	糖原病VI型	Glycogen storage disease type VI	H01944	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ハース病	Glycogen storage disease type VI	https://identifiers.org/kegg.disease:H01944
NANDO:2200542	http://nanbyodata.jp/ontology/NANDO_2200542	糖原病VI型	Glycogen storage disease type VI	H01944	http://www.geneontology.org/formats/oboInOwl#hasDbXref	糖原病 VI 型	Glycogen storage disease type VI	https://identifiers.org/kegg.disease:H01944
NANDO:2200542	http://nanbyodata.jp/ontology/NANDO_2200542	糖原病VI型	Glycogen storage disease type VI	H01944	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ハース病	Hers disease	https://identifiers.org/kegg.disease:H01944
NANDO:2200542	http://nanbyodata.jp/ontology/NANDO_2200542	糖原病VI型	Glycogen storage disease type VI	H01944	http://www.geneontology.org/formats/oboInOwl#hasDbXref	糖原病 VI 型	Hers disease	https://identifiers.org/kegg.disease:H01944
NANDO:2200543	http://nanbyodata.jp/ontology/NANDO_2200543	糖原病VII型	Glycogen storage disease type VII	H01945	http://www.geneontology.org/formats/oboInOwl#hasDbXref	垂井病	Glycogen storage disease type VII	https://identifiers.org/kegg.disease:H01945
NANDO:2200543	http://nanbyodata.jp/ontology/NANDO_2200543	糖原病VII型	Glycogen storage disease type VII	H01945	http://www.geneontology.org/formats/oboInOwl#hasDbXref	糖原病 VII 型	Glycogen storage disease type VII	https://identifiers.org/kegg.disease:H01945
NANDO:2200543	http://nanbyodata.jp/ontology/NANDO_2200543	糖原病VII型	Glycogen storage disease type VII	H01945	http://www.geneontology.org/formats/oboInOwl#hasDbXref	垂井病	Tarui disease	https://identifiers.org/kegg.disease:H01945
NANDO:2200543	http://nanbyodata.jp/ontology/NANDO_2200543	糖原病VII型	Glycogen storage disease type VII	H01945	http://www.geneontology.org/formats/oboInOwl#hasDbXref	糖原病 VII 型	Tarui disease	https://identifiers.org/kegg.disease:H01945
NANDO:2200544	http://nanbyodata.jp/ontology/NANDO_2200544	糖原病IX型	Glycogen storage disease type IX	H01948	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ホスホリラーゼキナーゼ欠損症	Glycogen storage disease type IX	https://identifiers.org/kegg.disease:H01948
NANDO:2200544	http://nanbyodata.jp/ontology/NANDO_2200544	糖原病IX型	Glycogen storage disease type IX	H01948	http://www.geneontology.org/formats/oboInOwl#hasDbXref	糖原病 IX 型	Glycogen storage disease type IX	https://identifiers.org/kegg.disease:H01948
NANDO:2200544	http://nanbyodata.jp/ontology/NANDO_2200544	糖原病IX型	Glycogen storage disease type IX	H01948	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ホスホリラーゼキナーゼ欠損症	Phosphorylase kinase deficiency	https://identifiers.org/kegg.disease:H01948
NANDO:2200544	http://nanbyodata.jp/ontology/NANDO_2200544	糖原病IX型	Glycogen storage disease type IX	H01948	http://www.geneontology.org/formats/oboInOwl#hasDbXref	糖原病 IX 型	Phosphorylase kinase deficiency	https://identifiers.org/kegg.disease:H01948
NANDO:2200568	http://nanbyodata.jp/ontology/NANDO_2200568	ムコリピドーシスIII型	Mucolipidosis III	H02130	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ムコリピドーシス III 型	Mucolipidosis III	https://identifiers.org/kegg.disease:H02130
NANDO:2200568	http://nanbyodata.jp/ontology/NANDO_2200568	ムコリピドーシスIII型	Mucolipidosis III	H02130	http://www.geneontology.org/formats/oboInOwl#hasDbXref	偽 Hurler ポリジストロフィー	Mucolipidosis III	https://identifiers.org/kegg.disease:H02130
NANDO:2200568	http://nanbyodata.jp/ontology/NANDO_2200568	ムコリピドーシスIII型	Mucolipidosis III	H02130	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ムコリピドーシス III 型	Pseudo-Hurler polydystrophy	https://identifiers.org/kegg.disease:H02130
NANDO:2200568	http://nanbyodata.jp/ontology/NANDO_2200568	ムコリピドーシスIII型	Mucolipidosis III	H02130	http://www.geneontology.org/formats/oboInOwl#hasDbXref	偽 Hurler ポリジストロフィー	Pseudo-Hurler polydystrophy	https://identifiers.org/kegg.disease:H02130
NANDO:2200569	http://nanbyodata.jp/ontology/NANDO_2200569	ポンペ病	Pompe disease	H01940	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ポンペ病	Pompe disease	https://identifiers.org/kegg.disease:H01940
NANDO:2200569	http://nanbyodata.jp/ontology/NANDO_2200569	ポンペ病	Pompe disease	H01940	http://www.geneontology.org/formats/oboInOwl#hasDbXref	糖原病 II型	Pompe disease	https://identifiers.org/kegg.disease:H01940
NANDO:2200569	http://nanbyodata.jp/ontology/NANDO_2200569	ポンペ病	Pompe disease	H01940	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ポンペ病	Glycogen storage disease type II	https://identifiers.org/kegg.disease:H01940
NANDO:2200569	http://nanbyodata.jp/ontology/NANDO_2200569	ポンペ病	Pompe disease	H01940	http://www.geneontology.org/formats/oboInOwl#hasDbXref	糖原病 II型	Glycogen storage disease type II	https://identifiers.org/kegg.disease:H01940
NANDO:2200581	http://nanbyodata.jp/ontology/NANDO_2200581	オクシピタル・ホーン症候群	Occipital horn syndrome	H01859	http://www.geneontology.org/formats/oboInOwl#hasDbXref	オクシピタル・ホーン症候群	Occipital horn syndrome	https://identifiers.org/kegg.disease:H01859
NANDO:2200582	http://nanbyodata.jp/ontology/NANDO_2200582	無セルロプラスミン血症	Aceruloplasminemia	H02206	http://www.geneontology.org/formats/oboInOwl#hasDbXref	無セルロプラスミン血症	Aceruloplasminemia	https://identifiers.org/kegg.disease:H02206
NANDO:2200582	http://nanbyodata.jp/ontology/NANDO_2200582	無セルロプラスミン血症	Aceruloplasminemia	H02206	http://www.geneontology.org/formats/oboInOwl#hasDbXref	セルロプラスミン欠損症	Aceruloplasminemia	https://identifiers.org/kegg.disease:H02206
NANDO:2200582	http://nanbyodata.jp/ontology/NANDO_2200582	無セルロプラスミン血症	Aceruloplasminemia	H02206	http://www.geneontology.org/formats/oboInOwl#hasDbXref	無セルロプラスミン血症	Ceruloplasmin deficiency	https://identifiers.org/kegg.disease:H02206
NANDO:2200582	http://nanbyodata.jp/ontology/NANDO_2200582	無セルロプラスミン血症	Aceruloplasminemia	H02206	http://www.geneontology.org/formats/oboInOwl#hasDbXref	セルロプラスミン欠損症	Ceruloplasmin deficiency	https://identifiers.org/kegg.disease:H02206
NANDO:2200654	http://nanbyodata.jp/ontology/NANDO_2200654	メイ・ヘグリン異常症	May-Hegglin anomaly	H02051	http://www.geneontology.org/formats/oboInOwl#hasDbXref	メイ・ヘグリン異常	May-Hegglin anomaly	https://identifiers.org/kegg.disease:H02051
NANDO:2200668	http://nanbyodata.jp/ontology/NANDO_2200668	血小板型フォンウィルブランド病	Platelet-type von Willebrand disease	H02093	http://www.geneontology.org/formats/oboInOwl#hasDbXref	血小板型フォン・ヴィレブランド病	Platelet-type von Willebrand disease	https://identifiers.org/kegg.disease:H02093
NANDO:2200668	http://nanbyodata.jp/ontology/NANDO_2200668	血小板型フォンウィルブランド病	Platelet-type von Willebrand disease	H02093	http://www.geneontology.org/formats/oboInOwl#hasDbXref	血小板型フォン・ヴィレブランド病	Pseudo-von Willebrand disease	https://identifiers.org/kegg.disease:H02093
NANDO:2200682	http://nanbyodata.jp/ontology/NANDO_2200682	フォンウィルブランド病	Von Willebrand disease	H02092	http://www.geneontology.org/formats/oboInOwl#hasDbXref	フォン・ヴィレブランド病	von Willebrand disease	https://identifiers.org/kegg.disease:H02092
NANDO:2200696	http://nanbyodata.jp/ontology/NANDO_2200696	アデノシンデアミナーゼ欠損症	Adenosine deaminase deficiency	H02309	http://www.geneontology.org/formats/oboInOwl#hasDbXref	アデノシンデアミナーゼ欠損症	Adenosine deaminase deficiency	https://identifiers.org/kegg.disease:H02309
NANDO:2200697	http://nanbyodata.jp/ontology/NANDO_2200697	オーメン症候群	Omenn syndrome	H02554	http://www.geneontology.org/formats/oboInOwl#hasDbXref	Omenn 症候群	Omenn syndrome	https://identifiers.org/kegg.disease:H02554
NANDO:2200713	http://nanbyodata.jp/ontology/NANDO_2200713	高IgE症候群	Hyper-IgE syndrome	H01968	http://www.geneontology.org/formats/oboInOwl#hasDbXref	Buckley 症候群	Hyper-IgE syndrome	https://identifiers.org/kegg.disease:H01968
NANDO:2200713	http://nanbyodata.jp/ontology/NANDO_2200713	高IgE症候群	Hyper-IgE syndrome	H01968	http://www.geneontology.org/formats/oboInOwl#hasDbXref	Job 症候群	Hyper-IgE syndrome	https://identifiers.org/kegg.disease:H01968
NANDO:2200713	http://nanbyodata.jp/ontology/NANDO_2200713	高IgE症候群	Hyper-IgE syndrome	H01968	http://www.geneontology.org/formats/oboInOwl#hasDbXref	高 IgE 症候群	Hyper-IgE syndrome	https://identifiers.org/kegg.disease:H01968
NANDO:2200713	http://nanbyodata.jp/ontology/NANDO_2200713	高IgE症候群	Hyper-IgE syndrome	H01968	http://www.geneontology.org/formats/oboInOwl#hasDbXref	Buckley 症候群	Buckley syndrome	https://identifiers.org/kegg.disease:H01968
NANDO:2200713	http://nanbyodata.jp/ontology/NANDO_2200713	高IgE症候群	Hyper-IgE syndrome	H01968	http://www.geneontology.org/formats/oboInOwl#hasDbXref	Job 症候群	Buckley syndrome	https://identifiers.org/kegg.disease:H01968
NANDO:2200713	http://nanbyodata.jp/ontology/NANDO_2200713	高IgE症候群	Hyper-IgE syndrome	H01968	http://www.geneontology.org/formats/oboInOwl#hasDbXref	高 IgE 症候群	Buckley syndrome	https://identifiers.org/kegg.disease:H01968
NANDO:2200713	http://nanbyodata.jp/ontology/NANDO_2200713	高IgE症候群	Hyper-IgE syndrome	H01968	http://www.geneontology.org/formats/oboInOwl#hasDbXref	Buckley 症候群	Job syndrome	https://identifiers.org/kegg.disease:H01968
NANDO:2200713	http://nanbyodata.jp/ontology/NANDO_2200713	高IgE症候群	Hyper-IgE syndrome	H01968	http://www.geneontology.org/formats/oboInOwl#hasDbXref	Job 症候群	Job syndrome	https://identifiers.org/kegg.disease:H01968
NANDO:2200713	http://nanbyodata.jp/ontology/NANDO_2200713	高IgE症候群	Hyper-IgE syndrome	H01968	http://www.geneontology.org/formats/oboInOwl#hasDbXref	高 IgE 症候群	Job syndrome	https://identifiers.org/kegg.disease:H01968
NANDO:2200724	http://nanbyodata.jp/ontology/NANDO_2200724	チェディアック・東症候群	Chédiak-Higashi syndrome	H02021	http://www.geneontology.org/formats/oboInOwl#hasDbXref	チェディアック・東症候群	Chediak-Higashi syndrome	https://identifiers.org/kegg.disease:H02021
NANDO:2200725	http://nanbyodata.jp/ontology/NANDO_2200725	X連鎖リンパ増殖症候群	X-linked lymphoproliferative syndrome	H01969	http://www.geneontology.org/formats/oboInOwl#hasDbXref	Duncan 病	X-linked lymphoproliferative syndrome	https://identifiers.org/kegg.disease:H01969
NANDO:2200725	http://nanbyodata.jp/ontology/NANDO_2200725	X連鎖リンパ増殖症候群	X-linked lymphoproliferative syndrome	H01969	http://www.geneontology.org/formats/oboInOwl#hasDbXref	X連鎖性リンパ球増殖症候群	X-linked lymphoproliferative syndrome	https://identifiers.org/kegg.disease:H01969
NANDO:2200725	http://nanbyodata.jp/ontology/NANDO_2200725	X連鎖リンパ増殖症候群	X-linked lymphoproliferative syndrome	H01969	http://www.geneontology.org/formats/oboInOwl#hasDbXref	Duncan 病	Duncan disease	https://identifiers.org/kegg.disease:H01969
NANDO:2200725	http://nanbyodata.jp/ontology/NANDO_2200725	X連鎖リンパ増殖症候群	X-linked lymphoproliferative syndrome	H01969	http://www.geneontology.org/formats/oboInOwl#hasDbXref	X連鎖性リンパ球増殖症候群	Duncan disease	https://identifiers.org/kegg.disease:H01969
NANDO:2200758	http://nanbyodata.jp/ontology/NANDO_2200758	ミエロペルオキシダーゼ欠損症	Myeloperoxidase deficiency	H02025	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ミエロペルオキシダーゼ欠損症	Myeloperoxidase deficiency	https://identifiers.org/kegg.disease:H02025
NANDO:2200792	http://nanbyodata.jp/ontology/NANDO_2200792	3MC 症候群	Malpuech-Michels-Mingarelli-Carnevale syndrome	H01887	http://www.geneontology.org/formats/oboInOwl#hasDbXref	3MC 症候群	3MC syndrome	https://identifiers.org/kegg.disease:H01887
NANDO:2200792	http://nanbyodata.jp/ontology/NANDO_2200792	3MC 症候群	Malpuech-Michels-Mingarelli-Carnevale syndrome	H01887	http://www.geneontology.org/formats/oboInOwl#hasDbXref	3MC 症候群	Malpuech-Michels-Mingarelli-Carnevale syndrome	https://identifiers.org/kegg.disease:H01887
NANDO:2200823	http://nanbyodata.jp/ontology/NANDO_2200823	巨脳症－毛細血管奇形症候群	Megalencephaly-capillary malformation syndrome	H02153	http://www.geneontology.org/formats/oboInOwl#hasDbXref	MCAP 症候群	Megalencephaly-capillary malformation syndrome	https://identifiers.org/kegg.disease:H02153
NANDO:2200823	http://nanbyodata.jp/ontology/NANDO_2200823	巨脳症－毛細血管奇形症候群	Megalencephaly-capillary malformation syndrome	H02153	http://www.geneontology.org/formats/oboInOwl#hasDbXref	巨頭症-毛細血管奇形症候群	Megalencephaly-capillary malformation syndrome	https://identifiers.org/kegg.disease:H02153
NANDO:2200823	http://nanbyodata.jp/ontology/NANDO_2200823	巨脳症－毛細血管奇形症候群	Megalencephaly-capillary malformation syndrome	H02153	http://www.geneontology.org/formats/oboInOwl#hasDbXref	MCAP 症候群	MCAP syndrome	https://identifiers.org/kegg.disease:H02153
NANDO:2200823	http://nanbyodata.jp/ontology/NANDO_2200823	巨脳症－毛細血管奇形症候群	Megalencephaly-capillary malformation syndrome	H02153	http://www.geneontology.org/formats/oboInOwl#hasDbXref	巨頭症-毛細血管奇形症候群	MCAP syndrome	https://identifiers.org/kegg.disease:H02153
NANDO:2200847	http://nanbyodata.jp/ontology/NANDO_2200847	Carpenter症候群	Carpenter syndrome	H01888	http://www.geneontology.org/formats/oboInOwl#hasDbXref	カーペンター症候群	Carpenter syndrome	https://identifiers.org/kegg.disease:H01888
NANDO:2200848	http://nanbyodata.jp/ontology/NANDO_2200848	Seather-Chotzen症候群	Saethre-Chotzen syndrome	H01991	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ゼーツレ‐コッツェン症候群	Saethre-Chotzen syndrome	https://identifiers.org/kegg.disease:H01991
NANDO:2200856	http://nanbyodata.jp/ontology/NANDO_2200856	デュシェンヌ型筋ジストロフィー	Duchenne muscular dystrophy	H01963	http://www.geneontology.org/formats/oboInOwl#hasDbXref	デュシェンヌ型筋ジストロフィー	Duchenne muscular dystrophy	https://identifiers.org/kegg.disease:H01963
NANDO:2200860	http://nanbyodata.jp/ontology/NANDO_2200860	福山型先天性筋ジストロフィー	Fukuyama type congenital muscular dystrophy	H01957	http://www.geneontology.org/formats/oboInOwl#hasDbXref	福山型先天性筋ジストロフィー	Fukuyama congenital muscular dystrophy	https://identifiers.org/kegg.disease:H01957
NANDO:2200861	http://nanbyodata.jp/ontology/NANDO_2200861	メロシン欠損型先天性筋ジストロフィー	Merosin-deficient congenital muscular dystrophy	H01958	http://www.geneontology.org/formats/oboInOwl#hasDbXref	メロシン欠損型先天性筋ジストロフィー	Merosin-deficient congenital muscular dystrophy	https://identifiers.org/kegg.disease:H01958
NANDO:2200865	http://nanbyodata.jp/ontology/NANDO_2200865	ベッカー型筋ジストロフィー	Becker muscular dystrophy	H01964	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ベッカー型筋ジストロフィー	Becker muscular dystrophy	https://identifiers.org/kegg.disease:H01964
NANDO:2200880	http://nanbyodata.jp/ontology/NANDO_2200880	ウンフェルリヒト・ルントボルク病	Unverricht-Lundborg disease	H01995	http://www.geneontology.org/formats/oboInOwl#hasDbXref	Unverricht-Lundborg 病	Unverricht-Lundborg disease	https://identifiers.org/kegg.disease:H01995
NANDO:2200880	http://nanbyodata.jp/ontology/NANDO_2200880	ウンフェルリヒト・ルントボルク病	Unverricht-Lundborg disease	H01995	http://www.geneontology.org/formats/oboInOwl#hasDbXref	進行性ミオクローヌスてんかん 1 型	Unverricht-Lundborg disease	https://identifiers.org/kegg.disease:H01995
NANDO:2200880	http://nanbyodata.jp/ontology/NANDO_2200880	ウンフェルリヒト・ルントボルク病	Unverricht-Lundborg disease	H01995	http://www.geneontology.org/formats/oboInOwl#hasDbXref	Unverricht-Lundborg 病	Epilepsy, progressive myoclonic 1	https://identifiers.org/kegg.disease:H01995
NANDO:2200880	http://nanbyodata.jp/ontology/NANDO_2200880	ウンフェルリヒト・ルントボルク病	Unverricht-Lundborg disease	H01995	http://www.geneontology.org/formats/oboInOwl#hasDbXref	進行性ミオクローヌスてんかん 1 型	Epilepsy, progressive myoclonic 1	https://identifiers.org/kegg.disease:H01995
NANDO:2200881	http://nanbyodata.jp/ontology/NANDO_2200881	ラフォラ病	Lafora disease	H01994	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ラフォラ病	Lafora disease	https://identifiers.org/kegg.disease:H01994
NANDO:2200886	http://nanbyodata.jp/ontology/NANDO_2200886	パントテン酸キナーゼ関連神経変性症	Pantothenate kinase-associated neurodegeneration	H02208	http://www.geneontology.org/formats/oboInOwl#hasDbXref	パントテン酸キナーゼ関連神経変性症	Pantothenate kinase-associated neurodegeneration	https://identifiers.org/kegg.disease:H02208
NANDO:2200886	http://nanbyodata.jp/ontology/NANDO_2200886	パントテン酸キナーゼ関連神経変性症	Pantothenate kinase-associated neurodegeneration	H02208	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ハラーフォルデン・シュパッツ病	Pantothenate kinase-associated neurodegeneration	https://identifiers.org/kegg.disease:H02208
NANDO:2200886	http://nanbyodata.jp/ontology/NANDO_2200886	パントテン酸キナーゼ関連神経変性症	Pantothenate kinase-associated neurodegeneration	H02208	http://www.geneontology.org/formats/oboInOwl#hasDbXref	脳の鉄沈着を伴う神経変性症 1型	Pantothenate kinase-associated neurodegeneration	https://identifiers.org/kegg.disease:H02208
NANDO:2200886	http://nanbyodata.jp/ontology/NANDO_2200886	パントテン酸キナーゼ関連神経変性症	Pantothenate kinase-associated neurodegeneration	H02208	http://www.geneontology.org/formats/oboInOwl#hasDbXref	パントテン酸キナーゼ関連神経変性症	Hallervorden-Spatz disease	https://identifiers.org/kegg.disease:H02208
NANDO:2200886	http://nanbyodata.jp/ontology/NANDO_2200886	パントテン酸キナーゼ関連神経変性症	Pantothenate kinase-associated neurodegeneration	H02208	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ハラーフォルデン・シュパッツ病	Hallervorden-Spatz disease	https://identifiers.org/kegg.disease:H02208
NANDO:2200886	http://nanbyodata.jp/ontology/NANDO_2200886	パントテン酸キナーゼ関連神経変性症	Pantothenate kinase-associated neurodegeneration	H02208	http://www.geneontology.org/formats/oboInOwl#hasDbXref	脳の鉄沈着を伴う神経変性症 1型	Hallervorden-Spatz disease	https://identifiers.org/kegg.disease:H02208
NANDO:2200886	http://nanbyodata.jp/ontology/NANDO_2200886	パントテン酸キナーゼ関連神経変性症	Pantothenate kinase-associated neurodegeneration	H02208	http://www.geneontology.org/formats/oboInOwl#hasDbXref	パントテン酸キナーゼ関連神経変性症	Neurodegeneration with brain iron accumulation 1	https://identifiers.org/kegg.disease:H02208
NANDO:2200886	http://nanbyodata.jp/ontology/NANDO_2200886	パントテン酸キナーゼ関連神経変性症	Pantothenate kinase-associated neurodegeneration	H02208	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ハラーフォルデン・シュパッツ病	Neurodegeneration with brain iron accumulation 1	https://identifiers.org/kegg.disease:H02208
NANDO:2200886	http://nanbyodata.jp/ontology/NANDO_2200886	パントテン酸キナーゼ関連神経変性症	Pantothenate kinase-associated neurodegeneration	H02208	http://www.geneontology.org/formats/oboInOwl#hasDbXref	脳の鉄沈着を伴う神経変性症 1型	Neurodegeneration with brain iron accumulation 1	https://identifiers.org/kegg.disease:H02208
NANDO:2200924	http://nanbyodata.jp/ontology/NANDO_2200924	IPEX症候群	IPEX syndrome	H01971	http://www.geneontology.org/formats/oboInOwl#hasDbXref	IPEX 症候群	IPEX syndrome	https://identifiers.org/kegg.disease:H01971
NANDO:2200924	http://nanbyodata.jp/ontology/NANDO_2200924	IPEX症候群	IPEX syndrome	H01971	http://www.geneontology.org/formats/oboInOwl#hasDbXref	IPEX 症候群	Immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome	https://identifiers.org/kegg.disease:H01971
NANDO:2200941	http://nanbyodata.jp/ontology/NANDO_2200941	クリグラー・ナジャー症候群	Crigler-Najjar syndrome	H02054	http://www.geneontology.org/formats/oboInOwl#hasDbXref	クリグラー・ナジャー症候群	Crigler-Najjar syndrome	https://identifiers.org/kegg.disease:H02054
NANDO:2200947	http://nanbyodata.jp/ontology/NANDO_2200947	巨大膀胱短小結腸腸管蠕動不全症	Megacystis-microcolon-intestinal hypoperistalsis syndrome	H01869	http://www.geneontology.org/formats/oboInOwl#hasDbXref	巨大膀胱短小結腸腸管蠕動不全症	Megacystis microcolon intestinal hypoperistalsis syndrome	https://identifiers.org/kegg.disease:H01869
NANDO:2200948	http://nanbyodata.jp/ontology/NANDO_2200948	腸管神経節細胞僅少症	Congenital Isolated Hypoganglionosis	H01871	http://www.geneontology.org/formats/oboInOwl#hasDbXref	腸管神経節細胞僅少症	Isolated hypoganglionosis	https://identifiers.org/kegg.disease:H01871
NANDO:2200950	http://nanbyodata.jp/ontology/NANDO_2200950	総排泄腔遺残	Persistent cloaca	H01858	http://www.geneontology.org/formats/oboInOwl#hasDbXref	総排泄腔遺残	Persistent cloaca	https://identifiers.org/kegg.disease:H01858
NANDO:2201010	http://nanbyodata.jp/ontology/NANDO_2201010	軟骨低形成症	Hypochondroplasia	H02068	http://www.geneontology.org/formats/oboInOwl#hasDbXref	軟骨低形成症	Hypochondroplasia	https://identifiers.org/kegg.disease:H02068
NANDO:2201019	http://nanbyodata.jp/ontology/NANDO_2201019	ラーセン症候群	Larsen syndrome	H02048	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ラーセン症候群	Larsen syndrome	https://identifiers.org/kegg.disease:H02048
NANDO:2201067	http://nanbyodata.jp/ontology/NANDO_2201067	マックル・ウェルズ症候群	Muckle-Wells syndrome	H02555	http://www.geneontology.org/formats/oboInOwl#hasDbXref	マックル-ウェルズ症候群	Muckle-Wells syndrome	https://identifiers.org/kegg.disease:H02555
NANDO:2201068	http://nanbyodata.jp/ontology/NANDO_2201068	家族性寒冷自己炎症症候群	familial cold autoinflammatory syndrome	H02159	http://www.geneontology.org/formats/oboInOwl#hasDbXref	家族性寒冷自己炎症症候群	Familial cold autoinflammatory syndrome	https://identifiers.org/kegg.disease:H02159
NANDO:2201068	http://nanbyodata.jp/ontology/NANDO_2201068	家族性寒冷自己炎症症候群	familial cold autoinflammatory syndrome	H02159	http://www.geneontology.org/formats/oboInOwl#hasDbXref	家族性寒冷じんま疹	Familial cold autoinflammatory syndrome	https://identifiers.org/kegg.disease:H02159
NANDO:2201068	http://nanbyodata.jp/ontology/NANDO_2201068	家族性寒冷自己炎症症候群	familial cold autoinflammatory syndrome	H02159	http://www.geneontology.org/formats/oboInOwl#hasDbXref	家族性寒冷自己炎症症候群	Familial cold urticaria	https://identifiers.org/kegg.disease:H02159
NANDO:2201068	http://nanbyodata.jp/ontology/NANDO_2201068	家族性寒冷自己炎症症候群	familial cold autoinflammatory syndrome	H02159	http://www.geneontology.org/formats/oboInOwl#hasDbXref	家族性寒冷じんま疹	Familial cold urticaria	https://identifiers.org/kegg.disease:H02159
NANDO:2201151	http://nanbyodata.jp/ontology/NANDO_2201151	糖原病0a型	Glycogen storage disease type 0a	H01950	http://www.geneontology.org/formats/oboInOwl#hasDbXref	糖原病 0a 型	Glycogen storage disease type 0a	https://identifiers.org/kegg.disease:H01950
NANDO:2201151	http://nanbyodata.jp/ontology/NANDO_2201151	糖原病0a型	Glycogen storage disease type 0a	H01950	http://www.geneontology.org/formats/oboInOwl#hasDbXref	肝グリコーゲン合成酵素欠損症	Glycogen storage disease type 0a	https://identifiers.org/kegg.disease:H01950
NANDO:2201151	http://nanbyodata.jp/ontology/NANDO_2201151	糖原病0a型	Glycogen storage disease type 0a	H01950	http://www.geneontology.org/formats/oboInOwl#hasDbXref	糖原病 0a 型	Liver glycogen synthase deficiency	https://identifiers.org/kegg.disease:H01950
NANDO:2201151	http://nanbyodata.jp/ontology/NANDO_2201151	糖原病0a型	Glycogen storage disease type 0a	H01950	http://www.geneontology.org/formats/oboInOwl#hasDbXref	肝グリコーゲン合成酵素欠損症	Liver glycogen synthase deficiency	https://identifiers.org/kegg.disease:H01950
NANDO:2201152	http://nanbyodata.jp/ontology/NANDO_2201152	糖原病0b型	Glycogen storage disease type 0b	H01949	http://www.geneontology.org/formats/oboInOwl#hasDbXref	筋グリコーゲン合成酵素欠損症	Glycogen storage disease type 0b	https://identifiers.org/kegg.disease:H01949
NANDO:2201152	http://nanbyodata.jp/ontology/NANDO_2201152	糖原病0b型	Glycogen storage disease type 0b	H01949	http://www.geneontology.org/formats/oboInOwl#hasDbXref	糖原病 0b 型	Glycogen storage disease type 0b	https://identifiers.org/kegg.disease:H01949
NANDO:2201152	http://nanbyodata.jp/ontology/NANDO_2201152	糖原病0b型	Glycogen storage disease type 0b	H01949	http://www.geneontology.org/formats/oboInOwl#hasDbXref	筋グリコーゲン合成酵素欠損症	Muscle glycogen synthase deficiency	https://identifiers.org/kegg.disease:H01949
NANDO:2201152	http://nanbyodata.jp/ontology/NANDO_2201152	糖原病0b型	Glycogen storage disease type 0b	H01949	http://www.geneontology.org/formats/oboInOwl#hasDbXref	糖原病 0b 型	Muscle glycogen synthase deficiency	https://identifiers.org/kegg.disease:H01949
NANDO:2201199	http://nanbyodata.jp/ontology/NANDO_2201199	テイ・サックス病	Tay-Sachs disease	H02016	http://www.geneontology.org/formats/oboInOwl#hasDbXref	テイ・サックス病	Tay-Sachs disease	https://identifiers.org/kegg.disease:H02016
NANDO:2201199	http://nanbyodata.jp/ontology/NANDO_2201199	テイ・サックス病	Tay-Sachs disease	H02016	http://www.geneontology.org/formats/oboInOwl#hasDbXref	GM2 ガングリオシドーシス I 型	Tay-Sachs disease	https://identifiers.org/kegg.disease:H02016
NANDO:2201199	http://nanbyodata.jp/ontology/NANDO_2201199	テイ・サックス病	Tay-Sachs disease	H02016	http://www.geneontology.org/formats/oboInOwl#hasDbXref	テイ・サックス病	GM2 gangliosidoses type I	https://identifiers.org/kegg.disease:H02016
NANDO:2201199	http://nanbyodata.jp/ontology/NANDO_2201199	テイ・サックス病	Tay-Sachs disease	H02016	http://www.geneontology.org/formats/oboInOwl#hasDbXref	GM2 ガングリオシドーシス I 型	GM2 gangliosidoses type I	https://identifiers.org/kegg.disease:H02016
NANDO:2201200	http://nanbyodata.jp/ontology/NANDO_2201200	サンドホフ病	Sandhoff disease	H02017	http://www.geneontology.org/formats/oboInOwl#hasDbXref	サンドホフ病	Sandhoff disease	https://identifiers.org/kegg.disease:H02017
NANDO:2201200	http://nanbyodata.jp/ontology/NANDO_2201200	サンドホフ病	Sandhoff disease	H02017	http://www.geneontology.org/formats/oboInOwl#hasDbXref	GM2 ガングリオシドーシス II 型	Sandhoff disease	https://identifiers.org/kegg.disease:H02017
NANDO:2201200	http://nanbyodata.jp/ontology/NANDO_2201200	サンドホフ病	Sandhoff disease	H02017	http://www.geneontology.org/formats/oboInOwl#hasDbXref	サンドホフ病	GM2 gangliosidoses type II	https://identifiers.org/kegg.disease:H02017
NANDO:2201200	http://nanbyodata.jp/ontology/NANDO_2201200	サンドホフ病	Sandhoff disease	H02017	http://www.geneontology.org/formats/oboInOwl#hasDbXref	GM2 ガングリオシドーシス II 型	GM2 gangliosidoses type II	https://identifiers.org/kegg.disease:H02017
NANDO:2201241	http://nanbyodata.jp/ontology/NANDO_2201241	乳児型神経セロイドリポフスチン症	Infantile neuronal ceroid lipofuscinosis	H02277	http://www.geneontology.org/formats/oboInOwl#hasDbXref	乳児型神経セロイドリポフスチン症	Infantile neuronal ceroid lipofuscinosis	https://identifiers.org/kegg.disease:H02277
NANDO:2201241	http://nanbyodata.jp/ontology/NANDO_2201241	乳児型神経セロイドリポフスチン症	Infantile neuronal ceroid lipofuscinosis	H02277	http://www.geneontology.org/formats/oboInOwl#hasDbXref	Santavuori-Haltia 病	Infantile neuronal ceroid lipofuscinosis	https://identifiers.org/kegg.disease:H02277
NANDO:2201241	http://nanbyodata.jp/ontology/NANDO_2201241	乳児型神経セロイドリポフスチン症	Infantile neuronal ceroid lipofuscinosis	H02277	http://www.geneontology.org/formats/oboInOwl#hasDbXref	乳児型神経セロイドリポフスチン症	Santavuori-Haltia disease	https://identifiers.org/kegg.disease:H02277
NANDO:2201241	http://nanbyodata.jp/ontology/NANDO_2201241	乳児型神経セロイドリポフスチン症	Infantile neuronal ceroid lipofuscinosis	H02277	http://www.geneontology.org/formats/oboInOwl#hasDbXref	Santavuori-Haltia 病	Santavuori-Haltia disease	https://identifiers.org/kegg.disease:H02277
NANDO:2201243	http://nanbyodata.jp/ontology/NANDO_2201243	若年型神経セロイドリポフスチン症	Juvenile neuronal ceroid lipofuscinosis	H02275	http://www.geneontology.org/formats/oboInOwl#hasDbXref	若年型神経セロイドリポフスチン症	Batten disease	https://identifiers.org/kegg.disease:H02275
NANDO:2201243	http://nanbyodata.jp/ontology/NANDO_2201243	若年型神経セロイドリポフスチン症	Juvenile neuronal ceroid lipofuscinosis	H02275	http://www.geneontology.org/formats/oboInOwl#hasDbXref	Spielmeyer-Vogt 病	Batten disease	https://identifiers.org/kegg.disease:H02275
NANDO:2201243	http://nanbyodata.jp/ontology/NANDO_2201243	若年型神経セロイドリポフスチン症	Juvenile neuronal ceroid lipofuscinosis	H02275	http://www.geneontology.org/formats/oboInOwl#hasDbXref	バッテン病	Batten disease	https://identifiers.org/kegg.disease:H02275
NANDO:2201243	http://nanbyodata.jp/ontology/NANDO_2201243	若年型神経セロイドリポフスチン症	Juvenile neuronal ceroid lipofuscinosis	H02275	http://www.geneontology.org/formats/oboInOwl#hasDbXref	若年型神経セロイドリポフスチン症	Juvenile neuronal ceroid lipofuscinoses	https://identifiers.org/kegg.disease:H02275
NANDO:2201243	http://nanbyodata.jp/ontology/NANDO_2201243	若年型神経セロイドリポフスチン症	Juvenile neuronal ceroid lipofuscinosis	H02275	http://www.geneontology.org/formats/oboInOwl#hasDbXref	Spielmeyer-Vogt 病	Juvenile neuronal ceroid lipofuscinoses	https://identifiers.org/kegg.disease:H02275
NANDO:2201243	http://nanbyodata.jp/ontology/NANDO_2201243	若年型神経セロイドリポフスチン症	Juvenile neuronal ceroid lipofuscinosis	H02275	http://www.geneontology.org/formats/oboInOwl#hasDbXref	バッテン病	Juvenile neuronal ceroid lipofuscinoses	https://identifiers.org/kegg.disease:H02275
NANDO:2201243	http://nanbyodata.jp/ontology/NANDO_2201243	若年型神経セロイドリポフスチン症	Juvenile neuronal ceroid lipofuscinosis	H02275	http://www.geneontology.org/formats/oboInOwl#hasDbXref	若年型神経セロイドリポフスチン症	Spielmeyer-Vogt disease	https://identifiers.org/kegg.disease:H02275
NANDO:2201243	http://nanbyodata.jp/ontology/NANDO_2201243	若年型神経セロイドリポフスチン症	Juvenile neuronal ceroid lipofuscinosis	H02275	http://www.geneontology.org/formats/oboInOwl#hasDbXref	Spielmeyer-Vogt 病	Spielmeyer-Vogt disease	https://identifiers.org/kegg.disease:H02275
NANDO:2201243	http://nanbyodata.jp/ontology/NANDO_2201243	若年型神経セロイドリポフスチン症	Juvenile neuronal ceroid lipofuscinosis	H02275	http://www.geneontology.org/formats/oboInOwl#hasDbXref	バッテン病	Spielmeyer-Vogt disease	https://identifiers.org/kegg.disease:H02275
NANDO:2201244	http://nanbyodata.jp/ontology/NANDO_2201244	成人型神経セロイドリポフスチン症	Adult neuronal ceroid lipofuscinosis	H02276	http://www.geneontology.org/formats/oboInOwl#hasDbXref	成人型神経セロイドリポフスチン症	Kufs disease	https://identifiers.org/kegg.disease:H02276
NANDO:2201244	http://nanbyodata.jp/ontology/NANDO_2201244	成人型神経セロイドリポフスチン症	Adult neuronal ceroid lipofuscinosis	H02276	http://www.geneontology.org/formats/oboInOwl#hasDbXref	Kufs 病	Kufs disease	https://identifiers.org/kegg.disease:H02276
NANDO:2201244	http://nanbyodata.jp/ontology/NANDO_2201244	成人型神経セロイドリポフスチン症	Adult neuronal ceroid lipofuscinosis	H02276	http://www.geneontology.org/formats/oboInOwl#hasDbXref	成人型神経セロイドリポフスチン症	Adult-onset neuronal ceroid lipofuscinosis	https://identifiers.org/kegg.disease:H02276
NANDO:2201244	http://nanbyodata.jp/ontology/NANDO_2201244	成人型神経セロイドリポフスチン症	Adult neuronal ceroid lipofuscinosis	H02276	http://www.geneontology.org/formats/oboInOwl#hasDbXref	Kufs 病	Adult-onset neuronal ceroid lipofuscinosis	https://identifiers.org/kegg.disease:H02276
NANDO:2201350	http://nanbyodata.jp/ontology/NANDO_2201350	Kniest異形成症	Kniest dysplasia	H02070	http://www.geneontology.org/formats/oboInOwl#hasDbXref	Kniest 異形成症	Kniest dysplasia	https://identifiers.org/kegg.disease:H02070
NANDO:2201364	http://nanbyodata.jp/ontology/NANDO_2201364	流蝋骨症	Melorheostosis	H02631	http://www.geneontology.org/formats/oboInOwl#hasDbXref	メロレオストーシス	Melorheostosis	https://identifiers.org/kegg.disease:H02631
NANDO:2201364	http://nanbyodata.jp/ontology/NANDO_2201364	流蝋骨症	Melorheostosis	H02631	http://www.geneontology.org/formats/oboInOwl#hasDbXref	流蝋骨症	Melorheostosis	https://identifiers.org/kegg.disease:H02631
NANDO:2201417	http://nanbyodata.jp/ontology/NANDO_2201417	ヴィーデマン・スタイナー症候群	Wiedemann-Steiner syndrome	H01879	http://www.geneontology.org/formats/oboInOwl#hasDbXref	Alazami-Yuan 症候群	Wiedemann-Steiner syndrome	https://identifiers.org/kegg.disease:H01879
NANDO:2201417	http://nanbyodata.jp/ontology/NANDO_2201417	ヴィーデマン・スタイナー症候群	Wiedemann-Steiner syndrome	H01879	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ウィデマンスタイナー症候群	Wiedemann-Steiner syndrome	https://identifiers.org/kegg.disease:H01879
NANDO:2201417	http://nanbyodata.jp/ontology/NANDO_2201417	ヴィーデマン・スタイナー症候群	Wiedemann-Steiner syndrome	H01879	http://www.geneontology.org/formats/oboInOwl#hasDbXref	Alazami-Yuan 症候群	Alazami-Yuan syndrome	https://identifiers.org/kegg.disease:H01879
NANDO:2201417	http://nanbyodata.jp/ontology/NANDO_2201417	ヴィーデマン・スタイナー症候群	Wiedemann-Steiner syndrome	H01879	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ウィデマンスタイナー症候群	Alazami-Yuan syndrome	https://identifiers.org/kegg.disease:H01879
NANDO:2201525	http://nanbyodata.jp/ontology/NANDO_2201525	シャーフ・ヤング症候群	Schaaf-Yang syndrome	H02325	http://www.geneontology.org/formats/oboInOwl#hasDbXref	Schaaf-Yang 症候群	Schaaf-Yang syndrome	https://identifiers.org/kegg.disease:H02325
NANDO:1201152	http://nanbyodata.jp/ontology/NANDO_1201152	無セルロプラスミン血症	Aceruloplasminemia	H02206	http://www.geneontology.org/formats/oboInOwl#hasDbXref	無セルロプラスミン血症	Aceruloplasminemia	https://identifiers.org/kegg.disease:H02206
NANDO:1201152	http://nanbyodata.jp/ontology/NANDO_1201152	無セルロプラスミン血症	Aceruloplasminemia	H02206	http://www.geneontology.org/formats/oboInOwl#hasDbXref	セルロプラスミン欠損症	Aceruloplasminemia	https://identifiers.org/kegg.disease:H02206
NANDO:1201152	http://nanbyodata.jp/ontology/NANDO_1201152	無セルロプラスミン血症	Aceruloplasminemia	H02206	http://www.geneontology.org/formats/oboInOwl#hasDbXref	無セルロプラスミン血症	Ceruloplasmin deficiency	https://identifiers.org/kegg.disease:H02206
NANDO:1201152	http://nanbyodata.jp/ontology/NANDO_1201152	無セルロプラスミン血症	Aceruloplasminemia	H02206	http://www.geneontology.org/formats/oboInOwl#hasDbXref	セルロプラスミン欠損症	Ceruloplasmin deficiency	https://identifiers.org/kegg.disease:H02206
NANDO:1201175	http://nanbyodata.jp/ontology/NANDO_1201175	ホスホリラーゼキナーゼ欠損症	Phosphorylase kinase deficiency	H01948	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ホスホリラーゼキナーゼ欠損症	Glycogen storage disease type IX	https://identifiers.org/kegg.disease:H01948
NANDO:1201175	http://nanbyodata.jp/ontology/NANDO_1201175	ホスホリラーゼキナーゼ欠損症	Phosphorylase kinase deficiency	H01948	http://www.geneontology.org/formats/oboInOwl#hasDbXref	糖原病 IX 型	Glycogen storage disease type IX	https://identifiers.org/kegg.disease:H01948
NANDO:1201175	http://nanbyodata.jp/ontology/NANDO_1201175	ホスホリラーゼキナーゼ欠損症	Phosphorylase kinase deficiency	H01948	http://www.geneontology.org/formats/oboInOwl#hasDbXref	ホスホリラーゼキナーゼ欠損症	Phosphorylase kinase deficiency	https://identifiers.org/kegg.disease:H01948
NANDO:1201175	http://nanbyodata.jp/ontology/NANDO_1201175	ホスホリラーゼキナーゼ欠損症	Phosphorylase kinase deficiency	H01948	http://www.geneontology.org/formats/oboInOwl#hasDbXref	糖原病 IX 型	Phosphorylase kinase deficiency	https://identifiers.org/kegg.disease:H01948
NANDO:1200483	http://nanbyodata.jp/ontology/NANDO_1200483	先天性筋線維タイプ不均等症	Congenital fiber-type disproportion myopathy	H00701	http://www.geneontology.org/formats/oboInOwl#hasDbXref	先天性筋線維タイプ不均等症	Congenital fiber type disproportion	https://identifiers.org/kegg.disease:H00701
NANDO:1201154	http://nanbyodata.jp/ontology/NANDO_1201154	Woodhouse-Sakati症候群	Woodhouse-Sakati syndrome	H00682	http://www.geneontology.org/formats/oboInOwl#hasDbXref	Woodhouse-Sakati 症候群	Woodhouse-Sakati syndrome	https://identifiers.org/kegg.disease:H00682
NANDO:1201154	http://nanbyodata.jp/ontology/NANDO_1201154	Woodhouse-Sakati症候群	Woodhouse-Sakati syndrome	H00682	http://www.geneontology.org/formats/oboInOwl#hasDbXref	Woodhouse-Sakati 症候群	Hypogonadism, alopecia, diabetes mellitus, mental retardation, and extrapyramidal syndrome	https://identifiers.org/kegg.disease:H00682
NANDO:1200315	http://nanbyodata.jp/ontology/NANDO_1200315	免疫性血小板減少症	Immune thrombocytopenia	H01240	http://www.geneontology.org/formats/oboInOwl#hasDbXref	自己免疫性血小板減少性紫斑病	Immune thrombocytopenia	https://identifiers.org/kegg.disease:H01240
NANDO:1200315	http://nanbyodata.jp/ontology/NANDO_1200315	免疫性血小板減少症	Immune thrombocytopenia	H01240	http://www.geneontology.org/formats/oboInOwl#hasDbXref	自己免疫性血小板減少性紫斑病	Autoimmune thrombocytopenic purpura	https://identifiers.org/kegg.disease:H01240
NANDO:1201153	http://nanbyodata.jp/ontology/NANDO_1201153	Kufor-Rakeb症候群	Kufor-Rakeb syndrome	H02207	http://www.geneontology.org/formats/oboInOwl#hasDbXref	Kufor-Rakeb 症候群	Kufor-Rakeb syndrome	https://identifiers.org/kegg.disease:H02207
NANDO:1201153	http://nanbyodata.jp/ontology/NANDO_1201153	Kufor-Rakeb症候群	Kufor-Rakeb syndrome	H02207	http://www.geneontology.org/formats/oboInOwl#hasDbXref	パーキンソン病 9 型	Parkinson disease 9	https://identifiers.org/kegg.disease:H02207
NANDO:1201153	http://nanbyodata.jp/ontology/NANDO_1201153	Kufor-Rakeb症候群	Kufor-Rakeb syndrome	H02207	http://www.geneontology.org/formats/oboInOwl#hasDbXref	パーキンソン病 9 型	Kufor-Rakeb syndrome	https://identifiers.org/kegg.disease:H02207
NANDO:1201153	http://nanbyodata.jp/ontology/NANDO_1201153	Kufor-Rakeb症候群	Kufor-Rakeb syndrome	H02207	http://www.geneontology.org/formats/oboInOwl#hasDbXref	Kufor-Rakeb 症候群	Parkinson disease 9	https://identifiers.org/kegg.disease:H02207