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    "nando_id": "NANDO:1200714",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200714",
    "nando_label_ja": "急速進行性糸球体腎炎",
    "nando_label_en": "Rapidly progressive glomerulonephritis",
    "mondo_id": "MONDO:0001645",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_label_ja": "半月体形成性糸球体腎炎",
    "mondo_label_en": "crescentic glomerulonephritis",
    "mondo_url": "https://monarchinitiative.org/MONDO:0001645"
  },
  {
    "nando_id": "NANDO:1200482",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200482",
    "nando_label_ja": "中心核ミオパチー",
    "nando_label_en": "Centronuclear myopathy",
    "mondo_id": "MONDO:0002921",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_label_ja": "先天性構造ミオパチー",
    "mondo_label_en": "congenital structural myopathy",
    "mondo_url": "https://monarchinitiative.org/MONDO:0002921"
  },
  {
    "nando_id": "NANDO:1200173",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200173",
    "nando_label_ja": "ミトコンドリア病",
    "nando_label_en": "Mitochondrial diseases",
    "mondo_id": "MONDO:0004069",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_label_ja": "先天性ミトコンドリア代謝障害",
    "mondo_label_en": "inborn mitochondrial metabolism disorder",
    "mondo_url": "https://monarchinitiative.org/MONDO:0004069"
  },
  {
    "nando_id": "NANDO:1200446",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200446",
    "nando_label_ja": "大腸型クローン病",
    "nando_label_en": "Colonic Crohn's disease",
    "mondo_id": "MONDO:0005011",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_label_ja": "クローン病",
    "mondo_label_en": "Crohn disease",
    "mondo_url": "https://monarchinitiative.org/MONDO:0005011"
  },
  {
    "nando_id": "NANDO:1200288",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200288",
    "nando_label_ja": "閉塞性肥大型心筋症",
    "nando_label_en": "Hypertrophic obstructive cardiomyopathy",
    "mondo_id": "MONDO:0005045",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_label_ja": "肥大型心筋症",
    "mondo_label_en": "hypertrophic cardiomyopathy",
    "mondo_url": "https://monarchinitiative.org/MONDO:0005045"
  },
  {
    "nando_id": "NANDO:1200293",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200293",
    "nando_label_ja": "特発性拘束型心筋症",
    "nando_label_en": "Idiopathic restrictive cardiomyopathy",
    "mondo_id": "MONDO:0005201",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_label_ja": "拘束型心筋症",
    "mondo_label_en": "restrictive cardiomyopathy",
    "mondo_url": "https://monarchinitiative.org/MONDO:0005201"
  },
  {
    "nando_id": "NANDO:1200668",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200668",
    "nando_label_ja": "ファイファー症候群",
    "nando_label_en": "Pfeiffer syndrome",
    "mondo_id": "MONDO:0005810",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_label_ja": "伝染性単核症",
    "mondo_label_en": "infectious mononucleosis",
    "mondo_url": "https://monarchinitiative.org/MONDO:0005810"
  },
  {
    "nando_id": "NANDO:1200385",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200385",
    "nando_label_ja": "下垂体ゴナドトロピン産生腫瘍",
    "nando_label_en": "Growth hormone secreting pituitary adenoma",
    "mondo_id": "MONDO:0006238",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_label_ja": "成長ホルモン産生性下垂体腺腫",
    "mondo_label_en": "growth hormone-producing pituitary gland adenoma",
    "mondo_url": "https://monarchinitiative.org/MONDO:0006238"
  },
  {
    "nando_id": "NANDO:1200386",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200386",
    "nando_label_ja": "下垂体性成長ホルモン分泌亢進症",
    "nando_label_en": "Diencephalo-hypophysial dysfunction-syndrome of abnormal secretion of growth hormone",
    "mondo_id": "MONDO:0006238",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_label_ja": "成長ホルモン産生性下垂体腺腫",
    "mondo_label_en": "growth hormone-producing pituitary gland adenoma",
    "mondo_url": "https://monarchinitiative.org/MONDO:0006238"
  },
  {
    "nando_id": "NANDO:1200251",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200251",
    "nando_label_ja": "高安動脈炎",
    "nando_label_en": "Takayasu arteritis",
    "mondo_id": "MONDO:0006656",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_label_ja": "大動脈炎",
    "mondo_label_en": "aortitis",
    "mondo_url": "https://monarchinitiative.org/MONDO:0006656"
  },
  {
    "nando_id": "NANDO:1200214",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200214",
    "nando_label_ja": "遺伝性トランスサイレチンアミロイドーシス",
    "nando_label_en": "Hereditary Transthyretin Amyloidosis",
    "mondo_id": "MONDO:0007100",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_label_ja": "家族性アミロイドニューロパチー",
    "mondo_label_en": "familial amyloid neuropathy",
    "mondo_url": "https://monarchinitiative.org/MONDO:0007100"
  },
  {
    "nando_id": "NANDO:1200365",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200365",
    "nando_label_ja": "遺伝性血管性浮腫",
    "nando_label_en": "Hereditary angioedema",
    "mondo_id": "MONDO:0007361",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_label_ja": "C1抑制因子欠乏症",
    "mondo_label_en": "C1 inhibitor deficiency",
    "mondo_url": "https://monarchinitiative.org/MONDO:0007361"
  },
  {
    "nando_id": "NANDO:1200516",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200516",
    "nando_label_ja": "DYT5aジストニア",
    "nando_label_en": "Dystonia 5a",
    "mondo_id": "MONDO:0007495",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_label_ja": "ジストニア5",
    "mondo_label_en": "dystonia 5",
    "mondo_url": "https://monarchinitiative.org/MONDO:0007495"
  },
  {
    "nando_id": "NANDO:1200524",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200524",
    "nando_label_ja": "急性発症ジストニア・パーキンソニズム",
    "nando_label_en": "Rapid-onset dystonia-parkinsonism",
    "mondo_id": "MONDO:0007496",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_label_ja": "ジストニア12",
    "mondo_label_en": "dystonia 12",
    "mondo_url": "https://monarchinitiative.org/MONDO:0007496"
  },
  {
    "nando_id": "NANDO:1200030",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200030",
    "nando_label_ja": "慢性炎症性脱髄性多発神経炎",
    "nando_label_en": "Chronic inflammatory demyelinating polyneuropathy",
    "mondo_id": "MONDO:0007691",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_label_ja": "ギラン・バレー症候群, 家族性",
    "mondo_label_en": "Guillain-Barre syndrome, familial",
    "mondo_url": "https://monarchinitiative.org/MONDO:0007691"
  },
  {
    "nando_id": "NANDO:1200218",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200218",
    "nando_label_ja": "縁取り空胞を伴う遠位型ミオパチー",
    "nando_label_en": "Distal myopathy with rimmed vacuoles",
    "mondo_id": "MONDO:0007827",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_label_ja": "封入体筋炎",
    "mondo_label_en": "inclusion body myositis",
    "mondo_url": "https://monarchinitiative.org/MONDO:0007827"
  },
  {
    "nando_id": "NANDO:1200560",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200560",
    "nando_label_ja": "中隔視神経形成異常症／ドモルシア症候群",
    "nando_label_en": "Septo-optic dysplasia / De Morsier syndrome",
    "mondo_id": "MONDO:0008428",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_label_ja": "中隔視神経形成異常症",
    "mondo_label_en": "septooptic dysplasia",
    "mondo_url": "https://monarchinitiative.org/MONDO:0008428"
  },
  {
    "nando_id": "NANDO:1200339",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200339",
    "nando_label_ja": "胸腺低形成",
    "nando_label_en": "Thymus hypoplasia",
    "mondo_id": "MONDO:0008564",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_label_ja": "ディジョージ症候群",
    "mondo_label_en": "DiGeorge syndrome",
    "mondo_url": "https://monarchinitiative.org/MONDO:0008564"
  },
  {
    "nando_id": "NANDO:1200688",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200688",
    "nando_label_ja": "22q11.2欠失症候群",
    "nando_label_en": "22q11.2 deletion syndrome",
    "mondo_id": "MONDO:0008564",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_label_ja": "ディジョージ症候群",
    "mondo_label_en": "DiGeorge syndrome",
    "mondo_url": "https://monarchinitiative.org/MONDO:0008564"
  },
  {
    "nando_id": "NANDO:1200339",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200339",
    "nando_label_ja": "胸腺低形成",
    "nando_label_en": "Thymus hypoplasia",
    "mondo_id": "MONDO:0008644",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_label_ja": "口蓋帆・心臓・顔症候群",
    "mondo_label_en": "velocardiofacial syndrome",
    "mondo_url": "https://monarchinitiative.org/MONDO:0008644"
  },
  {
    "nando_id": "NANDO:1200688",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200688",
    "nando_label_ja": "22q11.2欠失症候群",
    "nando_label_en": "22q11.2 deletion syndrome",
    "mondo_id": "MONDO:0008644",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_label_ja": "口蓋帆・心臓・顔症候群",
    "mondo_label_en": "velocardiofacial syndrome",
    "mondo_url": "https://monarchinitiative.org/MONDO:0008644"
  },
  {
    "nando_id": "NANDO:1200153",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200153",
    "nando_label_ja": "遅発乳児型神経セロイドリポフスチン症",
    "nando_label_en": "Late infantile neuronal ceroid lipofuscinosis",
    "mondo_id": "MONDO:0008769",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_label_ja": "神経セロイドリポフスチン症2",
    "mondo_label_en": "neuronal ceroid lipofuscinosis 2",
    "mondo_url": "https://monarchinitiative.org/MONDO:0008769"
  },
  {
    "nando_id": "NANDO:1200138",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200138",
    "nando_label_ja": "ポンペ病",
    "nando_label_en": "Pompe disease",
    "mondo_id": "MONDO:0009290",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_label_ja": "糖原病II",
    "mondo_label_en": "glycogen storage disease II",
    "mondo_url": "https://monarchinitiative.org/MONDO:0009290"
  },
  {
    "nando_id": "NANDO:1200717",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200717",
    "nando_label_ja": "急速進行性糸球体腎炎（抗GBM抗体陽性）",
    "nando_label_en": "Anti-GBM rapidly progressive glomerulonephritis",
    "mondo_id": "MONDO:0009303",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_label_ja": "抗糸球体基底膜抗体症",
    "mondo_label_en": "anti-glomerular basement membrane disease",
    "mondo_url": "https://monarchinitiative.org/MONDO:0009303"
  },
  {
    "nando_id": "NANDO:1200109",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200109",
    "nando_label_ja": "マロトー・ラミー症候群（重症型）",
    "nando_label_en": "Maroteaux Lamy syndrome, rapidly progressing form",
    "mondo_id": "MONDO:0009661",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_label_ja": "ムコ多糖症6型",
    "mondo_label_en": "mucopolysaccharidosis type 6",
    "mondo_url": "https://monarchinitiative.org/MONDO:0009661"
  },
  {
    "nando_id": "NANDO:1200110",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200110",
    "nando_label_ja": "マロトー・ラミー症候群（軽症型）",
    "nando_label_en": "Maroteaux Lamy syndrome, slowly progressing form",
    "mondo_id": "MONDO:0009661",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_label_ja": "ムコ多糖症6型",
    "mondo_label_en": "mucopolysaccharidosis type 6",
    "mondo_url": "https://monarchinitiative.org/MONDO:0009661"
  },
  {
    "nando_id": "NANDO:1200215",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200215",
    "nando_label_ja": "ウルリッヒ病",
    "nando_label_en": "Ullrich disease",
    "mondo_id": "MONDO:0009681",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_label_ja": "ウルリッヒ型先天性筋ジストロフィー1A",
    "mondo_label_en": "Ullrich congenital muscular dystrophy 1A",
    "mondo_url": "https://monarchinitiative.org/MONDO:0009681"
  },
  {
    "nando_id": "NANDO:1200498",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200498",
    "nando_label_ja": "トムゼン病",
    "nando_label_en": "Thomsen disease",
    "mondo_id": "MONDO:0009710",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_label_ja": "トムゼン・ベッカー病",
    "mondo_label_en": "Thomsen and Becker disease",
    "mondo_url": "https://monarchinitiative.org/MONDO:0009710"
  },
  {
    "nando_id": "NANDO:1200120",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200120",
    "nando_label_ja": "新生児及び早期乳児型ガラクトシアリドーシス",
    "nando_label_en": "Galactosialidosis, early infantile form",
    "mondo_id": "MONDO:0009738",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_label_ja": "シアリドーシス2型",
    "mondo_label_en": "sialidosis type 2",
    "mondo_url": "https://monarchinitiative.org/MONDO:0009738"
  },
  {
    "nando_id": "NANDO:1200152",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200152",
    "nando_label_ja": "乳児型神経セロイドリポフスチン症",
    "nando_label_en": "Infantile neuronal ceroid lipofuscinosis",
    "mondo_id": "MONDO:0009744",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_label_ja": "神経セロイドリポフスチン症1",
    "mondo_label_en": "neuronal ceroid lipofuscinosis 1",
    "mondo_url": "https://monarchinitiative.org/MONDO:0009744"
  },
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    "nando_id": "NANDO:1200196",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200196",
    "nando_label_ja": "亜急性硬化性全脳炎（典型）",
    "nando_label_en": "Typical subacute sclerosing panencephalitis",
    "mondo_id": "MONDO:0009835",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_label_ja": "亜急性硬化性全脳炎",
    "mondo_label_en": "subacute sclerosing panencephalitis",
    "mondo_url": "https://monarchinitiative.org/MONDO:0009835"
  },
  {
    "nando_id": "NANDO:1200198",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200198",
    "nando_label_ja": "亜急性進行型硬化性全脳炎",
    "nando_label_en": "Subacute progressive sclerosing panencephalitis",
    "mondo_id": "MONDO:0009835",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_label_ja": "亜急性硬化性全脳炎",
    "mondo_label_en": "subacute sclerosing panencephalitis",
    "mondo_url": "https://monarchinitiative.org/MONDO:0009835"
  },
  {
    "nando_id": "NANDO:1200785",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200785",
    "nando_label_ja": "フェニルアラニン水酸化酵素欠損症",
    "nando_label_en": "Phenylalanine hydroxylase deficiency",
    "mondo_id": "MONDO:0009861",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_label_ja": "フェニルケトン尿症",
    "mondo_label_en": "phenylketonuria",
    "mondo_url": "https://monarchinitiative.org/MONDO:0009861"
  },
  {
    "nando_id": "NANDO:1200423",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200423",
    "nando_label_ja": "呼吸細気管支炎関連間質性肺炎",
    "nando_label_en": "Respiratory bronchiolitis-associated interstitial lung disease",
    "mondo_id": "MONDO:0009887",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_label_ja": "剥離性間質性肺炎",
    "mondo_label_en": "desquamative interstitial pneumonia",
    "mondo_url": "https://monarchinitiative.org/MONDO:0009887"
  },
  {
    "nando_id": "NANDO:1200280",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200280",
    "nando_label_ja": "一次性シェーグレン症候群",
    "nando_label_en": "Primary Sjogren's syndrome",
    "mondo_id": "MONDO:0010030",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_label_ja": "シェーグレン症候群",
    "mondo_label_en": "Sjogren syndrome",
    "mondo_url": "https://monarchinitiative.org/MONDO:0010030"
  },
  {
    "nando_id": "NANDO:1200084",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200084",
    "nando_label_ja": "新生児型マルチプルスルファターゼ欠損症",
    "nando_label_en": "Neonatal multiple sulfatase deficiency",
    "mondo_id": "MONDO:0010088",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_label_ja": "マルチプルサルファターゼ欠損症",
    "mondo_label_en": "mucosulfatidosis",
    "mondo_url": "https://monarchinitiative.org/MONDO:0010088"
  },
  {
    "nando_id": "NANDO:1200085",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200085",
    "nando_label_ja": "乳幼児型マルチプルスルファターゼ欠損症",
    "nando_label_en": "Late-infantile multiple sulfatase deficiency",
    "mondo_id": "MONDO:0010088",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_label_ja": "マルチプルサルファターゼ欠損症",
    "mondo_label_en": "mucosulfatidosis",
    "mondo_url": "https://monarchinitiative.org/MONDO:0010088"
  },
  {
    "nando_id": "NANDO:1200395",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200395",
    "nando_label_ja": "甲状腺ホルモン不応症",
    "nando_label_en": "Resistance to thyroid hormone",
    "mondo_id": "MONDO:0010131",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_label_ja": "甲状腺ホルモン不応症, 全身型, 常染色体潜性",
    "mondo_label_en": "thyroid hormone resistance, generalized, autosomal recessive",
    "mondo_url": "https://monarchinitiative.org/MONDO:0010131"
  },
  {
    "nando_id": "NANDO:1200623",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200623",
    "nando_label_ja": "中性脂肪蓄積症",
    "nando_label_en": "Neutral lipid storage disease with ichthyosis",
    "mondo_id": "MONDO:0010155",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_label_ja": "ドルフマン・シャナリン症候群",
    "mondo_label_en": "Dorfman-Chanarin disease",
    "mondo_url": "https://monarchinitiative.org/MONDO:0010155"
  },
  {
    "nando_id": "NANDO:1200403",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200403",
    "nando_label_ja": "先天性副腎低形成症",
    "nando_label_en": "Congenital adrenal hypoplasia",
    "mondo_id": "MONDO:0010264",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_label_ja": "X連鎖性先天性副腎低形成症",
    "mondo_label_en": "X-linked adrenal hypoplasia congenita",
    "mondo_url": "https://monarchinitiative.org/MONDO:0010264"
  },
  {
    "nando_id": "NANDO:1200690",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200690",
    "nando_label_ja": "脆弱Ｘ症候群関連疾患",
    "nando_label_en": "Fragile X syndrome related diseases",
    "mondo_id": "MONDO:0010382",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_label_ja": "脆弱X関連振戦運動失調症候群",
    "mondo_label_en": "fragile X-associated tremor/ataxia syndrome",
    "mondo_url": "https://monarchinitiative.org/MONDO:0010382"
  },
  {
    "nando_id": "NANDO:1200779",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200779",
    "nando_label_ja": "ビタミンD抵抗性くる病",
    "nando_label_en": "Vitamin D-resistant rickets",
    "mondo_id": "MONDO:0010619",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_label_ja": "X連鎖顕性低リン血症性くる病",
    "mondo_label_en": "X-linked dominant hypophosphatemic rickets",
    "mondo_url": "https://monarchinitiative.org/MONDO:0010619"
  },
  {
    "nando_id": "NANDO:1200604",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200604",
    "nando_label_ja": "典型的レット症候群",
    "nando_label_en": "Typical Rett syndrome",
    "mondo_id": "MONDO:0010726",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_label_ja": "レット症候群",
    "mondo_label_en": "Rett syndrome",
    "mondo_url": "https://monarchinitiative.org/MONDO:0010726"
  },
  {
    "nando_id": "NANDO:1200779",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200779",
    "nando_label_ja": "ビタミンD抵抗性くる病",
    "nando_label_en": "Vitamin D-resistant rickets",
    "mondo_id": "MONDO:0010931",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_label_ja": "ビタミンD依存性くる病, 2B型",
    "mondo_label_en": "vitamin D-dependent rickets, type 2B",
    "mondo_url": "https://monarchinitiative.org/MONDO:0010931"
  },
  {
    "nando_id": "NANDO:1200540",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200540",
    "nando_label_ja": "脳内鉄沈着神経変性症4型",
    "nando_label_en": "Neurodegeneration with brain iron accumulation type 4",
    "mondo_id": "MONDO:0011426",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_label_ja": "NBIA４",
    "mondo_label_en": "aceruloplasminemia",
    "mondo_url": "https://monarchinitiative.org/MONDO:0011426"
  },
  {
    "nando_id": "NANDO:1200799",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200799",
    "nando_label_ja": "グルコーストランスポーター1欠損症",
    "nando_label_en": "Glucose transporter 1 deficiency",
    "mondo_id": "MONDO:0011724",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_label_ja": "GLUT1欠損による脳症",
    "mondo_label_en": "encephalopathy due to GLUT1 deficiency",
    "mondo_url": "https://monarchinitiative.org/MONDO:0011724"
  },
  {
    "nando_id": "NANDO:1200748",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200748",
    "nando_label_ja": "特発性肺胞蛋白症",
    "nando_label_en": "Idiopathic pulmonary alveolar proteinosis",
    "mondo_id": "MONDO:0012579",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_label_ja": "自己免疫性肺胞蛋白症",
    "mondo_label_en": "autoimmune pulmonary alveolar proteinosis",
    "mondo_url": "https://monarchinitiative.org/MONDO:0012579"
  },
  {
    "nando_id": "NANDO:1200746",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200746",
    "nando_label_ja": "肺胞蛋白症",
    "nando_label_en": "Pulmonary alveolar proteinosis",
    "mondo_id": "MONDO:0012580",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_label_ja": "遺伝性肺胞蛋白症",
    "mondo_label_en": "hereditary pulmonary alveolar proteinosis",
    "mondo_url": "https://monarchinitiative.org/MONDO:0012580"
  },
  {
    "nando_id": "NANDO:1200541",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200541",
    "nando_label_ja": "FAHN",
    "nando_label_en": "Fatty acid hydroxylase-associated neurodegeneration",
    "mondo_id": "MONDO:0012866",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_label_ja": "遺伝性痙性対麻痺35",
    "mondo_label_en": "hereditary spastic paraplegia 35",
    "mondo_url": "https://monarchinitiative.org/MONDO:0012866"
  },
  {
    "nando_id": "NANDO:1200301",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200301",
    "nando_label_ja": "MDSとの境界型",
    "nando_label_en": "Borderline between aplastic anemia and MDS",
    "mondo_id": "MONDO:0013851",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_label_ja": "常染色体顕性形成不全および骨髄異形成",
    "mondo_label_en": "autosomal dominant aplasia and myelodysplasia",
    "mondo_url": "https://monarchinitiative.org/MONDO:0013851"
  },
  {
    "nando_id": "NANDO:1200218",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200218",
    "nando_label_ja": "縁取り空胞を伴う遠位型ミオパチー",
    "nando_label_en": "Distal myopathy with rimmed vacuoles",
    "mondo_id": "MONDO:0014945",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_label_ja": "ミオパチー, 遠位型, 縁取り空胞を伴う",
    "mondo_label_en": "myopathy, distal, with rimmed vacuoles",
    "mondo_url": "https://monarchinitiative.org/MONDO:0014945"
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  {
    "nando_id": "NANDO:1200622",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200622",
    "nando_label_ja": "ドルフマン・シャナリン症候群",
    "nando_label_en": "Dorfman-Chanarin syndrome",
    "mondo_id": "MONDO:0015611",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_label_ja": "中性脂肪蓄積症",
    "mondo_label_en": "neutral lipid storage disease",
    "mondo_url": "https://monarchinitiative.org/MONDO:0015611"
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    "nando_id": "NANDO:1200301",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200301",
    "nando_label_ja": "MDSとの境界型",
    "nando_label_en": "Borderline between aplastic anemia and MDS",
    "mondo_id": "MONDO:0015909",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_label_ja": "再生不良性貧血",
    "mondo_label_en": "aplastic anemia",
    "mondo_url": "https://monarchinitiative.org/MONDO:0015909"
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  {
    "nando_id": "NANDO:1200649",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200649",
    "nando_label_ja": "後側彎型エーラス・ダンロス症候群",
    "nando_label_en": "Ehlers-Danlos syndrome, kyphoscoliotic type",
    "mondo_id": "MONDO:0016002",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_label_ja": "エーラス・ダンロス症候群, 後側弯型1",
    "mondo_label_en": "Ehlers-Danlos syndrome, kyphoscoliotic type 1",
    "mondo_url": "https://monarchinitiative.org/MONDO:0016002"
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  {
    "nando_id": "NANDO:1200001",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200001",
    "nando_label_ja": "球脊髄性筋萎縮症",
    "nando_label_en": "Spinal and bulbar muscular atrophy",
    "mondo_id": "MONDO:0016113",
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    "mondo_label_ja": "球脊髄性筋萎縮症",
    "mondo_label_en": "bulbospinal muscular atrophy",
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    "nando_id": "NANDO:1200474",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200474",
    "nando_label_ja": "先天性非典型溶血性尿毒症症候群",
    "nando_label_en": "Congenital atypical hemolytic uremic syndrome",
    "mondo_id": "MONDO:0016244",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_label_ja": "非典型溶血性尿毒症症候群",
    "mondo_label_en": "atypical hemolytic-uremic syndrome",
    "mondo_url": "https://monarchinitiative.org/MONDO:0016244"
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    "nando_id": "NANDO:1200442",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200442",
    "nando_label_ja": "自己免疫性肝炎（典型例）",
    "nando_label_en": "Typical autoimmune hepatitis",
    "mondo_id": "MONDO:0016264",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_label_ja": "自己免疫性肝炎",
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    "nando_id": "NANDO:1200701",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200701",
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    "mondo_id": "MONDO:0016301",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_label_ja": "修正大血管転位症",
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    "nando_id": "NANDO:1200701",
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    "mondo_label_ja": "心奇形を伴う完全大血管転位症",
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    "nando_id": "NANDO:1200509",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200509",
    "nando_label_ja": "脊髄髄膜瘤",
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    "mondo_id": "MONDO:0017069",
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    "mondo_label_ja": "脊髄髄膜瘤",
    "mondo_label_en": "spina bifida cystica",
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    "nando_id": "NANDO:1200723",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200723",
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    "mondo_id": "MONDO:0017236",
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    "mondo_label_ja": "急速進行性糸球体腎炎",
    "mondo_label_en": "rapidly progressive glomerulonephritis",
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    "nando_id": "NANDO:1200507",
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    "nando_label_ja": "症候性脊髄空洞症",
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    "mondo_label_ja": "脊髄空洞症",
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    "nando_id": "NANDO:1200539",
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    "mondo_id": "MONDO:0018307",
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    "nando_id": "NANDO:1200542",
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    "mondo_id": "MONDO:0018307",
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    "nando_id": "NANDO:1200162",
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    "mondo_label_ja": "乳児腎性シスチン症",
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    "nando_id": "NANDO:1200396",
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    "mondo_label_ja": "先天性副腎皮質酵素欠損症",
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    "nando_id": "NANDO:1200428",
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    "mondo_label_ja": "肺静脈閉塞症/肺毛細血管腫症",
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    "nando_id": "NANDO:1200440",
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    "mondo_id": "MONDO:0018646",
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    "mondo_label_ja": "硬化性胆管炎",
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    "nando_id": "NANDO:1200675",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200675",
    "nando_label_ja": "鰓耳腎症候群",
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    "mondo_id": "MONDO:0018878",
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    "mondo_label_ja": "鰓耳症候群",
    "mondo_label_en": "branchiootic syndrome",
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    "nando_id": "NANDO:1200641",
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    "mondo_label_ja": "眼皮膚白皮症",
    "mondo_label_en": "oculocutaneous albinism",
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    "nando_id": "NANDO:1200339",
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    "nando_label_en": "Thymus hypoplasia",
    "mondo_id": "MONDO:0018923",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_label_ja": "22q11.2欠失症候群",
    "mondo_label_en": "22q11.2 deletion syndrome",
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    "nando_id": "NANDO:1200481",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200481",
    "nando_label_ja": "ミオチュブラーミオパチー",
    "nando_label_en": "Myotubular myopathy",
    "mondo_id": "MONDO:0018947",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_label_ja": "中心核ミオパチー",
    "mondo_label_en": "centronuclear myopathy",
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    "nando_id": "NANDO:1200225",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200225",
    "nando_label_ja": "神経線維腫症",
    "nando_label_en": "Neurofibromatosis",
    "mondo_id": "MONDO:0018975",
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    "mondo_label_ja": "神経線維腫症1型",
    "mondo_label_en": "neurofibromatosis type 1",
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    "nando_id": "NANDO:1200632",
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    "nando_label_ja": "類天疱瘡",
    "nando_label_en": "Pemphigoid (including Epidermolysis bullosa acquisita)",
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    "mondo_label_ja": "類天疱瘡",
    "mondo_label_en": "bullous pemphigoid",
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    "nando_id": "NANDO:1200142",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200142",
    "nando_label_ja": "酸性リパーゼ欠損症",
    "nando_label_en": "Acid lipase deficiency",
    "mondo_id": "MONDO:0019148",
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    "mondo_label_ja": "酸性リパーゼ欠損症",
    "mondo_label_en": "Wolman disease",
    "mondo_url": "https://monarchinitiative.org/MONDO:0019148"
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    "nando_id": "NANDO:1200617",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200617",
    "nando_label_ja": "葉状魚鱗癬",
    "nando_label_en": "Lamellar ichthyosis",
    "mondo_id": "MONDO:0019306",
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    "mondo_label_ja": "先天性魚鱗癬様紅皮症",
    "mondo_label_en": "congenital non-bullous ichthyosiform erythroderma",
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    "nando_id": "NANDO:1200319",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200319",
    "nando_label_ja": "後天性二次性血栓性血小板減少性紫斑病",
    "nando_label_en": "Secondary thrombotic thrombocytopenic purpura",
    "mondo_id": "MONDO:0019740",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_label_ja": "後天性血栓性血小板減少性紫斑病",
    "mondo_label_en": "acquired thrombotic thrombocytopenic purpura",
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  {
    "nando_id": "NANDO:1200219",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200219",
    "nando_label_ja": "眼咽頭遠位型ミオパチー",
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    "mondo_id": "MONDO:0020793",
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    "mondo_label_ja": "眼咽頭遠位型ミオパチー1",
    "mondo_label_en": "oculopharyngodistal myopathy 1",
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    "nando_id": "NANDO:1200226",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200226",
    "nando_label_ja": "神経線維腫症I型",
    "nando_label_en": "Neurofibromatosis type 1",
    "mondo_id": "MONDO:0021061",
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    "mondo_label_ja": "神経線維腫症",
    "mondo_label_en": "neurofibromatosis",
    "mondo_url": "https://monarchinitiative.org/MONDO:0021061"
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    "nando_id": "NANDO:1200227",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200227",
    "nando_label_ja": "神経線維腫症II型",
    "nando_label_en": "Neurofibromatosis type 2",
    "mondo_id": "MONDO:0021061",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_label_ja": "神経線維腫症",
    "mondo_label_en": "neurofibromatosis",
    "mondo_url": "https://monarchinitiative.org/MONDO:0021061"
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    "nando_id": "NANDO:1200127",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200127",
    "nando_label_ja": "乳児型α - マンノシドーシス",
    "nando_label_en": "Alpha-mannosidosis, infantile form",
    "mondo_id": "MONDO:0022424",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_label_ja": "α-マンノシドーシス1型",
    "mondo_label_en": "alpha-mannosidosis type 1",
    "mondo_url": "https://monarchinitiative.org/MONDO:0022424"
  },
  {
    "nando_id": "NANDO:1200778",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200778",
    "nando_label_ja": "ビタミンD抵抗性くる病/骨軟化症",
    "nando_label_en": "Vitamin D-resistant rickets/Vitamin D-resistant osteomalacia",
    "mondo_id": "MONDO:0024300",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_label_ja": "低リン血症性くる病",
    "mondo_label_en": "hypophosphatemic rickets",
    "mondo_url": "https://monarchinitiative.org/MONDO:0024300"
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  {
    "nando_id": "NANDO:1200780",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200780",
    "nando_label_ja": "ビタミンD抵抗性骨軟化症",
    "nando_label_en": "Vitamin D-resistant osteomalacia",
    "mondo_id": "MONDO:0024300",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_label_ja": "低リン血症性くる病",
    "mondo_label_en": "hypophosphatemic rickets",
    "mondo_url": "https://monarchinitiative.org/MONDO:0024300"
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  {
    "nando_id": "NANDO:1200595",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200595",
    "nando_label_ja": "遊走性焦点発作を伴う乳児てんかん",
    "nando_label_en": "Epilepsy of infancy with migrating focal seizures",
    "mondo_id": "MONDO:0100025",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_label_ja": "遊走性焦点発作を伴う乳児てんかん",
    "mondo_label_en": "epilepsy of infancy with migrating focal seizures",
    "mondo_url": "https://monarchinitiative.org/MONDO:0100025"
  },
  {
    "nando_id": "NANDO:1200180",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200180",
    "nando_label_ja": "複合体I欠損症",
    "nando_label_en": "Mitochondrial complex I deficiency",
    "mondo_id": "MONDO:0100224",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_label_ja": "ミトコンドリア複合体I欠損症, 核型1",
    "mondo_label_en": "mitochondrial complex I deficiency, nuclear type 1",
    "mondo_url": "https://monarchinitiative.org/MONDO:0100224"
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  {
    "nando_id": "NANDO:2200008",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_2200008",
    "nando_label_ja": "急性骨髄単球性白血病",
    "nando_label_en": "Acute monocytic leukemia",
    "mondo_id": "MONDO:0000875",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_label_ja": "成人急性単球性白血病",
    "mondo_label_en": "adult acute monocytic leukemia",
    "mondo_url": "https://monarchinitiative.org/MONDO:0000875"
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    "nando_id": "NANDO:2200009",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_2200009",
    "nando_label_ja": "急性単球性白血病",
    "nando_label_en": "Acute monocytic leukemia",
    "mondo_id": "MONDO:0000875",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_label_ja": "成人急性単球性白血病",
    "mondo_label_en": "adult acute monocytic leukemia",
    "mondo_url": "https://monarchinitiative.org/MONDO:0000875"
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    "nando_id": "NANDO:2200141",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_2200141",
    "nando_label_ja": "腎血管性高血圧",
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    "mondo_id": "MONDO:0001105",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_label_ja": "腎性高血圧",
    "mondo_label_en": "renal hypertension",
    "mondo_url": "https://monarchinitiative.org/MONDO:0001105"
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    "nando_id": "NANDO:1200838",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200838",
    "nando_label_ja": "肝型糖原病",
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    "mondo_id": "MONDO:0002412",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_label_ja": "糖原質代謝障害",
    "mondo_label_en": "disorder of glycogen metabolism",
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    "nando_id": "NANDO:1200840",
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    "nando_label_ja": "肝型糖原病Ia型",
    "nando_label_en": "Hepatic glycogen storage disease type Ia",
    "mondo_id": "MONDO:0002413",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_label_ja": "糖原病I",
    "mondo_label_en": "glycogen storage disease I",
    "mondo_url": "https://monarchinitiative.org/MONDO:0002413"
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    "nando_id": "NANDO:2200089",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_2200089",
    "nando_label_ja": "乏突起神経膠腫",
    "nando_label_en": "Oligodendroglioma",
    "mondo_id": "MONDO:0002540",
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    "mondo_label_ja": "小児乏突起膠腫",
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    "nando_id": "NANDO:2200089",
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    "mondo_id": "MONDO:0002543",
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    "mondo_label_ja": "成人乏突起膠腫",
    "mondo_label_en": "adult oligodendroglioma",
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    "mondo_label_ja": "小児骨肉腫",
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    "nando_id": "NANDO:2200090",
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    "mondo_label_ja": "リンパ管腫症/ゴーハム病",
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    "mondo_label_ja": "成人脂肪肉腫",
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    "mondo_label_ja": "小児リンパ腫",
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    "mondo_label_ja": "成人リンパ腫",
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    "mondo_label_ja": "小児卵巣卵黄嚢腫",
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    "nando_id": "NANDO:2100204",
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    "mondo_label_ja": "骨化性筋炎",
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    "mondo_label_ja": "小児若年性毛様細胞性星細胞腫",
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    "mondo_id": "MONDO:0004069",
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    "mondo_label_ja": "先天性ミトコンドリア代謝障害",
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    "nando_label_en": "Leukemia",
    "mondo_id": "MONDO:0004355",
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    "mondo_label_ja": "小児白血病",
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    "mondo_label_ja": "部分中心性脈絡膜萎縮症",
    "mondo_label_en": "partial central choroid dystrophy",
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    "nando_id": "NANDO:2200049",
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    "nando_label_en": "Osteochondromatosis",
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    "nando_id": "NANDO:2200123",
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    "mondo_id": "MONDO:0018904",
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    "mondo_label_ja": "一次性膜性増殖性糸球体腎炎",
    "mondo_label_en": "primary membranoproliferative glomerulonephritis",
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    "mondo_id": "MONDO:0019005",
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    "mondo_label_ja": "ネフロン癆",
    "mondo_label_en": "nephronophthisis",
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    "nando_id": "NANDO:2200138",
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    "mondo_label_ja": "アミロイドーシス",
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    "nando_id": "NANDO:1200815",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200815",
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    "nando_id": "NANDO:1200881",
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    "mondo_id": "MONDO:0019460",
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    "mondo_label_ja": "急性未分化型白血病",
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    "nando_label_ja": "混合型急性白血病",
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    "mondo_id": "MONDO:0019460",
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    "mondo_label_ja": "急性未分化型白血病",
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    "nando_id": "NANDO:1201011",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1201011",
    "nando_label_ja": "限局皮膚硬化型全身性強皮症",
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    "mondo_id": "MONDO:0019563",
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    "mondo_label_ja": "限局皮膚硬化型全身性強皮症",
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    "nando_id": "NANDO:1200962",
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    "mondo_label_ja": "先天性三尖弁狭窄症",
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    "nando_id": "NANDO:2200022",
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    "mondo_label_ja": "前駆B細胞性急性リンパ芽球性白血病",
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    "nando_id": "NANDO:2200087",
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    "nando_label_ja": "膠芽腫",
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    "mondo_id": "MONDO:0020690",
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    "mondo_label_ja": "膠芽腫",
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    "nando_id": "NANDO:1201068",
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    "mondo_id": "MONDO:0022402",
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    "nando_id": "NANDO:1201069",
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    "nando_id": "NANDO:1200841",
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    "mondo_id": "MONDO:0023258",
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    "nando_id": "NANDO:1201090",
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    "mondo_label_ja": "ムコ多糖症1型",
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    "mondo_label_ja": "プロトポルフィリン症, 骨髄性, 1",
    "mondo_label_en": "protoporphyria, erythropoietic, 1",
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    "nando_id": "NANDO:2200712",
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    "nando_label_en": "Thymus hypoplasia",
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    "mondo_label_ja": "ディジョージ症候群",
    "mondo_label_en": "DiGeorge syndrome",
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    "nando_id": "NANDO:2200712",
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    "nando_label_en": "Thymus hypoplasia",
    "mondo_id": "MONDO:0008644",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_label_ja": "口蓋帆・心臓・顔症候群",
    "mondo_label_en": "velocardiofacial syndrome",
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    "nando_id": "NANDO:2201345",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_2201345",
    "nando_label_ja": "軟骨無発生症2型",
    "nando_label_en": "Achondrogenesis type 2",
    "mondo_id": "MONDO:0008703",
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    "mondo_label_ja": "遠位中間肢異形成症2A",
    "mondo_label_en": "acromesomelic dysplasia 2A",
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    "nando_id": "NANDO:2201139",
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    "mondo_id": "MONDO:0008723",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_label_ja": "極長鎖アシルCoA脱水素酵素欠損症",
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    "nando_id": "NANDO:2200948",
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    "mondo_id": "MONDO:0008738",
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    "mondo_label_ja": "神経節細胞欠損症, 全腸管",
    "mondo_label_en": "aganglionosis, total intestinal",
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    "nando_id": "NANDO:2201242",
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    "nando_label_en": "Late infantile neuronal ceroid lipofuscinosis",
    "mondo_id": "MONDO:0008769",
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    "mondo_label_ja": "神経セロイドリポフスチン症2",
    "mondo_label_en": "neuronal ceroid lipofuscinosis 2",
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    "nando_id": "NANDO:2201084",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_2201084",
    "nando_label_ja": "発症前型N-アセチルグルタミン酸合成酵素欠損症",
    "nando_label_en": "Presymptomatic N-acetylglutamate synthetase deficiency",
    "mondo_id": "MONDO:0009377",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_label_ja": "Nアセチルグルタミン酸合成酵素欠損による高アンモニア血症",
    "mondo_label_en": "hyperammonemia due to N-acetylglutamate synthase deficiency",
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    "nando_id": "NANDO:2200346",
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    "nando_label_ja": "自己免疫性多内分泌腺症候群1型",
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    "mondo_id": "MONDO:0009411",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_label_ja": "自己免疫性多内分泌腺症候群1型",
    "mondo_label_en": "autoimmune polyendocrine syndrome type 1",
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    "nando_id": "NANDO:2200738",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_2200738",
    "nando_label_ja": "自己免疫性多腺性内分泌不全症",
    "nando_label_en": "Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy",
    "mondo_id": "MONDO:0009411",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_label_ja": "自己免疫性多内分泌腺症候群1型",
    "mondo_label_en": "autoimmune polyendocrine syndrome type 1",
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    "nando_id": "NANDO:2200537",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_2200537",
    "nando_label_ja": "グリコーゲン合成酵素欠損症",
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    "mondo_id": "MONDO:0009414",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_label_ja": "肝グリコーゲン合成酵素欠損による糖原病",
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    "mondo_url": "https://monarchinitiative.org/MONDO:0009414"
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    "nando_id": "NANDO:2201119",
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    "nando_label_ja": "発症前型3-ヒドロキシ-3-メチルグルタル酸血症",
    "nando_label_en": "Presymptomatic 3-hydroxy-3-methylglutaric acidemia",
    "mondo_id": "MONDO:0009520",
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    "mondo_label_ja": "3-ヒドロキシ-3-メチルグルタル酸尿症",
    "mondo_label_en": "3-hydroxy-3-methylglutaric aciduria",
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    "nando_id": "NANDO:2201193",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_2201193",
    "nando_label_ja": "新生児及び早期乳児型ガラクトシアリドーシス",
    "nando_label_en": "Galactosialidosis, early infantile form",
    "mondo_id": "MONDO:0009738",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_label_ja": "シアリドーシス2型",
    "mondo_label_en": "sialidosis type 2",
    "mondo_url": "https://monarchinitiative.org/MONDO:0009738"
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    "nando_id": "NANDO:2201241",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_2201241",
    "nando_label_ja": "乳児型神経セロイドリポフスチン症",
    "nando_label_en": "Infantile neuronal ceroid lipofuscinosis",
    "mondo_id": "MONDO:0009744",
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    "mondo_label_ja": "神経セロイドリポフスチン症1",
    "mondo_label_en": "neuronal ceroid lipofuscinosis 1",
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    "nando_id": "NANDO:2200950",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_2200950",
    "nando_label_ja": "総排泄腔遺残",
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    "mondo_id": "MONDO:0009774",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_label_ja": "総排泄腔外反症",
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    "nando_id": "NANDO:2200484",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_2200484",
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    "mondo_id": "MONDO:0009796",
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    "nando_id": "NANDO:2200486",
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    "mondo_id": "MONDO:0009796",
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    "nando_id": "NANDO:2200436",
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    "nando_label_ja": "高IgD症候群",
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    "mondo_id": "MONDO:0009849",
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    "mondo_label_ja": "周期熱を伴う高ガンマグロブリン血症D",
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    "nando_id": "NANDO:2201075",
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    "nando_label_ja": "フェニルアラニン水酸化酵素欠損症",
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    "mondo_id": "MONDO:0009861",
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    "mondo_label_ja": "フェニルケトン尿症",
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    "nando_id": "NANDO:2201227",
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    "mondo_label_ja": "マルチプルサルファターゼ欠損症",
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    "nando_id": "NANDO:2201228",
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    "mondo_id": "MONDO:0010298",
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    "mondo_label_ja": "レッシュ・ナイハン症候群",
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    "nando_id": "NANDO:2201147",
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    "nando_id": "NANDO:2200801",
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    "mondo_id": "MONDO:0012584",
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    "mondo_label_ja": "全身性エリテマトーデス, 感受性, 9",
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    "mondo_label_ja": "アデノシンデアミナーゼ2欠損症",
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    "nando_id": "NANDO:2200359",
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    "nando_id": "NANDO:2200284",
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    "nando_id": "NANDO:2201133",
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    "nando_id": "NANDO:2201134",
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    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200023",
    "nando_label_ja": "多発性硬化症",
    "nando_label_en": "Multiple sclerosis",
    "mondo_id": "MONDO:0005301",
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    "mondo_label_ja": "多発性硬化症",
    "mondo_label_en": "multiple sclerosis",
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    "nando_id": "NANDO:1200024",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200024",
    "nando_label_ja": "再発寛解型多発性硬化症",
    "nando_label_en": "Relapsing-remitting multiple sclerosis",
    "mondo_id": "MONDO:0005314",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "再発寛解型多発性硬化症",
    "mondo_label_en": "relapsing-remitting multiple sclerosis",
    "mondo_url": "https://monarchinitiative.org/MONDO:0005314"
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  {
    "nando_id": "NANDO:1200186",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200186",
    "nando_label_ja": "プリオン病",
    "nando_label_en": "Prion disease",
    "mondo_id": "MONDO:0005429",
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    "mondo_label_ja": "プリオン病",
    "mondo_label_en": "prion disease",
    "mondo_url": "https://monarchinitiative.org/MONDO:0005429"
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  {
    "nando_id": "NANDO:1100006",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1100006",
    "nando_label_ja": "血液系疾患",
    "nando_label_en": "Blood disease",
    "mondo_id": "MONDO:0005570",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "血液障害",
    "mondo_label_en": "hematologic disorder",
    "mondo_url": "https://monarchinitiative.org/MONDO:0005570"
  },
  {
    "nando_id": "NANDO:1200278",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200278",
    "nando_label_ja": "混合性結合組織病",
    "nando_label_en": "Mixed connective tissue disease",
    "mondo_id": "MONDO:0005854",
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    "mondo_label_ja": "混合性結合組織病",
    "mondo_label_en": "mixed connective tissue disease",
    "mondo_url": "https://monarchinitiative.org/MONDO:0005854"
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    "nando_id": "NANDO:1200234",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200234",
    "nando_label_ja": "表皮水疱症",
    "nando_label_en": "Epidermolysis bullosa",
    "mondo_id": "MONDO:0006541",
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    "mondo_label_ja": "表皮水疱症",
    "mondo_label_en": "epidermolysis bullosa",
    "mondo_url": "https://monarchinitiative.org/MONDO:0006541"
  },
  {
    "nando_id": "NANDO:1200228",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200228",
    "nando_label_ja": "天疱瘡",
    "nando_label_en": "Pemphigus",
    "mondo_id": "MONDO:0006594",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "天疱瘡",
    "mondo_label_en": "pemphigus",
    "mondo_url": "https://monarchinitiative.org/MONDO:0006594"
  },
  {
    "nando_id": "NANDO:1200030",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200030",
    "nando_label_ja": "慢性炎症性脱髄性多発神経炎",
    "nando_label_en": "Chronic inflammatory demyelinating polyneuropathy",
    "mondo_id": "MONDO:0006702",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "慢性炎症性脱髄性多発神経根ニューロパチー",
    "mondo_label_en": "chronic inflammatory demyelinating polyradiculoneuropathy",
    "mondo_url": "https://monarchinitiative.org/MONDO:0006702"
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  {
    "nando_id": "NANDO:1200194",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200194",
    "nando_label_ja": "変異型クロイツフェルトヤコブ病",
    "nando_label_en": "Variant Creutzfeldt-Jakob disease",
    "mondo_id": "MONDO:0007012",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "変異型クロイツフェルトヤコブ病",
    "mondo_label_en": "variant Creutzfeldt-Jakob disease",
    "mondo_url": "https://monarchinitiative.org/MONDO:0007012"
  },
  {
    "nando_id": "NANDO:1200227",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200227",
    "nando_label_ja": "神経線維腫症II型",
    "nando_label_en": "Neurofibromatosis type 2",
    "mondo_id": "MONDO:0007039",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "NF2関連神経鞘腫症",
    "mondo_label_en": "NF2-related schwannomatosis",
    "mondo_url": "https://monarchinitiative.org/MONDO:0007039"
  },
  {
    "nando_id": "NANDO:1200323",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200323",
    "nando_label_ja": "アデノシンデアミナーゼ欠損症",
    "nando_label_en": "Adenosine deaminase deficiency",
    "mondo_id": "MONDO:0007064",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "重症複合免疫不全症, 常染色体潜性, T細胞陰性, B細胞陰性, NK細胞陰性, アデノシンデアミナーゼ欠損による",
    "mondo_label_en": "severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-negative, due to adenosine deaminase deficiency",
    "mondo_url": "https://monarchinitiative.org/MONDO:0007064"
  },
  {
    "nando_id": "NANDO:1200041",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200041",
    "nando_label_ja": "脊髄小脳失調症3型",
    "nando_label_en": "Spinocerebellar ataxia type 3",
    "mondo_id": "MONDO:0007182",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "マシャド・ジョセフ病",
    "mondo_label_en": "Machado-Joseph disease",
    "mondo_url": "https://monarchinitiative.org/MONDO:0007182"
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  {
    "nando_id": "NANDO:1200284",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200284",
    "nando_label_ja": "ベーチェット病",
    "nando_label_en": "Behcet's disease",
    "mondo_id": "MONDO:0007191",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "ベーチェット病",
    "mondo_label_en": "Behcet disease",
    "mondo_url": "https://monarchinitiative.org/MONDO:0007191"
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  {
    "nando_id": "NANDO:1200044",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200044",
    "nando_label_ja": "脊髄小脳失調症31型",
    "nando_label_en": "Spinocerebellar ataxia type 31",
    "mondo_id": "MONDO:0007296",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "脊髄小脳失調症31型",
    "mondo_label_en": "spinocerebellar ataxia type 31",
    "mondo_url": "https://monarchinitiative.org/MONDO:0007296"
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  {
    "nando_id": "NANDO:1200189",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200189",
    "nando_label_ja": "家族性クロイツフェルト・ヤコブ病",
    "nando_label_en": "Familial Creutzfeldt-Jakob disease",
    "mondo_id": "MONDO:0007403",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "遺伝性クロイツフェルト・ヤコブ病",
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    "nando_id": "NANDO:1200043",
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    "nando_label_ja": "歯状核赤核淡蒼球ルイ体萎縮症",
    "nando_label_en": "Dentatorubropallidoluysian atrophy",
    "mondo_id": "MONDO:0007435",
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    "mondo_label_ja": "歯状核赤核淡蒼球ルイ体萎縮症",
    "mondo_label_en": "dentatorubral-pallidoluysian atrophy",
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    "nando_id": "NANDO:1200190",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200190",
    "nando_label_ja": "ゲルストマン・ストロイスラー・シャインカー病",
    "nando_label_en": "Gerstmann-Straussler-Scheinker syndrome",
    "mondo_id": "MONDO:0007656",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "ゲルストマン・シュトロイスラー・シャインカー症候群",
    "mondo_label_en": "Gerstmann-Straussler-Scheinker syndrome",
    "mondo_url": "https://monarchinitiative.org/MONDO:0007656"
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  {
    "nando_id": "NANDO:1200012",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200012",
    "nando_label_ja": "ハンチントン病",
    "nando_label_en": "Huntington's disease",
    "mondo_id": "MONDO:0007739",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "ハンチントン病",
    "mondo_label_en": "Huntington disease",
    "mondo_url": "https://monarchinitiative.org/MONDO:0007739"
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    "nando_id": "NANDO:1200034",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200034",
    "nando_label_ja": "多系統萎縮症",
    "nando_label_en": "Multiple system atrophy",
    "mondo_id": "MONDO:0007803",
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    "mondo_label_ja": "多系統萎縮症",
    "mondo_label_en": "multiple system atrophy",
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    "nando_id": "NANDO:1200032",
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    "nando_label_ja": "封入体筋炎",
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    "mondo_id": "MONDO:0007827",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "封入体筋炎",
    "mondo_label_en": "inclusion body myositis",
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    "nando_id": "NANDO:1200272",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200272",
    "nando_label_ja": "全身性エリテマトーデス",
    "nando_label_en": "Systemic lupus erythematosus",
    "mondo_id": "MONDO:0007915",
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    "mondo_label_ja": "全身性エリテマトーデス",
    "mondo_label_en": "systemic lupus erythematosus",
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    "nando_id": "NANDO:1200220",
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    "nando_label_ja": "ベスレムミオパチー",
    "nando_label_en": "Bethlem Myopathy",
    "mondo_id": "MONDO:0008029",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "ベスレムミオパチー",
    "mondo_label_en": "Bethlem myopathy",
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    "nando_id": "NANDO:1200206",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200206",
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    "mondo_id": "MONDO:0008039",
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    "mondo_label_ja": "熱帯性痙性不全対麻痺",
    "mondo_label_en": "tropical spastic paraparesis",
    "mondo_url": "https://monarchinitiative.org/MONDO:0008039"
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    "nando_id": "NANDO:1200045",
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    "nando_label_ja": "脊髄小脳失調症1型",
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    "mondo_id": "MONDO:0008119",
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    "mondo_label_ja": "脊髄小脳失調症1型",
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    "nando_id": "NANDO:1200229",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200229",
    "nando_label_ja": "尋常性天疱瘡",
    "nando_label_en": "Pemphigus vulgaris",
    "mondo_id": "MONDO:0008219",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "尋常性天疱瘡",
    "mondo_label_en": "pemphigus vulgaris",
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    "nando_id": "NANDO:1200239",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200239",
    "nando_label_ja": "キンドラー症候群",
    "nando_label_en": "Kindler syndrome",
    "mondo_id": "MONDO:0008260",
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    "mondo_label_ja": "キンドラー症候群",
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    "nando_id": "NANDO:1200042",
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    "mondo_id": "MONDO:0008457",
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    "mondo_label_ja": "脊髄小脳失調症6型",
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    "nando_id": "NANDO:1200046",
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    "nando_label_ja": "脊髄小脳失調症2型",
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    "mondo_id": "MONDO:0008458",
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    "mondo_label_ja": "脊髄小脳失調症2型",
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    "nando_id": "NANDO:1200258",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200258",
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    "mondo_id": "MONDO:0008538",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "側頭動脈炎",
    "mondo_label_en": "temporal arteritis",
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    "nando_id": "NANDO:1200315",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200315",
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    "mondo_id": "MONDO:0008558",
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    "mondo_label_ja": "自己免疫性血小板減少性紫斑病",
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    "nando_id": "NANDO:1200014",
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    "mondo_id": "MONDO:0008695",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "VPS13A関連神経変性疾患",
    "mondo_label_en": "VPS13A-related neurodegenerative disease",
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    "nando_id": "NANDO:1200133",
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    "mondo_id": "MONDO:0008830",
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    "mondo_label_ja": "アスパルチルグルコサミン尿症",
    "mondo_label_en": "aspartylglucosaminuria",
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    "nando_id": "NANDO:1200331",
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    "nando_label_en": "Ataxia telangiectasia",
    "mondo_id": "MONDO:0008840",
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    "mondo_label_ja": "毛細血管拡張性運動失調症",
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    "nando_id": "NANDO:1200051",
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    "mondo_label_ja": "運動失調, 早発性, 眼球運動失行および低アルブミン血症を伴う",
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    "nando_id": "NANDO:1200329",
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    "nando_label_ja": "MHCクラスII欠損症",
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    "mondo_id": "MONDO:0008855",
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    "mondo_label_ja": "MHCクラスII欠損症",
    "mondo_label_en": "MHC class II deficiency",
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    "nando_id": "NANDO:1200266",
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    "nando_label_ja": "バージャー病",
    "nando_label_en": "Buerger's disease",
    "mondo_id": "MONDO:0008889",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "閉塞性血栓血管炎",
    "mondo_label_en": "thromboangiitis obliterans",
    "mondo_url": "https://monarchinitiative.org/MONDO:0008889"
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    "nando_id": "NANDO:1200207",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200207",
    "nando_label_ja": "特発性基底核石灰化症",
    "nando_label_en": "Idiopathic basal ganglia calcification",
    "mondo_id": "MONDO:0008947",
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    "mondo_label_ja": "両側性大脳基底核石灰化症",
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    "mondo_label_ja": "眼型シスチン症",
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    "mondo_label_ja": "劣性栄養障害型表皮水疱症",
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    "mondo_label_ja": "ファーバー脂肪肉芽腫症",
    "mondo_label_en": "Farber lipogranulomatosis",
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    "mondo_label_ja": "GM1ガングリオシドーシス1型",
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    "mondo_id": "MONDO:0009261",
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    "mondo_label_ja": "GM1ガングリオシドーシス2型",
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    "mondo_label_ja": "GM1ガングリオシドーシス3型",
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    "mondo_id": "MONDO:0009265",
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    "mondo_label_ja": "ゴーシェ病I型",
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    "mondo_id": "MONDO:0009266",
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    "mondo_label_ja": "ゴーシェ病II型",
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    "mondo_id": "MONDO:0009267",
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    "mondo_label_ja": "ゴーシェ病III型",
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    "nando_id": "NANDO:1200074",
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    "nando_label_ja": "クラッベ病",
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    "mondo_id": "MONDO:0009499",
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    "mondo_label_ja": "クラッベ病",
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    "mondo_label_ja": "α-マンノシドーシス",
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    "mondo_label_ja": "結節性硬化症",
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    "nando_label_ja": "特発性間質性肺炎",
    "nando_label_en": "Idiopathic interstitial pneumonia",
    "mondo_id": "MONDO:0002429",
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    "mondo_label_ja": "特発性間質性肺炎",
    "mondo_label_en": "idiopathic interstitial pneumonia",
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    "nando_id": "NANDO:1200626",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200626",
    "nando_label_ja": "IBID",
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    "mondo_id": "MONDO:0002470",
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    "mondo_label_ja": "光線過敏性裂毛症",
    "mondo_label_en": "photosensitive trichothiodystrophy",
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    "nando_id": "NANDO:1200364",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200364",
    "nando_label_ja": "先天性補体欠損症",
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    "mondo_id": "MONDO:0003832",
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    "mondo_label_ja": "補体欠損症",
    "mondo_label_en": "complement deficiency",
    "mondo_url": "https://monarchinitiative.org/MONDO:0003832"
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  {
    "nando_id": "NANDO:1200345",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200345",
    "nando_label_ja": "高IgM症候群",
    "nando_label_en": "Hyper-IgM syndrome",
    "mondo_id": "MONDO:0003947",
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    "mondo_label_ja": "高IgM症候群",
    "mondo_label_en": "hyper-IgM syndrome",
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    "nando_id": "NANDO:1200368",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200368",
    "nando_label_ja": "常染色体優性多発性嚢胞腎",
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    "mondo_id": "MONDO:0004691",
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    "mondo_label_ja": "常染色体顕性多発性嚢胞腎",
    "mondo_label_en": "autosomal dominant polycystic kidney disease",
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    "nando_id": "NANDO:1200444",
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    "mondo_id": "MONDO:0005011",
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    "mondo_label_ja": "クローン病",
    "mondo_label_en": "Crohn disease",
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    "nando_id": "NANDO:1200449",
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    "nando_label_ja": "潰瘍性大腸炎",
    "nando_label_en": "Ulcerative colitis",
    "mondo_id": "MONDO:0005101",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "潰瘍性大腸炎",
    "mondo_label_en": "ulcerative colitis",
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    "nando_id": "NANDO:1200387",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200387",
    "nando_label_ja": "下垂体前葉機能低下症",
    "nando_label_en": "Hypopituitarism syndrome",
    "mondo_id": "MONDO:0005152",
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    "mondo_label_ja": "下垂体機能低下症",
    "mondo_label_en": "hypopituitarism",
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    "nando_id": "NANDO:1200366",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200366",
    "nando_label_ja": "IgＡ腎症",
    "nando_label_en": "IgA nephropathy",
    "mondo_id": "MONDO:0005342",
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    "mondo_label_ja": "IgＡ腎症",
    "mondo_label_en": "IgA glomerulonephritis",
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    "nando_id": "NANDO:1200456",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200456",
    "nando_label_ja": "好酸球性食道炎",
    "nando_label_en": "Eosinophilic esophagitis",
    "mondo_id": "MONDO:0005361",
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    "mondo_label_ja": "好酸球性食道炎",
    "mondo_label_en": "eosinophilic esophagitis",
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    "nando_id": "NANDO:1200439",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200439",
    "nando_label_ja": "原発性胆汁性胆管炎",
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    "mondo_id": "MONDO:0005388",
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    "mondo_label_ja": "原発性胆汁性胆管炎",
    "mondo_label_en": "primary biliary cholangitis",
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    "nando_id": "NANDO:1200446",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200446",
    "nando_label_ja": "大腸型クローン病",
    "nando_label_en": "Colonic Crohn's disease",
    "mondo_id": "MONDO:0005532",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "大腸型クローン病",
    "mondo_label_en": "Crohn's colitis",
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    "nando_id": "NANDO:1200451",
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    "mondo_id": "MONDO:0005533",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "潰瘍性大腸炎（左側大腸炎型）",
    "mondo_label_en": "distal colitis",
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    "nando_id": "NANDO:1200447",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200447",
    "nando_label_ja": "小腸大腸型クローン病",
    "nando_label_en": "Crohn ileocolitis",
    "mondo_id": "MONDO:0005534",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "小腸大腸型クローン病",
    "mondo_label_en": "ileocolitis",
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    "nando_id": "NANDO:1200450",
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    "mondo_id": "MONDO:0005536",
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    "mondo_label_ja": "潰瘍性大腸炎（全大腸炎型）",
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    "nando_id": "NANDO:1200445",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200445",
    "nando_label_ja": "小腸型クローン病",
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    "mondo_label_ja": "小腸型クローン病",
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    "nando_id": "NANDO:1200372",
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    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "脊柱管狭窄症",
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    "nando_id": "NANDO:1200376",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200376",
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    "mondo_id": "MONDO:0006802",
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    "mondo_label_ja": "抗利尿ホルモン不適合分泌症候群",
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    "nando_id": "NANDO:1200675",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200675",
    "nando_label_ja": "鰓耳腎症候群",
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    "nando_id": "NANDO:1200667",
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    "nando_label_ja": "アペール症候群",
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    "mondo_id": "MONDO:0007041",
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    "nando_id": "NANDO:1200668",
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    "mondo_label_ja": "ファイファー症候群",
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    "nando_id": "NANDO:1200479",
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    "nando_id": "NANDO:1200666",
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    "mondo_label_ja": "クルーゾン症候群",
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    "mondo_label_ja": "神経下垂体性尿崩症",
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    "nando_id": "NANDO:1200512",
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    "mondo_label_ja": "捻転ジストニア4",
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    "nando_id": "NANDO:1200523",
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    "nando_id": "NANDO:1200472",
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    "mondo_label_ja": "TNF受容体1関連周期性発熱症候群",
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    "nando_id": "NANDO:1200613",
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    "mondo_label_ja": "表在性表皮融解性魚鱗癬",
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    "nando_id": "NANDO:1200644",
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    "mondo_id": "MONDO:0007947",
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    "mondo_label_ja": "マルファン症候群",
    "mondo_label_en": "Marfan syndrome",
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    "nando_id": "NANDO:1200559",
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    "nando_label_ja": "メビウス症候群",
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    "mondo_label_ja": "メビウス症候群",
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    "nando_id": "NANDO:1200354",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200354",
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    "mondo_id": "MONDO:0008090",
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    "mondo_label_ja": "周期性好中球減少症",
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    "nando_id": "NANDO:1200493",
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    "nando_label_en": "Oculopharyngeal muscular dystrophy",
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    "mondo_label_ja": "眼咽頭筋型筋ジストロフィー",
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    "nando_id": "NANDO:1200501",
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    "nando_label_ja": "先天性パラミオトニー",
    "nando_label_en": "Paramyotonia congenita",
    "mondo_id": "MONDO:0008195",
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    "mondo_label_ja": "Von Eulenburg先天性パラミオトニア",
    "mondo_label_en": "paramyotonia congenita of Von Eulenburg",
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  {
    "nando_id": "NANDO:1200547",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200547",
    "nando_label_ja": "ペリー病",
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    "mondo_id": "MONDO:0008201",
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    "mondo_label_ja": "ペリー症候群",
    "mondo_label_en": "Perry syndrome",
    "mondo_url": "https://monarchinitiative.org/MONDO:0008201"
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    "nando_id": "NANDO:1200631",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200631",
    "nando_label_ja": "家族性良性慢性天疱瘡",
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    "mondo_id": "MONDO:0008218",
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    "mondo_label_ja": "ヘイリー・ヘイリー病",
    "mondo_label_en": "Hailey-Hailey disease",
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    "nando_id": "NANDO:1200503",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200503",
    "nando_label_ja": "遺伝性低カリウム性周期性四肢麻痺",
    "nando_label_en": "Hereditary hypokalemic periodic paralysis",
    "mondo_id": "MONDO:0008223",
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    "mondo_label_ja": "低カリウム性周期性四肢麻痺",
    "mondo_label_en": "hypokalemic periodic paralysis",
    "mondo_url": "https://monarchinitiative.org/MONDO:0008223"
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  {
    "nando_id": "NANDO:1200504",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200504",
    "nando_label_ja": "遺伝性高カリウム性周期性四肢麻痺",
    "nando_label_en": "Hereditary hyperkalemic periodic paralysis",
    "mondo_id": "MONDO:0008224",
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    "mondo_label_ja": "高カリウム性周期性四肢麻痺",
    "mondo_label_en": "hyperkalemic periodic paralysis",
    "mondo_url": "https://monarchinitiative.org/MONDO:0008224"
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  {
    "nando_id": "NANDO:1200678",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200678",
    "nando_label_ja": "プラダー・ウィリ症候群",
    "nando_label_en": "Prader-Willi syndrome",
    "mondo_id": "MONDO:0008300",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "プラダー・ウィリ症候群",
    "mondo_label_en": "Prader-Willi syndrome",
    "mondo_url": "https://monarchinitiative.org/MONDO:0008300"
  },
  {
    "nando_id": "NANDO:1200606",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200606",
    "nando_label_ja": "スタージ・ウェーバー症候群",
    "nando_label_en": "Sturge-Weber syndrome",
    "mondo_id": "MONDO:0008501",
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    "mondo_label_ja": "スタージ・ウェーバー症候群",
    "mondo_label_en": "Sturge-Weber syndrome",
    "mondo_url": "https://monarchinitiative.org/MONDO:0008501"
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  {
    "nando_id": "NANDO:1200558",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200558",
    "nando_label_ja": "先天性核上性球麻痺",
    "nando_label_en": "Congenital suprabulbar paresis",
    "mondo_id": "MONDO:0008503",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "先天性核上性球麻痺",
    "mondo_label_en": "Worster-Drought syndrome",
    "mondo_url": "https://monarchinitiative.org/MONDO:0008503"
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  {
    "nando_id": "NANDO:1200476",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200476",
    "nando_label_ja": "ブラウ症候群",
    "nando_label_en": "Blau syndrome",
    "mondo_id": "MONDO:0008523",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "ブラウ症候群",
    "mondo_label_en": "Blau syndrome",
    "mondo_url": "https://monarchinitiative.org/MONDO:0008523"
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  {
    "nando_id": "NANDO:1200467",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200467",
    "nando_label_ja": "マックル・ウェルズ症候群",
    "nando_label_en": "Muckle-Wells syndrome",
    "mondo_id": "MONDO:0008633",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "マックル・ウェルズ症候群",
    "mondo_label_en": "Muckle-Wells syndrome",
    "mondo_url": "https://monarchinitiative.org/MONDO:0008633"
  },
  {
    "nando_id": "NANDO:1200657",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200657",
    "nando_label_ja": "VATER症候群",
    "nando_label_en": "VATER syndrome",
    "mondo_id": "MONDO:0008642",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "VATER/VATER連合",
    "mondo_label_en": "VACTERL/vater association",
    "mondo_url": "https://monarchinitiative.org/MONDO:0008642"
  },
  {
    "nando_id": "NANDO:1200664",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200664",
    "nando_label_ja": "ウィリアムズ症候群",
    "nando_label_en": "Williams syndrome",
    "mondo_id": "MONDO:0008678",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "ウィリアムズ症候群",
    "mondo_label_en": "Williams syndrome",
    "mondo_url": "https://monarchinitiative.org/MONDO:0008678"
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  {
    "nando_id": "NANDO:1200398",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200398",
    "nando_label_ja": "3β−水酸化ステロイド脱水素酵素欠損症",
    "nando_label_en": "3-β-Hydroxysteroid dehydrogenase deficiency",
    "mondo_id": "MONDO:0008727",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "3β-ヒドロキシステロイド脱水素酵素欠損による先天性副腎過形成",
    "mondo_label_en": "congenital adrenal hyperplasia due to 3-beta-hydroxysteroid dehydrogenase deficiency",
    "mondo_url": "https://monarchinitiative.org/MONDO:0008727"
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  {
    "nando_id": "NANDO:1200399",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200399",
    "nando_label_ja": "21-水酸化酵素欠損症",
    "nando_label_en": "21-Hydroxylase deficiency",
    "mondo_id": "MONDO:0008728",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "21水酸化酵素欠損による古典型先天性副腎過形成",
    "mondo_label_en": "classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency",
    "mondo_url": "https://monarchinitiative.org/MONDO:0008728"
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  {
    "nando_id": "NANDO:1200400",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200400",
    "nando_label_ja": "11β-水酸化酵素欠損症",
    "nando_label_en": "11-β-Hydroxylase deficiency",
    "mondo_id": "MONDO:0008729",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "11β-水酸化酵素欠損による先天性副腎過形成",
    "mondo_label_en": "congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency",
    "mondo_url": "https://monarchinitiative.org/MONDO:0008729"
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  {
    "nando_id": "NANDO:1200401",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200401",
    "nando_label_ja": "17α−水酸化酵素欠損症",
    "nando_label_en": "17-α-Hydroxylase deficiency",
    "mondo_id": "MONDO:0008730",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "17α-水酸化酵素欠損による先天性副腎過形成",
    "mondo_label_en": "congenital adrenal hyperplasia due to 17-alpha-hydroxylase deficiency",
    "mondo_url": "https://monarchinitiative.org/MONDO:0008730"
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  {
    "nando_id": "NANDO:1200460",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200460",
    "nando_label_ja": "腸管神経節細胞僅少症",
    "nando_label_en": "Congenital isolated hypoganglionosis",
    "mondo_id": "MONDO:0008738",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "神経節細胞欠損症, 全腸管",
    "mondo_label_en": "aganglionosis, total intestinal",
    "mondo_url": "https://monarchinitiative.org/MONDO:0008738"
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  {
    "nando_id": "NANDO:1200554",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200554",
    "nando_label_ja": "アレキサンダー病",
    "nando_label_en": "Alexander disease",
    "mondo_id": "MONDO:0008752",
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    "mondo_label_ja": "アレキサンダー病",
    "mondo_label_en": "Alexander disease",
    "mondo_url": "https://monarchinitiative.org/MONDO:0008752"
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  {
    "nando_id": "NANDO:1200669",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200669",
    "nando_label_ja": "アントレー・ビクスラー症候群",
    "nando_label_en": "Antley-Bixler syndrome",
    "mondo_id": "MONDO:0008803",
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    "mondo_label_ja": "アントレー・ビクスラー症候群",
    "mondo_label_en": "Antley-Bixler syndrome",
    "mondo_url": "https://monarchinitiative.org/MONDO:0008803"
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    "nando_id": "NANDO:1200333",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200333",
    "nando_label_ja": "ブルーム症候群",
    "nando_label_en": "Bloom syndrome",
    "mondo_id": "MONDO:0008876",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "ブルーム症候群",
    "mondo_label_en": "Bloom syndrome",
    "mondo_url": "https://monarchinitiative.org/MONDO:0008876"
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    "nando_id": "NANDO:1200350",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200350",
    "nando_label_ja": "チェディアック・東症候群",
    "nando_label_en": "Chédiak-Higashi syndrome",
    "mondo_id": "MONDO:0008963",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "チェディアック・東症候群",
    "mondo_label_en": "Chediak-Higashi syndrome",
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    "nando_id": "NANDO:1200464",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200464",
    "nando_label_ja": "チャージ症候群",
    "nando_label_en": "CHARGE syndrome",
    "mondo_id": "MONDO:0008965",
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    "mondo_label_ja": "CHARGE症候群",
    "mondo_label_en": "CHARGE syndrome",
    "mondo_url": "https://monarchinitiative.org/MONDO:0008965"
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    "nando_id": "NANDO:1200463",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200463",
    "nando_label_ja": "コステロ症候群",
    "nando_label_en": "Costello syndrome",
    "mondo_id": "MONDO:0009026",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "コステロ症候群",
    "mondo_label_en": "Costello syndrome",
    "mondo_url": "https://monarchinitiative.org/MONDO:0009026"
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    "nando_id": "NANDO:1200379",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200379",
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    "mondo_id": "MONDO:0009050",
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    "mondo_label_ja": "下垂体腺腫によるクッシング病",
    "mondo_label_en": "Cushing disease due to pituitary adenoma",
    "mondo_url": "https://monarchinitiative.org/MONDO:0009050"
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    "nando_id": "NANDO:1200658",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200658",
    "nando_label_ja": "那須・ハコラ病",
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    "mondo_id": "MONDO:0009092",
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    "mondo_label_ja": "硬化性白質脳症を伴う多囊胞性脂肪膜性骨異形成症",
    "mondo_label_en": "polycystic lipomembranous osteodysplasia with sclerosing leukoencephaly",
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    "nando_id": "NANDO:1200513",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200513",
    "nando_label_ja": "DYT2ジストニア",
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    "mondo_id": "MONDO:0009141",
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    "mondo_label_ja": "捻転ジストニア2",
    "mondo_label_en": "torsion dystonia 2",
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    "nando_id": "NANDO:1200651",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200651",
    "nando_label_ja": "皮膚脆弱型エーラス・ダンロス症候群",
    "nando_label_en": "Ehlers-Danlos syndrome, dermatosparaxis type",
    "mondo_id": "MONDO:0009161",
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    "mondo_label_ja": "エーラス・ダンロス症候群, 皮膚脆弱型",
    "mondo_label_en": "Ehlers-Danlos syndrome, dermatosparaxis type",
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    "nando_id": "NANDO:1200410",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200410",
    "nando_label_ja": "Allgrove症候群",
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    "mondo_id": "MONDO:0009279",
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    "mondo_label_ja": "AAA症候群",
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    "nando_id": "NANDO:1200534",
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    "mondo_id": "MONDO:0009319",
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    "mondo_label_ja": "パントテン酸キナーゼ関連神経変性症",
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    "nando_id": "NANDO:1200341",
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    "mondo_id": "MONDO:0009338",
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    "mondo_label_ja": "肝静脈閉塞症-免疫不全症候群",
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    "nando_id": "NANDO:1200663",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200663",
    "nando_label_ja": "モワット・ウィルソン症候群",
    "nando_label_en": "Mowat-Wilson syndrome",
    "mondo_id": "MONDO:0009341",
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    "mondo_label_ja": "モワット・ウィルソン症候群",
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    "nando_id": "NANDO:1200614",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200614",
    "nando_label_ja": "道化師様魚鱗癬",
    "nando_label_en": "Harlequin ichthyosis",
    "mondo_id": "MONDO:0009443",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "常染色体潜性先天性魚鱗癬4B",
    "mondo_label_en": "autosomal recessive congenital ichthyosis 4B",
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    "nando_id": "NANDO:1200337",
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    "nando_label_ja": "シムケ症候群",
    "nando_label_en": "Schimke syndrome",
    "mondo_id": "MONDO:0009458",
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    "mondo_label_ja": "シムケ免疫・骨異形成症",
    "mondo_label_en": "Schimke immuno-osseous dysplasia",
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    "nando_id": "NANDO:1200662",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200662",
    "nando_label_ja": "有馬症候群",
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    "mondo_id": "MONDO:0009480",
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    "mondo_label_ja": "眼腎障害を伴うジュベール症候群",
    "mondo_label_en": "Joubert syndrome with oculorenal defect",
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    "nando_id": "NANDO:1200602",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200602",
    "nando_label_ja": "ランドウ・クレフナー症候群",
    "nando_label_en": "Landau-Kleffner syndrome",
    "mondo_id": "MONDO:0009509",
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    "mondo_label_ja": "ランドウ・クレフナー症候群",
    "mondo_label_en": "Landau-Kleffner syndrome",
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    "nando_id": "NANDO:1200424",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200424",
    "nando_label_ja": "リンパ球性間質性肺炎",
    "nando_label_en": "Lymphoid interstitial pneumonia",
    "mondo_id": "MONDO:0009537",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "リンパ球性間質性肺炎",
    "mondo_label_en": "lymphoid interstitial pneumonia",
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    "nando_id": "NANDO:1200485",
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    "nando_label_ja": "マリネスコ・シェーグレン症候群",
    "nando_label_en": "Marinesco-Sjogren syndrome",
    "mondo_id": "MONDO:0009567",
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    "mondo_label_ja": "マリネスコ・シェーグレン症候群",
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    "mondo_label_ja": "副甲状腺機能低下症",
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    "mondo_id": "MONDO:0001437",
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    "mondo_label_ja": "肺胞蛋白症",
    "mondo_label_en": "pulmonary alveolar proteinosis",
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    "nando_id": "NANDO:1200723",
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    "mondo_id": "MONDO:0001645",
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    "nando_id": "NANDO:1200815",
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    "nando_label_ja": "赤芽球性プロトポルフィリン症",
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    "mondo_id": "MONDO:0001676",
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    "nando_id": "NANDO:1200793",
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    "mondo_label_ja": "メチルマロン酸血症",
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    "mondo_id": "MONDO:0003136",
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    "mondo_label_ja": "抗基底膜型糸球体腎炎",
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    "mondo_label_ja": "メープルシロップ尿症",
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    "mondo_label_ja": "常染色体潜性家族性地中海熱",
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    "mondo_label_ja": "メチルマロニルCoAムターゼ欠損によるメチルマロン酸尿症",
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    "nando_id": "NANDO:1200822",
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    "nando_id": "NANDO:1200955",
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    "mondo_id": "MONDO:0009697",
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    "mondo_label_ja": "ラフォラ病",
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    "nando_id": "NANDO:1200954",
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    "nando_label_ja": "ウンフェルリヒト・ルントボルグ病",
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    "mondo_id": "MONDO:0009698",
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    "mondo_label_en": "Unverricht-Lundborg syndrome",
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    "nando_id": "NANDO:1201071",
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    "nando_label_ja": "多小脳回",
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    "mondo_id": "MONDO:0000087",
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    "mondo_label_ja": "多小脳回",
    "mondo_label_en": "polymicrogyria",
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    "nando_id": "NANDO:2100135",
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    "nando_label_ja": "思春期早発症",
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    "mondo_id": "MONDO:0000088",
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    "mondo_label_ja": "思春期早発症",
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    "nando_id": "NANDO:2100257",
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    "nando_id": "NANDO:1201032",
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    "mondo_id": "MONDO:0000456",
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    "mondo_label_ja": "脳クレアチン欠乏症候群",
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    "mondo_id": "MONDO:0000521",
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    "mondo_label_ja": "唾液腺癌",
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    "mondo_label_ja": "小児B細胞性急性リンパ芽球性白血病",
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    "nando_id": "NANDO:2100177",
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    "mondo_label_ja": "甲状腺癌",
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    "mondo_label_ja": "組織球症",
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    "mondo_label_ja": "ラブドイド腫瘍",
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    "mondo_label_ja": "心弁膜障害",
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    "mondo_label_ja": "T細胞性急性リンパ芽球性白血病",
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    "mondo_label_ja": "末梢性T細胞リンパ腫, 非特定型",
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    "mondo_label_ja": "副腎褐色細胞腫",
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    "mondo_label_ja": "副腎皮質癌",
    "mondo_label_en": "adrenal cortex carcinoma",
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    "nando_label_ja": "心房中隔欠損症",
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    "mondo_label_ja": "心房中隔欠損",
    "mondo_label_en": "atrial septal defect",
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    "nando_label_ja": "偽性副甲状腺機能低下症Ia型",
    "nando_label_en": "Pseudohypoparathyroidism type 1A",
    "mondo_id": "MONDO:0007078",
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    "mondo_label_en": "pseudohypoparathyroidism type 1A",
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    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1201063",
    "nando_label_ja": "家族性アミロイドニューロパチーIV型",
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    "mondo_id": "MONDO:0007097",
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    "mondo_label_ja": "フィンランド型アミロイドーシス",
    "mondo_label_en": "Finnish type amyloidosis",
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    "nando_id": "NANDO:2200047",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_2200047",
    "nando_label_ja": "肝細胞癌",
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    "mondo_id": "MONDO:0007256",
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    "mondo_label_ja": "肝細胞癌",
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    "nando_id": "NANDO:1201088",
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    "nando_label_ja": "脊椎異形成型エーラス・ダンロス症候群",
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    "mondo_id": "MONDO:0007526",
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    "mondo_label_ja": "エーラス・ダンロス症候群, 脊椎異形成型",
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    "nando_id": "NANDO:1201091",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1201091",
    "nando_label_ja": "歯周型エーラス・ダンロス症候群",
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    "mondo_id": "MONDO:0007527",
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    "mondo_label_ja": "エーラス・ダンロス症候群, 歯周型",
    "mondo_label_en": "Ehlers-Danlos syndrome, periodontitis type",
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    "nando_id": "NANDO:2200009",
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    "nando_label_ja": "急性単球性白血病",
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    "mondo_id": "MONDO:0007896",
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    "mondo_label_ja": "急性単球性白血病",
    "mondo_label_en": "acute monocytic leukemia",
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    "nando_id": "NANDO:1201099",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1201099",
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    "mondo_id": "MONDO:0007986",
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    "mondo_label_ja": "変容性骨異形成症",
    "mondo_label_en": "metatropic dysplasia",
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    "nando_id": "NANDO:1200967",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200967",
    "nando_label_ja": "ネイル・パテラ症候群",
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    "mondo_id": "MONDO:0008061",
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    "mondo_label_ja": "ネイル・パテラ症候群",
    "mondo_label_en": "nail-patella syndrome",
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    "nando_id": "NANDO:1201007",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1201007",
    "nando_label_ja": "ハッチンソン・ギルフォード症候群",
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    "mondo_id": "MONDO:0008310",
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    "mondo_label_ja": "ハッチンソン・ギルフォード早老症候群",
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    "nando_id": "NANDO:2200042",
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    "nando_label_ja": "網膜芽細胞腫",
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    "mondo_id": "MONDO:0008380",
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    "mondo_label_ja": "網膜芽細胞腫",
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    "nando_id": "NANDO:1201100",
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    "nando_label_en": "Spondyloepimetaphyseal dysplasia, Maroteaux type ",
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    "nando_id": "NANDO:1201101",
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    "nando_id": "NANDO:1201078",
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    "mondo_id": "MONDO:0008749",
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    "mondo_label_ja": "偽性副甲状腺機能低下症2型",
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    "nando_id": "NANDO:1200987",
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    "nando_label_ja": "β-ケトチオラーゼ欠損症",
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    "mondo_label_ja": "β-ケトチオラーゼ欠損症",
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    "nando_id": "NANDO:1201006",
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    "nando_id": "NANDO:1200972",
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    "mondo_id": "MONDO:0008919",
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    "mondo_label_ja": "全身性原発性カルニチン欠乏症",
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    "nando_id": "NANDO:2200050",
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    "mondo_label_ja": "軟骨肉腫",
    "mondo_label_en": "chondrosarcoma",
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    "nando_id": "NANDO:1201059",
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    "mondo_label_ja": "バラー・ゲロルト症候群",
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    "nando_id": "NANDO:1201086",
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    "nando_id": "NANDO:1201087",
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    "mondo_label_ja": "脆弱角膜症候群",
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    "mondo_label_ja": "ミラー・ディカー滑脳症候群",
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    "nando_id": "NANDO:1200990",
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    "mondo_label_ja": "先天性筋無力症候群6",
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    "mondo_label_ja": "先天性成長ホルモン単独欠損症",
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    "mondo_id": "MONDO:0000468",
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    "mondo_label_ja": "第3度房室ブロック",
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    "nando_id": "NANDO:2200139",
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    "mondo_id": "MONDO:0000608",
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    "mondo_label_ja": "家族性若年性高尿酸血症性腎症",
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    "nando_label_ja": "未分化神経外胚葉性腫瘍（中枢性のものに限る。）",
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    "nando_id": "NANDO:2200107",
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    "mondo_id": "MONDO:0006711",
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    "mondo_id": "MONDO:0006715",
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    "nando_id": "NANDO:2200234",
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    "mondo_url": "https://monarchinitiative.org/MONDO:0008523"
  },
  {
    "nando_id": "NANDO:2200513",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_2200513",
    "nando_label_ja": "中鎖アシルCoA脱水素酵素欠損症",
    "nando_label_en": "Medium-chain acyl-CoA dehydrogenase deficiency",
    "mondo_id": "MONDO:0008721",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "中鎖アシルCoA脱水素酵素欠損症",
    "mondo_label_en": "medium chain acyl-CoA dehydrogenase deficiency",
    "mondo_url": "https://monarchinitiative.org/MONDO:0008721"
  },
  {
    "nando_id": "NANDO:2200514",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_2200514",
    "nando_label_ja": "短鎖アシルCoA脱水素酵素欠損症",
    "nando_label_en": "Short-chain acyl-CoA dehydrogenase deficiency",
    "mondo_id": "MONDO:0008722",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "短鎖アシルCoA脱水素酵素欠損症",
    "mondo_label_en": "short chain acyl-CoA dehydrogenase deficiency",
    "mondo_url": "https://monarchinitiative.org/MONDO:0008722"
  },
  {
    "nando_id": "NANDO:2200512",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_2200512",
    "nando_label_ja": "極長鎖アシルCoA脱水素酵素欠損症",
    "nando_label_en": "Very-long-chain acyl-CoA dehydrogenase deficiency",
    "mondo_id": "MONDO:0008723",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "極長鎖アシルCoA脱水素酵素欠損症",
    "mondo_label_en": "very long chain acyl-CoA dehydrogenase deficiency",
    "mondo_url": "https://monarchinitiative.org/MONDO:0008723"
  },
  {
    "nando_id": "NANDO:2200371",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_2200371",
    "nando_label_ja": "3β-ヒドロキシステロイド脱水素酵素欠損症",
    "nando_label_en": "3 beta-hydroxysteroid dehydrogenase deficiency",
    "mondo_id": "MONDO:0008727",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "3β-ヒドロキシステロイド脱水素酵素欠損による先天性副腎過形成",
    "mondo_label_en": "congenital adrenal hyperplasia due to 3-beta-hydroxysteroid dehydrogenase deficiency",
    "mondo_url": "https://monarchinitiative.org/MONDO:0008727"
  },
  {
    "nando_id": "NANDO:2200374",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_2200374",
    "nando_label_ja": "21-水酸化酵素欠損症",
    "nando_label_en": "21-Hydroxylase deficiency",
    "mondo_id": "MONDO:0008728",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "21水酸化酵素欠損による古典型先天性副腎過形成",
    "mondo_label_en": "classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency",
    "mondo_url": "https://monarchinitiative.org/MONDO:0008728"
  },
  {
    "nando_id": "NANDO:2200372",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_2200372",
    "nando_label_ja": "11β-水酸化酵素欠損症",
    "nando_label_en": "11-β-Hydroxylase deficiency",
    "mondo_id": "MONDO:0008729",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "11β-水酸化酵素欠損による先天性副腎過形成",
    "mondo_label_en": "congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency",
    "mondo_url": "https://monarchinitiative.org/MONDO:0008729"
  },
  {
    "nando_id": "NANDO:2200373",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_2200373",
    "nando_label_ja": "17α-水酸化酵素欠損症",
    "nando_label_en": "17 alpha-hydroxylase deficiency",
    "mondo_id": "MONDO:0008730",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "17α-水酸化酵素欠損による先天性副腎過形成",
    "mondo_label_en": "congenital adrenal hyperplasia due to 17-alpha-hydroxylase deficiency",
    "mondo_url": "https://monarchinitiative.org/MONDO:0008730"
  },
  {
    "nando_id": "NANDO:2200504",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_2200504",
    "nando_label_ja": "アルカプトン尿症",
    "nando_label_en": "Alkaptonuria",
    "mondo_id": "MONDO:0008753",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "アルカプトン尿症",
    "mondo_label_en": "alkaptonuria",
    "mondo_url": "https://monarchinitiative.org/MONDO:0008753"
  },
  {
    "nando_id": "NANDO:2200493",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_2200493",
    "nando_label_ja": "β-ケトチオラーゼ欠損症",
    "nando_label_en": "Beta-ketothiolase deficiency",
    "mondo_id": "MONDO:0008760",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "β-ケトチオラーゼ欠損症",
    "mondo_label_en": "beta-ketothiolase deficiency",
    "mondo_url": "https://monarchinitiative.org/MONDO:0008760"
  },
  {
    "nando_id": "NANDO:2200482",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_2200482",
    "nando_label_ja": "高アルギニン血症",
    "nando_label_en": "Hyperargininemia",
    "mondo_id": "MONDO:0008814",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "アルギナーゼ欠損症",
    "mondo_label_en": "arginase deficiency",
    "mondo_url": "https://monarchinitiative.org/MONDO:0008814"
  },
  {
    "nando_id": "NANDO:2200481",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_2200481",
    "nando_label_ja": "アルギニノコハク酸尿症",
    "nando_label_en": "Argininosuccinic aciduria",
    "mondo_id": "MONDO:0008815",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "アルギニノコハク酸尿症",
    "mondo_label_en": "argininosuccinic aciduria",
    "mondo_url": "https://monarchinitiative.org/MONDO:0008815"
  },
  {
    "nando_id": "NANDO:2200511",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_2200511",
    "nando_label_ja": "カルニチン/アシルカルニチントランスロカーゼ欠損症",
    "nando_label_en": "Carnitine-acylcarnitine translocase deficiency",
    "mondo_id": "MONDO:0008918",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "カルニチン-アシルカルニチントランスロカーゼ欠損症",
    "mondo_label_en": "carnitine-acylcarnitine translocase deficiency",
    "mondo_url": "https://monarchinitiative.org/MONDO:0008918"
  },
  {
    "nando_id": "NANDO:2200508",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_2200508",
    "nando_label_ja": "全身性カルニチン欠損症",
    "nando_label_en": "Organic cation transporter 2 deficiency",
    "mondo_id": "MONDO:0008919",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "全身性原発性カルニチン欠乏症",
    "mondo_label_en": "systemic primary carnitine deficiency disease",
    "mondo_url": "https://monarchinitiative.org/MONDO:0008919"
  },
  {
    "nando_id": "NANDO:2200480",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_2200480",
    "nando_label_ja": "アルギニノコハク酸合成酵素欠損症",
    "nando_label_en": "Argininosuccinate synthetase deficiency",
    "mondo_id": "MONDO:0008988",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "シトルリン血症I型",
    "mondo_label_en": "citrullinemia type I",
    "mondo_url": "https://monarchinitiative.org/MONDO:0008988"
  },
  {
    "nando_id": "NANDO:2200362",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_2200362",
    "nando_label_ja": "見かけの鉱質コルチコイド過剰症候群",
    "nando_label_en": "Apparent mineralocorticoid excess syndrome",
    "mondo_id": "MONDO:0009025",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "見かけの鉱質コルチコイド過剰症",
    "mondo_label_en": "apparent mineralocorticoid excess",
    "mondo_url": "https://monarchinitiative.org/MONDO:0009025"
  },
  {
    "nando_id": "NANDO:2200353",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_2200353",
    "nando_label_ja": "副腎皮質結節性過形成",
    "nando_label_en": "ACTH-independent macronodular adrenal hyperplasia",
    "mondo_id": "MONDO:0009049",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "大結節性副腎皮質過形成によるクッシング症候群",
    "mondo_label_en": "Cushing syndrome due to macronodular adrenal hyperplasia",
    "mondo_url": "https://monarchinitiative.org/MONDO:0009049"
  },
  {
    "nando_id": "NANDO:2200350",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_2200350",
    "nando_label_ja": "クッシング病",
    "nando_label_en": "Cushing disease",
    "mondo_id": "MONDO:0009050",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "下垂体腺腫によるクッシング病",
    "mondo_label_en": "Cushing disease due to pituitary adenoma",
    "mondo_url": "https://monarchinitiative.org/MONDO:0009050"
  },
  {
    "nando_id": "NANDO:2200489",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_2200489",
    "nando_label_ja": "シスチン尿症",
    "nando_label_en": "Cystinuria",
    "mondo_id": "MONDO:0009067",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "シスチン尿症",
    "mondo_label_en": "cystinuria",
    "mondo_url": "https://monarchinitiative.org/MONDO:0009067"
  },
  {
    "nando_id": "NANDO:2200488",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_2200488",
    "nando_label_ja": "リジン尿性蛋白不耐症",
    "nando_label_en": "Lysinuric protein intolerance",
    "mondo_id": "MONDO:0009109",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "リジン尿性蛋白不耐症",
    "mondo_label_en": "lysinuric protein intolerance",
    "mondo_url": "https://monarchinitiative.org/MONDO:0009109"
  },
  {
    "nando_id": "NANDO:2200531",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_2200531",
    "nando_label_ja": "遺伝性フルクトース不耐症",
    "nando_label_en": "Hereditary fructose intolerance",
    "mondo_id": "MONDO:0009249",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "遺伝性フルクトース不耐症",
    "mondo_label_en": "hereditary fructose intolerance",
    "mondo_url": "https://monarchinitiative.org/MONDO:0009249"
  },
  {
    "nando_id": "NANDO:2200535",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_2200535",
    "nando_label_ja": "フルクトース-1,6-ビスホスファターゼ欠損症",
    "nando_label_en": "Fructose-1,6-bisphosphatase deficiency",
    "mondo_id": "MONDO:0009251",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "フルクトース-1,6-ビスホスファターゼ欠損症",
    "mondo_label_en": "fructose-1,6-bisphosphatase deficiency",
    "mondo_url": "https://monarchinitiative.org/MONDO:0009251"
  },
  {
    "nando_id": "NANDO:2200533",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_2200533",
    "nando_label_ja": "ガラクトキナーゼ欠損症",
    "nando_label_en": "Galactokinase deficiency",
    "mondo_id": "MONDO:0009255",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "ガラクトキナーゼ欠損症",
    "mondo_label_en": "galactokinase deficiency",
    "mondo_url": "https://monarchinitiative.org/MONDO:0009255"
  },
  {
    "nando_id": "NANDO:2200534",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_2200534",
    "nando_label_ja": "ウリジル二リン酸ガラクトース-4-エピメラーゼ欠損症",
    "nando_label_en": "UDP-galactose-4-epimerase deficiency",
    "mondo_id": "MONDO:0009257",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "ガラクトースエピメラーゼ欠損症",
    "mondo_label_en": "galactose epimerase deficiency",
    "mondo_url": "https://monarchinitiative.org/MONDO:0009257"
  },
  {
    "nando_id": "NANDO:2200532",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_2200532",
    "nando_label_ja": "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",
    "nando_label_en": "Galactose-1-phosphate uridyltransferase deficiency",
    "mondo_id": "MONDO:0009258",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "古典型ガラクトース血症",
    "mondo_label_en": "classic galactosemia",
    "mondo_url": "https://monarchinitiative.org/MONDO:0009258"
  },
  {
    "nando_id": "NANDO:2200501",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_2200501",
    "nando_label_ja": "グルタル酸血症1型",
    "nando_label_en": "Glutaric acidemia type 1",
    "mondo_id": "MONDO:0009281",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "グルタリルCoA脱水素酵素欠損症",
    "mondo_label_en": "glutaryl-CoA dehydrogenase deficiency",
    "mondo_url": "https://monarchinitiative.org/MONDO:0009281"
  },
  {
    "nando_id": "NANDO:2200502",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_2200502",
    "nando_label_ja": "グルタル酸血症2型",
    "nando_label_en": "Glutaric acidemia type 2",
    "mondo_id": "MONDO:0009282",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "マルチプルアシルCoA脱水素酵素欠損症",
    "mondo_label_en": "multiple acyl-CoA dehydrogenase deficiency",
    "mondo_url": "https://monarchinitiative.org/MONDO:0009282"
  },
  {
    "nando_id": "NANDO:2200539",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_2200539",
    "nando_label_ja": "糖原病III型",
    "nando_label_en": "Glycogen storage disease type III",
    "mondo_id": "MONDO:0009291",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "糖原病III",
    "mondo_label_en": "glycogen storage disease III",
    "mondo_url": "https://monarchinitiative.org/MONDO:0009291"
  },
  {
    "nando_id": "NANDO:2200540",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_2200540",
    "nando_label_ja": "糖原病IV型",
    "nando_label_en": "Glycogen storage disease type IV",
    "mondo_id": "MONDO:0009292",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "グリコーゲン分枝酵素欠損による糖原病",
    "mondo_label_en": "glycogen storage disease due to glycogen branching enzyme deficiency",
    "mondo_url": "https://monarchinitiative.org/MONDO:0009292"
  },
  {
    "nando_id": "NANDO:2200541",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_2200541",
    "nando_label_ja": "糖原病V型",
    "nando_label_en": "Glycogen storage disease type V",
    "mondo_id": "MONDO:0009293",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "糖原病V",
    "mondo_label_en": "glycogen storage disease V",
    "mondo_url": "https://monarchinitiative.org/MONDO:0009293"
  },
  {
    "nando_id": "NANDO:2200542",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_2200542",
    "nando_label_ja": "糖原病VI型",
    "nando_label_en": "Glycogen storage disease type VI",
    "mondo_id": "MONDO:0009294",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "糖原病VI",
    "mondo_label_en": "glycogen storage disease VI",
    "mondo_url": "https://monarchinitiative.org/MONDO:0009294"
  },
  {
    "nando_id": "NANDO:2200543",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_2200543",
    "nando_label_ja": "糖原病VII型",
    "nando_label_en": "Glycogen storage disease type VII",
    "mondo_id": "MONDO:0009295",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "糖原病VII",
    "mondo_label_en": "glycogen storage disease VII",
    "mondo_url": "https://monarchinitiative.org/MONDO:0009295"
  },
  {
    "nando_id": "NANDO:2200384",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_2200384",
    "nando_label_ja": "卵巣形成不全",
    "nando_label_en": "Ovarian dysgenesis",
    "mondo_id": "MONDO:0009299",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "46XX性腺異形成症",
    "mondo_label_en": "46 XX gonadal dysgenesis",
    "mondo_url": "https://monarchinitiative.org/MONDO:0009299"
  },
  {
    "nando_id": "NANDO:2200487",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_2200487",
    "nando_label_ja": "ハートナップ病",
    "nando_label_en": "Hartnup disease",
    "mondo_id": "MONDO:0009324",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "ハートナップ病",
    "mondo_label_en": "Hartnup disease",
    "mondo_url": "https://monarchinitiative.org/MONDO:0009324"
  },
  {
    "nando_id": "NANDO:2200478",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_2200478",
    "nando_label_ja": "カルバミルリン酸合成酵素欠損症",
    "nando_label_en": "Carbamoylphosphate synthetase deficiency",
    "mondo_id": "MONDO:0009376",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "カルバミルリン酸合成酵素I欠損症",
    "mondo_label_en": "carbamoyl phosphate synthetase I deficiency disease",
    "mondo_url": "https://monarchinitiative.org/MONDO:0009376"
  },
  {
    "nando_id": "NANDO:2200477",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_2200477",
    "nando_label_ja": "N-アセチルグルタミン酸合成酵素欠損症",
    "nando_label_en": "N-acetylglutamate synthetase deficiency",
    "mondo_id": "MONDO:0009377",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "Nアセチルグルタミン酸合成酵素欠損による高アンモニア血症",
    "mondo_label_en": "hyperammonemia due to N-acetylglutamate synthase deficiency",
    "mondo_url": "https://monarchinitiative.org/MONDO:0009377"
  },
  {
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    "mondo_label_ja": "免疫不全-動原体不安定性-顔面奇形症候群",
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    "mondo_label_ja": "脳動静脈奇形",
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    "nando_id": "NANDO:2200828",
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    "nando_label_ja": "ゴーリン症候群",
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    "mondo_id": "MONDO:0007187",
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    "mondo_label_ja": "母斑性基底細胞癌症候群",
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    "nando_id": "NANDO:2200870",
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    "mondo_label_ja": "セントラルコアミオパチー",
    "mondo_label_en": "central core myopathy",
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    "nando_id": "NANDO:2200845",
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    "mondo_id": "MONDO:0007405",
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    "mondo_label_ja": "クルーゾン症候群",
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    "nando_id": "NANDO:2200746",
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    "mondo_id": "MONDO:0008090",
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    "mondo_label_ja": "周期性好中球減少症",
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    "mondo_label_ja": "ハッチンソン・ギルフォード早老症候群",
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    "nando_id": "NANDO:2200668",
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    "mondo_id": "MONDO:0008332",
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    "mondo_label_ja": "血小板型フォン・ヴィレブランド病",
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    "nando_id": "NANDO:2200634",
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    "mondo_id": "MONDO:0008367",
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    "mondo_label_ja": "溶血を伴う赤血球リン脂質障害",
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    "nando_id": "NANDO:2200820",
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    "mondo_id": "MONDO:0008428",
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    "mondo_label_ja": "中隔視神経形成異常症",
    "mondo_label_en": "septooptic dysplasia",
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    "nando_id": "NANDO:2200830",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_2200830",
    "nando_label_ja": "スタージ・ウェーバー症候群",
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    "mondo_id": "MONDO:0008501",
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    "mondo_label_ja": "スタージ・ウェーバー症候群",
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    "nando_id": "NANDO:2200663",
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    "mondo_id": "MONDO:0008555",
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    "mondo_label_ja": "血小板減少症2",
    "mondo_label_en": "thrombocytopenia 2",
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    "nando_id": "NANDO:2200653",
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    "mondo_id": "MONDO:0008556",
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    "mondo_label_ja": "血小板減少症, 周期性",
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    "nando_id": "NANDO:2200645",
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    "mondo_id": "MONDO:0008558",
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    "mondo_label_ja": "自己免疫性血小板減少性紫斑病",
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  {
    "nando_id": "NANDO:2200829",
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    "mondo_id": "MONDO:0008667",
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    "mondo_label_ja": "フォンヒッペル・リンダウ病",
    "mondo_label_en": "von Hippel-Lindau disease",
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    "nando_id": "NANDO:2200604",
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    "mondo_id": "MONDO:0008692",
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    "mondo_label_ja": "無ベータリポ蛋白血症",
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    "nando_id": "NANDO:2200584",
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    "mondo_label_ja": "腸性肢端皮膚炎",
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    "nando_id": "NANDO:2200672",
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    "mondo_id": "MONDO:0008737",
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    "nando_id": "NANDO:2200835",
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    "nando_id": "NANDO:2200555",
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    "mondo_label_ja": "血管骨肥大症候群",
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    "nando_label_ja": "脊髄小脳失調症36型",
    "nando_label_en": "Spinocerebellar ataxia type 36",
    "mondo_id": "MONDO:0013594",
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    "nando_id": "NANDO:1200053",
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    "nando_id": "NANDO:1200054",
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    "nando_label_ja": "痙性対麻痺（複合型）",
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    "mondo_id": "MONDO:0015150",
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    "mondo_label_en": "complex hereditary spastic paraplegia",
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    "nando_id": "NANDO:1200168",
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    "nando_label_ja": "副腎脊髄ニューロパチー",
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    "mondo_id": "MONDO:0015339",
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    "mondo_label_ja": "副腎脊髄ニューロパチー",
    "mondo_label_en": "adrenomyeloneuropathy",
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    "mondo_id": "MONDO:0015626",
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    "mondo_label_ja": "シャルコー・マリー・トゥース病",
    "mondo_label_en": "Charcot-Marie-Tooth disease",
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    "nando_id": "NANDO:1200153",
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    "mondo_id": "MONDO:0015674",
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    "mondo_label_ja": "遅発性乳児型神経セロイドリポフスチン症",
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    "nando_id": "NANDO:1200187",
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    "nando_label_en": "Sporadic Creutzfeldt-Jakob disease",
    "mondo_id": "MONDO:0016079",
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    "mondo_label_ja": "孤発性クロイツフェルト・ヤコブ病",
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    "nando_id": "NANDO:1200075",
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    "nando_label_ja": "乳児型クラッベ病",
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    "mondo_id": "MONDO:0016089",
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    "mondo_label_ja": "乳児型クラッベ病",
    "mondo_label_en": "infantile Krabbe disease",
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    "nando_id": "NANDO:1200077",
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    "nando_label_ja": "成人型クラッベ病",
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    "mondo_id": "MONDO:0016091",
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    "mondo_label_ja": "成人型クラッベ病",
    "mondo_label_en": "adult Krabbe disease",
    "mondo_url": "https://monarchinitiative.org/MONDO:0016091"
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    "nando_id": "NANDO:1200161",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200161",
    "nando_label_ja": "シスチン症",
    "nando_label_en": "Cystinosis",
    "mondo_id": "MONDO:0016239",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "シスチン症",
    "mondo_label_en": "cystinosis",
    "mondo_url": "https://monarchinitiative.org/MONDO:0016239"
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    "nando_id": "NANDO:1200150",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200150",
    "nando_label_ja": "セロイドリポフスチノーシス",
    "nando_label_en": "Neuronal ceroid-lipofuscinosis",
    "mondo_id": "MONDO:0016295",
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    "mondo_label_ja": "神経セロイドリポフスチン症",
    "mondo_label_en": "neuronal ceroid lipofuscinosis",
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    "nando_id": "NANDO:1200065",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200065",
    "nando_label_ja": "成人型ニーマン・ピック病C型",
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    "mondo_id": "MONDO:0016310",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "ニーマン・ピック病C型, 成人期神経発症",
    "mondo_label_en": "Niemann-Pick disease type C, adult neurologic onset",
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    "nando_id": "NANDO:1200098",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200098",
    "nando_label_ja": "ハンター症候群（重症型）",
    "nando_label_en": "Hunter syndrome type A",
    "mondo_id": "MONDO:0016315",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "ムコ多糖症2型, 重症型",
    "mondo_label_en": "mucopolysaccharidosis type 2, severe form",
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    "nando_id": "NANDO:1200099",
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    "nando_label_ja": "ハンター症候群（軽症型）",
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    "mondo_id": "MONDO:0016316",
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    "mondo_label_ja": "ムコ多糖症2型, 軽症型",
    "mondo_label_en": "mucopolysaccharidosis type 2, attenuated form",
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    "nando_id": "NANDO:1200205",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200205",
    "nando_label_ja": "進行性多巣性白質脳症",
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    "mondo_id": "MONDO:0016318",
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    "mondo_label_ja": "進行性多巣性白質脳症",
    "mondo_label_en": "progressive multifocal leukoencephalopathy",
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    "nando_id": "NANDO:1200035",
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    "nando_label_ja": "MSA-C",
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    "mondo_id": "MONDO:0016418",
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    "mondo_label_ja": "多系統萎縮症, 小脳型",
    "mondo_label_en": "multiple system atrophy, cerebellar type",
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    "nando_id": "NANDO:1200028",
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    "nando_label_ja": "Baló病",
    "nando_label_en": "Baló concentric sclerosis",
    "mondo_id": "MONDO:0016430",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "バロー同心円性硬化症",
    "mondo_label_en": "Balo concentric sclerosis",
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    "nando_id": "NANDO:1200183",
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    "mondo_id": "MONDO:0016820",
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    "mondo_label_ja": "もやもや病",
    "mondo_label_en": "Moyamoya disease",
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    "mondo_id": "MONDO:0016987",
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    "mondo_label_ja": "神経有棘赤血球症",
    "mondo_label_en": "neuroacanthocytosis",
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    "nando_id": "NANDO:1200033",
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    "mondo_id": "MONDO:0017364",
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    "mondo_label_ja": "クロウ・深瀬症候群",
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    "nando_id": "NANDO:1200139",
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    "nando_label_ja": "乳児型ポンペ病",
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    "mondo_id": "MONDO:0017694",
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    "mondo_label_ja": "酸性マルターゼ欠損による糖原病, 乳児期発症",
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    "mondo_id": "MONDO:0017720",
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    "mondo_label_ja": "GM2ガングリオシドーシス",
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    "nando_id": "NANDO:1200079",
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    "mondo_id": "MONDO:0017729",
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    "mondo_label_ja": "異染性白質ジストロフィー, 乳幼児型",
    "mondo_label_en": "metachromatic leukodystrophy, late infantile form",
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    "mondo_id": "MONDO:0017730",
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    "mondo_label_ja": "異染性白質ジストロフィー, 成人型",
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    "nando_id": "NANDO:1200127",
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    "nando_id": "NANDO:1200116",
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    "mondo_label_ja": "シアリドーシス",
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    "mondo_label_ja": "アルファ-N-アセチルガラクトサミニダーゼ欠損症",
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    "nando_id": "NANDO:1200008",
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    "mondo_label_ja": "原発性側索硬化症",
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    "nando_id": "NANDO:1200165",
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    "mondo_id": "MONDO:0018544",
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    "mondo_label_ja": "副腎白質ジストロフィー",
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    "nando_id": "NANDO:1200192",
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    "mondo_label_ja": "獲得性クロイツフェルト・ヤコブ病",
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    "mondo_label_ja": "プロラクチン産生性下垂体腺腫",
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    "mondo_id": "MONDO:0010947",
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    "nando_label_ja": "オーメン症候群",
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    "mondo_id": "MONDO:0011338",
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    "mondo_label_ja": "オーメン症候群",
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    "nando_id": "NANDO:1200328",
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    "mondo_id": "MONDO:0011476",
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    "nando_id": "NANDO:1200430",
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    "mondo_id": "MONDO:0011705",
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    "mondo_label_ja": "リンパ脈管筋腫症",
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    "nando_id": "NANDO:1200361",
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    "mondo_id": "MONDO:0011888",
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    "mondo_label_ja": "免疫不全症67",
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    "nando_id": "NANDO:1200263",
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    "mondo_id": "MONDO:0012105",
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    "mondo_label_ja": "家族性虚血性大腿骨頭壊死",
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    "nando_id": "NANDO:1200326",
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    "mondo_id": "MONDO:0012197",
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    "nando_id": "NANDO:1200336",
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    "mondo_label_ja": "46,XY性逆転3",
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    "mondo_label_ja": "好酸球性胃腸炎",
    "mondo_label_en": "eosinophilic gastroenteritis",
    "mondo_url": "https://monarchinitiative.org/MONDO:0016129"
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    "nando_id": "NANDO:1200441",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200441",
    "nando_label_ja": "自己免疫性肝炎",
    "nando_label_en": "Autoimmune hepatitis",
    "mondo_id": "MONDO:0016264",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "自己免疫性肝炎",
    "mondo_label_en": "autoimmune hepatitis",
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  },
  {
    "nando_id": "NANDO:1200294",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200294",
    "nando_label_ja": "二次性拘束型心筋症",
    "nando_label_en": "Secondary restrictive cardiomyopathy",
    "mondo_id": "MONDO:0016345",
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    "mondo_label_ja": "非家族性拘束型心筋症",
    "mondo_label_en": "non-familial restrictive cardiomyopathy",
    "mondo_url": "https://monarchinitiative.org/MONDO:0016345"
  },
  {
    "nando_id": "NANDO:1200274",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200274",
    "nando_label_ja": "皮膚筋炎",
    "nando_label_en": "Dermatomyositis",
    "mondo_id": "MONDO:0016367",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "皮膚筋炎",
    "mondo_label_en": "dermatomyositis",
    "mondo_url": "https://monarchinitiative.org/MONDO:0016367"
  },
  {
    "nando_id": "NANDO:1200390",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200390",
    "nando_label_ja": "甲状腺刺激ホルモン分泌低下症",
    "nando_label_en": "Thyroid-stimulating hormone deficiency",
    "mondo_id": "MONDO:0016410",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "中枢性先天性甲状腺機能低下症",
    "mondo_label_en": "central congenital hypothyroidism",
    "mondo_url": "https://monarchinitiative.org/MONDO:0016410"
  },
  {
    "nando_id": "NANDO:1200355",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200355",
    "nando_label_ja": "白血球接着不全症",
    "nando_label_en": "Leukocyte adhesion deficiency",
    "mondo_id": "MONDO:0017570",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "白血球接着不全症",
    "mondo_label_en": "leukocyte adhesion deficiency",
    "mondo_url": "https://monarchinitiative.org/MONDO:0017570"
  },
  {
    "nando_id": "NANDO:1200458",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200458",
    "nando_label_ja": "慢性特発性偽性腸閉塞症",
    "nando_label_en": "Chronic idiopathic intestinal pseudo-obstruction",
    "mondo_id": "MONDO:0017574",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "慢性偽性腸閉塞",
    "mondo_label_en": "chronic intestinal pseudoobstruction",
    "mondo_url": "https://monarchinitiative.org/MONDO:0017574"
  },
  {
    "nando_id": "NANDO:1200235",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200235",
    "nando_label_ja": "単純型表皮水疱症",
    "nando_label_en": "Epidermolysis bullosa simplex",
    "mondo_id": "MONDO:0017610",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "単純型表皮水疱症",
    "mondo_label_en": "epidermolysis bullosa simplex",
    "mondo_url": "https://monarchinitiative.org/MONDO:0017610"
  },
  {
    "nando_id": "NANDO:1200236",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200236",
    "nando_label_ja": "接合部型表皮水疱症",
    "nando_label_en": "Junctional epidermolysis bullosa",
    "mondo_id": "MONDO:0017612",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "接合部型表皮水疱症",
    "mondo_label_en": "junctional epidermolysis bullosa",
    "mondo_url": "https://monarchinitiative.org/MONDO:0017612"
  },
  {
    "nando_id": "NANDO:1200352",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200352",
    "nando_label_ja": "自己免疫性リンパ増殖症候群",
    "nando_label_en": "Autoimmune lymphoproliferative syndrome",
    "mondo_id": "MONDO:0017979",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "自己免疫性リンパ増殖症候群",
    "mondo_label_en": "autoimmune lymphoproliferative syndrome",
    "mondo_url": "https://monarchinitiative.org/MONDO:0017979"
  },
  {
    "nando_id": "NANDO:1200251",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200251",
    "nando_label_ja": "高安動脈炎",
    "nando_label_en": "Takayasu arteritis",
    "mondo_id": "MONDO:0017991",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "高安動脈炎",
    "mondo_label_en": "Takayasu arteritis",
    "mondo_url": "https://monarchinitiative.org/MONDO:0017991"
  },
  {
    "nando_id": "NANDO:1200340",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200340",
    "nando_label_ja": "高IgE症候群",
    "nando_label_en": "Hyper-IgE syndrome",
    "mondo_id": "MONDO:0018037",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "高IgE症候群",
    "mondo_label_en": "hyper-IgE syndrome",
    "mondo_url": "https://monarchinitiative.org/MONDO:0018037"
  },
  {
    "nando_id": "NANDO:1200245",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200245",
    "nando_label_ja": "スティーヴンス・ジョンソン症候群",
    "nando_label_en": "Stevens-Johnson syndrome",
    "mondo_id": "MONDO:0018229",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "スティーヴンス・ジョンソン症候群",
    "mondo_label_en": "Stevens-Johnson syndrome",
    "mondo_url": "https://monarchinitiative.org/MONDO:0018229"
  },
  {
    "nando_id": "NANDO:1200357",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200357",
    "nando_label_ja": "慢性肉芽腫症",
    "nando_label_en": "Chronic granulomatous disease",
    "mondo_id": "MONDO:0018305",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "慢性肉芽腫症",
    "mondo_label_en": "chronic granulomatous disease",
    "mondo_url": "https://monarchinitiative.org/MONDO:0018305"
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  {
    "nando_id": "NANDO:1200394",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200394",
    "nando_label_ja": "家族性高コレステロール血症ホモ接合体",
    "nando_label_en": "Homozygous familial hypercholesterolemia",
    "mondo_id": "MONDO:0018328",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "ホモ接合性家族性高コレステロール血症",
    "mondo_label_en": "homozygous familial hypercholesterolemia",
    "mondo_url": "https://monarchinitiative.org/MONDO:0018328"
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  {
    "nando_id": "NANDO:1200454",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200454",
    "nando_label_ja": "好酸球性消化管疾患",
    "nando_label_en": "Eosinophilic gastrointestinal disorders",
    "mondo_id": "MONDO:0018438",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "好酸球性消化管疾患",
    "mondo_label_en": "eosinophilic gastrointestinal disease",
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    "nando_id": "NANDO:1200397",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200397",
    "nando_label_ja": "リポイド副腎過形成症",
    "nando_label_en": "Congenital lipoid adrenal hyperplasia",
    "mondo_id": "MONDO:0018479",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "先天性副腎皮質酵素欠損症",
    "mondo_label_en": "congenital adrenal hyperplasia",
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    "nando_id": "NANDO:1200353",
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    "nando_label_ja": "重症先天性好中球減少症",
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    "mondo_id": "MONDO:0018542",
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    "mondo_label_ja": "重症先天性好中球減少症",
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    "nando_id": "NANDO:1200426",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200426",
    "nando_label_ja": "肺静脈閉塞症／肺毛細血管腫症",
    "nando_label_en": "Pulmonary veno-occlusive disease / pulmonary capillary hemangiomatosis",
    "mondo_id": "MONDO:0018554",
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    "mondo_label_ja": "肺静脈閉塞症/肺毛細血管腫症",
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    "nando_id": "NANDO:1200388",
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    "nando_label_ja": "ゴナドトロピン分泌低下症",
    "nando_label_en": "Hypogonadotropic hypogonadism",
    "mondo_id": "MONDO:0018555",
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    "mondo_label_ja": "低ゴナドトロピン性性腺機能低下症",
    "mondo_label_en": "hypogonadotropic hypogonadism",
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    "nando_id": "NANDO:1200270",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200270",
    "nando_label_ja": "劇症型原発性抗リン脂質抗体症候群",
    "nando_label_en": "Catastrophic antiphospholipid syndrome",
    "mondo_id": "MONDO:0018737",
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    "mondo_label_ja": "劇症型原発性抗リン脂質抗体症候群",
    "mondo_label_en": "catastrophic antiphospholipid syndrome",
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    "nando_id": "NANDO:1200316",
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    "mondo_id": "MONDO:0018896",
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    "mondo_label_ja": "血栓性血小板減少性紫斑病",
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    "nando_id": "NANDO:1200307",
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    "mondo_id": "MONDO:0018922",
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    "mondo_label_ja": "寒冷凝集素症",
    "mondo_label_en": "cold agglutinin disease",
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    "nando_id": "NANDO:1200231",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200231",
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    "nando_label_en": "Paraneoplastic pemphigus",
    "mondo_id": "MONDO:0018974",
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    "mondo_label_ja": "腫瘍随伴性天疱瘡",
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    "nando_id": "NANDO:1200226",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200226",
    "nando_label_ja": "神経線維腫症I型",
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    "mondo_id": "MONDO:0018975",
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    "mondo_label_ja": "神経線維腫症1型",
    "mondo_label_en": "neurofibromatosis type 1",
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    "nando_id": "NANDO:1200262",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200262",
    "nando_label_ja": "顕微鏡的多発血管炎",
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    "mondo_id": "MONDO:0019124",
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    "mondo_label_ja": "顕微鏡的多発血管炎",
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    "nando_id": "NANDO:1200283",
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    "mondo_id": "MONDO:0019125",
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    "mondo_label_ja": "再発性多発軟骨炎",
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    "nando_id": "NANDO:1200276",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200276",
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    "mondo_id": "MONDO:0019127",
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    "mondo_label_ja": "多発性筋炎",
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    "nando_id": "NANDO:1200359",
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    "mondo_id": "MONDO:0019146",
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    "nando_id": "NANDO:1200381",
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    "mondo_id": "MONDO:0019165",
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    "mondo_label_ja": "中枢性思春期早発症",
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    "nando_id": "NANDO:1200261",
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    "mondo_id": "MONDO:0019170",
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    "mondo_label_ja": "結節性多発動脈炎",
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    "nando_id": "NANDO:1200431",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200431",
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    "mondo_id": "MONDO:0019200",
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    "mondo_label_ja": "網膜色素変性症",
    "mondo_label_en": "retinitis pigmentosa",
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    "nando_id": "NANDO:1200420",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200420",
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    "mondo_id": "MONDO:0019203",
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    "mondo_label_ja": "急性間質性肺炎",
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    "nando_id": "NANDO:1200232",
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    "nando_label_en": "Pemphigus vegetans",
    "mondo_id": "MONDO:0019322",
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    "mondo_label_ja": "増殖性天疱瘡",
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    "nando_id": "NANDO:1200233",
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    "nando_label_en": "Pemphigus erythematosus",
    "mondo_id": "MONDO:0019323",
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    "mondo_label_ja": "紅斑性天疱瘡",
    "mondo_label_en": "pemphigus erythematosus",
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    "nando_id": "NANDO:1200230",
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    "nando_label_en": "Pemphigus foliaceus",
    "mondo_id": "MONDO:0019324",
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    "mondo_label_ja": "落葉状天疱瘡",
    "mondo_label_en": "pemphigus foliaceus",
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    "nando_id": "NANDO:1200415",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200415",
    "nando_label_ja": "サルコイドーシス",
    "nando_label_en": "Sarcoidosis",
    "mondo_id": "MONDO:0019338",
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    "mondo_label_ja": "サルコイドーシス",
    "mondo_label_en": "sarcoidosis",
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    "nando_id": "NANDO:1200282",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200282",
    "nando_label_ja": "成人発症スチル病",
    "nando_label_en": "Adult-onset Still disease",
    "mondo_id": "MONDO:0019355",
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    "mondo_label_ja": "成人スチル病",
    "mondo_label_en": "adult-onset Still disease",
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    "nando_label_ja": "レット症候群",
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    "mondo_label_ja": "熱性感染症関連てんかん症候群",
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    "mondo_id": "MONDO:0016532",
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    "nando_id": "NANDO:1200543",
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    "mondo_label_ja": "ドーパ反応性ジストニア",
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    "mondo_label_ja": "点頭てんかん",
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    "mondo_label_ja": "ウォルフラム症候群",
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    "mondo_label_ja": "KID症候群",
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    "nando_label_ja": "22q11.2欠失症候群",
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    "nando_label_ja": "アルポート症候群",
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    "nando_id": "NANDO:1200758",
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    "mondo_label_ja": "バース症候群",
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    "mondo_id": "MONDO:0011214",
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    "mondo_id": "MONDO:0011612",
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    "mondo_label_ja": "グリシン脳症",
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    "nando_id": "NANDO:1200862",
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    "nando_label_ja": "三頭酵素欠損症",
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    "mondo_label_ja": "Kleefstra症候群",
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    "mondo_label_ja": "周期熱-乳児腸炎-自己炎症症候群",
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    "nando_label_ja": "複合カルボキシラーゼ欠損症",
    "nando_label_en": "Multiple carboxylase deficiency",
    "mondo_id": "MONDO:0015454",
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    "mondo_label_ja": "複合カルボキシラーゼ欠損症",
    "mondo_label_en": "multiple carboxylase deficiency",
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    "nando_label_ja": "カルニチンパルミトイルトランスフェラーゼII欠損症",
    "nando_label_en": "Carnitine palmitoyltransferase II deficiency",
    "mondo_id": "MONDO:0015515",
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    "mondo_id": "MONDO:0015762",
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    "mondo_label_ja": "進行性家族性肝内胆汁うっ滞",
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    "nando_id": "NANDO:1200937",
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    "nando_label_ja": "錐体杆体ジストロフィー",
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    "mondo_id": "MONDO:0015993",
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    "mondo_label_ja": "錐体-杆体ジストロフィー",
    "mondo_label_en": "cone-rod dystrophy",
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    "nando_id": "NANDO:1200960",
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    "nando_label_ja": "コルネリア・デランゲ症候群",
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    "mondo_id": "MONDO:0016033",
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    "mondo_label_ja": "コルネリアデランゲ症候群",
    "mondo_label_en": "Cornelia de Lange syndrome",
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    "nando_id": "NANDO:1201010",
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    "mondo_id": "MONDO:0016356",
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    "mondo_label_ja": "びまん皮膚硬化型全身性強皮症",
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    "nando_id": "NANDO:1201011",
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    "nando_label_ja": "限局皮膚硬化型全身性強皮症",
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    "mondo_id": "MONDO:0016358",
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    "mondo_label_ja": "限局皮膚硬化型全身性強皮症",
    "mondo_label_en": "limited cutaneous systemic sclerosis",
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  {
    "nando_id": "NANDO:1200944",
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    "nando_label_ja": "アッシャー症候群3型",
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    "mondo_id": "MONDO:0016485",
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    "mondo_label_ja": "アッシャー症候群1型",
    "mondo_label_en": "Usher syndrome type 3",
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  {
    "nando_id": "NANDO:1200978",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200978",
    "nando_label_ja": "シトリン欠損症",
    "nando_label_en": "Citrin deficiency",
    "mondo_id": "MONDO:0016602",
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    "mondo_label_ja": "シトリン欠損症",
    "mondo_label_en": "citrin deficiency",
    "mondo_url": "https://monarchinitiative.org/MONDO:0016602"
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    "nando_id": "NANDO:1200980",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200980",
    "nando_label_ja": "成人発症II型シトルリン血症",
    "nando_label_en": "Adult-onset type II citrullinemia",
    "mondo_id": "MONDO:0016603",
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    "mondo_label_ja": "シトルリン血症II型",
    "mondo_label_en": "citrullinemia type II",
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    "nando_id": "NANDO:1200958",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200958",
    "nando_label_ja": "1q部分重複症候群",
    "nando_label_en": "Partial trisomy 1q",
    "mondo_id": "MONDO:0016952",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "1番染色体長腕部分重複",
    "mondo_label_en": "partial duplication of the long arm of chromosome 1",
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  {
    "nando_id": "NANDO:1200874",
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    "nando_label_ja": "タナトフォリック骨異形成症",
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    "mondo_id": "MONDO:0017042",
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    "mondo_label_ja": "タナトフォリック骨異形成症",
    "mondo_label_en": "thanatophoric dysplasia",
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    "nando_id": "NANDO:1200998",
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    "nando_label_ja": "大理石骨病",
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    "mondo_id": "MONDO:0017198",
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    "mondo_label_ja": "大理石骨病",
    "mondo_label_en": "osteopetrosis",
    "mondo_url": "https://monarchinitiative.org/MONDO:0017198"
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    "nando_id": "NANDO:1200923",
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    "mondo_id": "MONDO:0017287",
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    "mondo_label_ja": "IgG4関連硬化性疾患",
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    "nando_id": "NANDO:1200985",
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    "nando_label_ja": "新生児型非ケトーシス型高グリシン血症",
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    "mondo_label_ja": "新生児グリシン脳症",
    "mondo_label_en": "neonatal glycine encephalopathy",
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    "nando_id": "NANDO:1200986",
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    "mondo_id": "MONDO:0017354",
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    "mondo_label_ja": "乳児グリシン脳症",
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    "nando_id": "NANDO:1200989",
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    "mondo_label_ja": "3-メチルグルタコン酸尿症",
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    "nando_id": "NANDO:1200969",
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    "mondo_id": "MONDO:0017716",
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    "mondo_label_ja": "カルニチン回路・カルニチン輸送障害",
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    "mondo_label_ja": "家族性地中海熱",
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    "nando_id": "NANDO:1200903",
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    "mondo_label_ja": "ヒルシュスプルング病",
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    "nando_id": "NANDO:1200996",
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    "nando_label_ja": "エカルディ・グティエール症候群",
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    "mondo_label_ja": "アイカルディ・ゴーティエ症候群",
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    "nando_id": "NANDO:1200859",
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    "nando_id": "NANDO:1200852",
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    "mondo_id": "MONDO:0018999",
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    "nando_id": "NANDO:1201036",
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    "mondo_label_ja": "後天性血友病",
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    "mondo_label_ja": "先天性全身性リポジストロフィー",
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    "nando_id": "NANDO:1200933",
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    "nando_id": "NANDO:1200891",
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    "mondo_id": "MONDO:0019391",
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    "mondo_label_ja": "ファンコーニ貧血",
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    "nando_id": "NANDO:1200885",
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    "nando_label_en": "Congenital dyserythropoietic anemia",
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    "mondo_label_ja": "先天性赤血球形成異常性貧血",
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    "nando_id": "NANDO:2200110",
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    "nando_label_ja": "フィンランド型先天性ネフローゼ症候群",
    "nando_label_en": "Congenital nephrotic syndrome of the Finnish type",
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    "mondo_label_ja": "先天性ネフローゼ症候群, フィンランド型",
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    "nando_id": "NANDO:2200048",
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    "nando_label_ja": "骨肉腫",
    "nando_label_en": "Osteosarcoma",
    "mondo_id": "MONDO:0009807",
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    "mondo_url": "https://monarchinitiative.org/MONDO:0015863"
  },
  {
    "nando_id": "NANDO:2200071",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_2200071",
    "nando_label_ja": "混合性胚細胞腫瘍",
    "nando_label_en": "Mixed germ cell tumour",
    "mondo_id": "MONDO:0015864",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "混合型胚細胞腫瘍",
    "mondo_label_en": "mixed germ cell tumor",
    "mondo_url": "https://monarchinitiative.org/MONDO:0015864"
  },
  {
    "nando_id": "NANDO:2100132",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_2100132",
    "nando_label_ja": "低アルドステロン症",
    "nando_label_en": "Hypoaldosteronism",
    "mondo_id": "MONDO:0015900",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "低アルドステロン症",
    "mondo_label_en": "hypoaldosteronism disease",
    "mondo_url": "https://monarchinitiative.org/MONDO:0015900"
  },
  {
    "nando_id": "NANDO:2100283",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_2100283",
    "nando_label_ja": "先天性魚鱗癬",
    "nando_label_en": "Congenital ichthyosis",
    "mondo_id": "MONDO:0015947",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "遺伝性魚鱗癬",
    "mondo_label_en": "inherited ichthyosis",
    "mondo_url": "https://monarchinitiative.org/MONDO:0015947"
  },
  {
    "nando_id": "NANDO:2200158",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_2200158",
    "nando_label_ja": "多嚢胞性異形成腎",
    "nando_label_en": "Multicystic dysplastic kidney",
    "mondo_id": "MONDO:0015988",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "多嚢胞性異形成腎",
    "mondo_label_en": "multicystic dysplastic kidney",
    "mondo_url": "https://monarchinitiative.org/MONDO:0015988"
  },
  {
    "nando_id": "NANDO:2200131",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_2200131",
    "nando_label_ja": "非典型溶血性尿毒症症候群",
    "nando_label_en": "Atypical hemolytic uremic syndrome",
    "mondo_id": "MONDO:0016244",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "非典型溶血性尿毒症症候群",
    "mondo_label_en": "atypical hemolytic-uremic syndrome",
    "mondo_url": "https://monarchinitiative.org/MONDO:0016244"
  },
  {
    "nando_id": "NANDO:2200159",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_2200159",
    "nando_label_ja": "寡巨大糸球体症",
    "nando_label_en": "Oligomeganephronia",
    "mondo_id": "MONDO:0016407",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "寡巨大糸球体症",
    "mondo_label_en": "oligomeganephronia",
    "mondo_url": "https://monarchinitiative.org/MONDO:0016407"
  },
  {
    "nando_id": "NANDO:1201096",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1201096",
    "nando_label_ja": "線毛機能不全症候群（カルタゲナー症候群を含む。）",
    "nando_label_en": "Primary ciliary dyskinesia (including Kartagener syndrome)",
    "mondo_id": "MONDO:0016575",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "原発性線毛機能不全症",
    "mondo_label_en": "primary ciliary dyskinesia",
    "mondo_url": "https://monarchinitiative.org/MONDO:0016575"
  },
  {
    "nando_id": "NANDO:2200203",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_2200203",
    "nando_label_ja": "線毛機能不全症候群",
    "nando_label_en": "Primary ciliary dyskinesia",
    "mondo_id": "MONDO:0016575",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "原発性線毛機能不全症",
    "mondo_label_en": "primary ciliary dyskinesia",
    "mondo_url": "https://monarchinitiative.org/MONDO:0016575"
  },
  {
    "nando_id": "NANDO:2200230",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_2200230",
    "nando_label_ja": "不整脈源性右室心筋症",
    "nando_label_en": "Arrhythmogenic right ventricular cardiomyopathy or dysplasia",
    "mondo_id": "MONDO:0016587",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "不整脈源性右室心筋症",
    "mondo_label_en": "arrhythmogenic right ventricular cardiomyopathy",
    "mondo_url": "https://monarchinitiative.org/MONDO:0016587"
  },
  {
    "nando_id": "NANDO:2200094",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_2200094",
    "nando_label_ja": "髄膜腫",
    "nando_label_en": "Meningioma",
    "mondo_id": "MONDO:0016642",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "髄膜腫",
    "mondo_label_en": "meningioma",
    "mondo_url": "https://monarchinitiative.org/MONDO:0016642"
  },
  {
    "nando_id": "NANDO:2200086",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_2200086",
    "nando_label_ja": "退形成性星細胞腫",
    "nando_label_en": "Anaplastic astrocytoma",
    "mondo_id": "MONDO:0016684",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "退形成性星細胞腫",
    "mondo_label_en": "anaplastic astrocytoma",
    "mondo_url": "https://monarchinitiative.org/MONDO:0016684"
  },
  {
    "nando_id": "NANDO:2200085",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_2200085",
    "nando_label_ja": "びまん性星細胞腫",
    "nando_label_en": "Diffuse astrocytoma",
    "mondo_id": "MONDO:0016686",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "びまん性星細胞腫",
    "mondo_label_en": "diffuse astrocytoma",
    "mondo_url": "https://monarchinitiative.org/MONDO:0016686"
  },
  {
    "nando_id": "NANDO:2200084",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_2200084",
    "nando_label_ja": "毛様細胞性星細胞腫",
    "nando_label_en": "Pilocytic astrocytoma",
    "mondo_id": "MONDO:0016691",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "毛様細胞性星細胞腫",
    "mondo_label_en": "pilocytic astrocytoma",
    "mondo_url": "https://monarchinitiative.org/MONDO:0016691"
  },
  {
    "nando_id": "NANDO:2200089",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_2200089",
    "nando_label_ja": "乏突起神経膠腫",
    "nando_label_en": "Oligodendroglioma",
    "mondo_id": "MONDO:0016695",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "乏突起神経膠腫",
    "mondo_label_en": "oligodendroglioma",
    "mondo_url": "https://monarchinitiative.org/MONDO:0016695"
  },
  {
    "nando_id": "NANDO:2200088",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_2200088",
    "nando_label_ja": "上衣腫",
    "nando_label_en": "Ependymoma",
    "mondo_id": "MONDO:0016698",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "上衣腫",
    "mondo_label_en": "ependymoma",
    "mondo_url": "https://monarchinitiative.org/MONDO:0016698"
  },
  {
    "nando_id": "NANDO:2200092",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_2200092",
    "nando_label_ja": "松果体腫",
    "nando_label_en": "Pineocytoma",
    "mondo_id": "MONDO:0016723",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "松果体腫",
    "mondo_label_en": "pineocytoma",
    "mondo_url": "https://monarchinitiative.org/MONDO:0016723"
  },
  {
    "nando_id": "NANDO:2200097",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_2200097",
    "nando_label_ja": "神経節腫",
    "nando_label_en": "Gangliocytoma",
    "mondo_id": "MONDO:0016730",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "神経節細胞腫",
    "mondo_label_en": "gangliocytoma",
    "mondo_url": "https://monarchinitiative.org/MONDO:0016730"
  },
  {
    "nando_id": "NANDO:2200096",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_2200096",
    "nando_label_ja": "神経節膠腫",
    "nando_label_en": "Ganglioglioma",
    "mondo_id": "MONDO:0016733",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "神経節膠腫",
    "mondo_label_en": "ganglioglioma",
    "mondo_url": "https://monarchinitiative.org/MONDO:0016733"
  },
  {
    "nando_id": "NANDO:2100148",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_2100148",
    "nando_label_ja": "多発性内分泌腫瘍",
    "nando_label_en": "Multiple endocrine neoplasia",
    "mondo_id": "MONDO:0017169",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "多発性内分泌腫瘍",
    "mondo_label_en": "multiple endocrine neoplasia",
    "mondo_url": "https://monarchinitiative.org/MONDO:0017169"
  },
  {
    "nando_id": "NANDO:2100125",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_2100125",
    "nando_label_ja": "自己免疫性多内分泌腺症候群",
    "nando_label_en": "Autoimmune polyendocrinopathy",
    "mondo_id": "MONDO:0017278",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "自己免疫性多発性内分泌症",
    "mondo_label_en": "autoimmune polyendocrinopathy",
    "mondo_url": "https://monarchinitiative.org/MONDO:0017278"
  },
  {
    "nando_id": "NANDO:1201074",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1201074",
    "nando_label_ja": "孔脳症",
    "nando_label_en": "Porencephaly",
    "mondo_id": "MONDO:0017410",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "孔脳症",
    "mondo_label_en": "porencephaly",
    "mondo_url": "https://monarchinitiative.org/MONDO:0017410"
  },
  {
    "nando_id": "NANDO:2200102",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_2200102",
    "nando_label_ja": "悪性神経鞘腫",
    "nando_label_en": "Malignant neurinoma",
    "mondo_id": "MONDO:0017827",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "悪性腹膜神経鞘腫",
    "mondo_label_en": "malignant peripheral nerve sheath tumor",
    "mondo_url": "https://monarchinitiative.org/MONDO:0017827"
  },
  {
    "nando_id": "NANDO:1201049",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1201049",
    "nando_label_ja": "セニオール・ローケン症候群",
    "nando_label_en": "Senior-Loken syndrome",
    "mondo_id": "MONDO:0017842",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "Senior-Loken症候群",
    "mondo_label_en": "Senior-Loken syndrome",
    "mondo_url": "https://monarchinitiative.org/MONDO:0017842"
  },
  {
    "nando_id": "NANDO:2200010",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_2200010",
    "nando_label_ja": "急性赤白血病",
    "nando_label_en": "Acute erythremia",
    "mondo_id": "MONDO:0017858",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "急性赤白血病",
    "mondo_label_en": "acute erythroid leukemia",
    "mondo_url": "https://monarchinitiative.org/MONDO:0017858"
  },
  {
    "nando_id": "NANDO:2200221",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_2200221",
    "nando_label_ja": "カテコラミン誘発多形性心室頻拍",
    "nando_label_en": "Catecholaminergic polymorphic ventricular tachycardia",
    "mondo_id": "MONDO:0017990",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "カテコラミン誘発多形性心室頻拍",
    "mondo_label_en": "catecholaminergic polymorphic ventricular tachycardia",
    "mondo_url": "https://monarchinitiative.org/MONDO:0017990"
  },
  {
    "nando_id": "NANDO:2200038",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_2200038",
    "nando_label_ja": "エルドハイム・チェスター病",
    "nando_label_en": "Erdheim-Chester disease",
    "mondo_id": "MONDO:0018153",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "エルドハイム・チェスター病",
    "mondo_label_en": "Erdheim-Chester disease",
    "mondo_url": "https://monarchinitiative.org/MONDO:0018153"
  },
  {
    "nando_id": "NANDO:2200087",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_2200087",
    "nando_label_ja": "膠芽腫",
    "nando_label_en": "Glioblastoma",
    "mondo_id": "MONDO:0018177",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "膠芽腫",
    "mondo_label_en": "glioblastoma",
    "mondo_url": "https://monarchinitiative.org/MONDO:0018177"
  },
  {
    "nando_id": "NANDO:2200055",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_2200055",
    "nando_label_ja": "末梢性未分化神経外胚葉性腫瘍",
    "nando_label_en": "Peripheral primitive neuroectodermal tumors",
    "mondo_id": "MONDO:0018271",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "未分化神経外胚葉性腫瘍（末梢性のものに限る。）",
    "mondo_label_en": "peripheral primitive neuroectodermal tumor",
    "mondo_url": "https://monarchinitiative.org/MONDO:0018271"
  },
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    "nando_id": "NANDO:2100241",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_2100241",
    "nando_label_ja": "脳の鉄沈着を伴う神経変性疾患",
    "nando_label_en": "Neurodegeneration with brain iron accumulation",
    "mondo_id": "MONDO:0018307",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "脳内鉄沈着神経変性症",
    "mondo_label_en": "neurodegeneration with brain iron accumulation",
    "mondo_url": "https://monarchinitiative.org/MONDO:0018307"
  },
  {
    "nando_id": "NANDO:2200031",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_2200031",
    "nando_label_ja": "ランゲルハンス細胞組織球症",
    "nando_label_en": "Langerhans cell histiocytosis",
    "mondo_id": "MONDO:0018310",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "ランゲルハンス細胞組織球症",
    "mondo_label_en": "Langerhans cell histiocytosis",
    "mondo_url": "https://monarchinitiative.org/MONDO:0018310"
  },
  {
    "nando_id": "NANDO:2200156",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_2200156",
    "nando_label_ja": "腎無形成",
    "nando_label_en": "Renal aplasia",
    "mondo_id": "MONDO:0018470",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "腎無発生",
    "mondo_label_en": "renal agenesis",
    "mondo_url": "https://monarchinitiative.org/MONDO:0018470"
  },
  {
    "nando_id": "NANDO:2200046",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_2200046",
    "nando_label_ja": "肝芽腫",
    "nando_label_en": "Hepatoblastoma",
    "mondo_id": "MONDO:0018666",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "肝芽腫",
    "mondo_label_en": "hepatoblastoma",
    "mondo_url": "https://monarchinitiative.org/MONDO:0018666"
  },
  {
    "nando_id": "NANDO:1201072",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1201072",
    "nando_label_ja": "敷石様皮質異形成",
    "nando_label_en": "Cobblestone brain malformation",
    "mondo_id": "MONDO:0018869",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "敷石様皮質異形成",
    "mondo_label_en": "cobblestone lissencephaly",
    "mondo_url": "https://monarchinitiative.org/MONDO:0018869"
  },
  {
    "nando_id": "NANDO:2200011",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_2200011",
    "nando_label_ja": "急性巨核芽球性白血病",
    "nando_label_en": "Acute megakaryoblastic leukemia",
    "mondo_id": "MONDO:0018872",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "急性巨核芽球性白血病",
    "mondo_label_en": "acute megakaryoblastic leukemia",
    "mondo_url": "https://monarchinitiative.org/MONDO:0018872"
  },
  {
    "nando_id": "NANDO:2200019",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_2200019",
    "nando_label_ja": "骨髄異形成症候群",
    "nando_label_en": "Myelodysplastic syndrome",
    "mondo_id": "MONDO:0018881",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "骨髄異形成症候群",
    "mondo_label_en": "myelodysplastic syndrome",
    "mondo_url": "https://monarchinitiative.org/MONDO:0018881"
  },
  {
    "nando_id": "NANDO:2200091",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_2200091",
    "nando_label_ja": "頭蓋咽頭腫",
    "nando_label_en": "Craniopharyngioma",
    "mondo_id": "MONDO:0018907",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "頭蓋咽頭腫",
    "mondo_label_en": "craniopharyngioma",
    "mondo_url": "https://monarchinitiative.org/MONDO:0018907"
  },
  {
    "nando_id": "NANDO:2200184",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_2200184",
    "nando_label_ja": "巨大尿管症",
    "nando_label_en": "Megaureter",
    "mondo_id": "MONDO:0018960",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "先天性原発性巨大尿管症",
    "mondo_label_en": "congenital primary megaureter",
    "mondo_url": "https://monarchinitiative.org/MONDO:0018960"
  },
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    "nando_id": "NANDO:2200126",
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    "nando_label_ja": "バルデー・ビードル症候群",
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    "nando_id": "NANDO:2200263",
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    "nando_label_ja": "先天性下垂体機能低下症",
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    "mondo_id": "MONDO:0018800",
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    "mondo_id": "MONDO:0018997",
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    "mondo_id": "MONDO:0019003",
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    "nando_id": "NANDO:2200426",
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    "mondo_id": "MONDO:0019124",
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    "nando_id": "NANDO:2200391",
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    "mondo_id": "MONDO:0019161",
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    "mondo_label_ja": "OTC欠損症",
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    "mondo_label_ja": "NBIA４",
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    "nando_label_ja": "オーメン症候群",
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    "nando_label_ja": "プリンヌクレオシドホスホリラーゼ欠損症",
    "nando_label_en": "Purine nucleoside phosphorylase deficiency",
    "mondo_id": "MONDO:0013171",
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    "mondo_label_ja": "プリンヌクレオシドホスホリラーゼ欠損症",
    "mondo_label_en": "purine nucleoside phosphorylase deficiency",
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    "nando_id": "NANDO:2200688",
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    "nando_label_ja": "先天性プラスミノゲンアクチベータインヒビター1欠乏症",
    "nando_label_en": "Congenital plasminogen activator inhibitor-1 deficiency",
    "mondo_id": "MONDO:0013227",
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    "mondo_label_ja": "先天性プラスミノーゲン活性化阻害因子1型欠損症",
    "mondo_label_en": "congenital plasminogen activator inhibitor type 1 deficiency",
    "mondo_url": "https://monarchinitiative.org/MONDO:0013227"
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    "nando_id": "NANDO:2200739",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_2200739",
    "nando_label_ja": "ITCH欠損症",
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    "mondo_id": "MONDO:0013245",
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    "mondo_label_ja": "ITCH欠損による症候性多臓器自己免疫疾患",
    "mondo_label_en": "syndromic multisystem autoimmune disease due to ITCH deficiency",
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    "nando_id": "NANDO:2200777",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_2200777",
    "nando_label_ja": "C1q 欠損症",
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    "mondo_id": "MONDO:0013343",
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    "mondo_label_ja": "C1q欠損症",
    "mondo_label_en": "C1Q deficiency",
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    "nando_id": "NANDO:2200741",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_2200741",
    "nando_label_ja": "FADD欠損症",
    "nando_label_en": "Fas-associated death domain protein deficiency",
    "mondo_id": "MONDO:0013408",
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    "mondo_label_ja": "FADD関連免疫不全症",
    "mondo_label_en": "FADD-related immunodeficiency",
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    "nando_id": "NANDO:2200782",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_2200782",
    "nando_label_ja": "C3 欠損症",
    "nando_label_en": "C3 deficiency",
    "mondo_id": "MONDO:0013417",
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    "mondo_label_ja": "補体第3成分欠損症",
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    "nando_id": "NANDO:2200779",
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    "nando_label_ja": "C1s 欠損症",
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    "mondo_id": "MONDO:0013419",
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    "mondo_label_ja": "補体成分C1s欠損症",
    "mondo_label_en": "complement component C1s deficiency",
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    "nando_id": "NANDO:2200793",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_2200793",
    "nando_label_ja": "MASP2 欠損症",
    "nando_label_en": "MASP2 deficiency",
    "mondo_id": "MONDO:0013423",
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    "mondo_label_ja": "MASP2欠損による免疫不全症",
    "mondo_label_en": "immunodeficiency due to MASP-2 deficiency",
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    "nando_id": "NANDO:2200787",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_2200787",
    "nando_label_ja": "C9 欠損症",
    "nando_label_en": "C9 deficiency",
    "mondo_id": "MONDO:0013445",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "補体第9成分欠損症",
    "mondo_label_en": "complement component 9 deficiency",
    "mondo_url": "https://monarchinitiative.org/MONDO:0013445"
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    "nando_id": "NANDO:2200794",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_2200794",
    "nando_label_ja": "Ficolin3 関連免疫不全症",
    "nando_label_en": "Ficolin 3 Deficiency",
    "mondo_id": "MONDO:0013467",
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    "mondo_label_ja": "フィコリン3関連免疫不全症",
    "mondo_label_en": "immunodeficiency due to ficolin3 deficiency",
    "mondo_url": "https://monarchinitiative.org/MONDO:0013467"
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  {
    "nando_id": "NANDO:2200788",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_2200788",
    "nando_label_ja": "Factor D 欠損症",
    "nando_label_en": "Factor D deficiency",
    "mondo_id": "MONDO:0013487",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "D因子欠損によるナイセリア反復感染",
    "mondo_label_en": "recurrent Neisseria infections due to factor D deficiency",
    "mondo_url": "https://monarchinitiative.org/MONDO:0013487"
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    "nando_id": "NANDO:2200719",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_2200719",
    "nando_label_ja": "IgGサブクラス欠損症",
    "nando_label_en": "Isolated IgG subclass deficiency",
    "mondo_id": "MONDO:0013576",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "希少免疫グロブリンアイソタイプ欠乏に関連する反復感染",
    "mondo_label_en": "recurrent infections associated with rare immunoglobulin isotypes deficiency",
    "mondo_url": "https://monarchinitiative.org/MONDO:0013576"
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    "nando_id": "NANDO:2200801",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_2200801",
    "nando_label_ja": "CR2欠損症",
    "nando_label_en": "CD21 deficiency",
    "mondo_id": "MONDO:0013862",
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    "mondo_label_ja": "免疫不全症, 分類不能型, 7",
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    "nando_id": "NANDO:2200797",
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    "nando_label_ja": "B因子欠損症",
    "nando_label_en": "Factor B deficiency",
    "mondo_id": "MONDO:0014255",
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    "mondo_label_ja": "B因子欠損症",
    "mondo_label_en": "complement factor b deficiency",
    "mondo_url": "https://monarchinitiative.org/MONDO:0014255"
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    "nando_id": "NANDO:2200766",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_2200766",
    "nando_label_ja": "HOIL1欠損症",
    "nando_label_en": "HOIL-1 deficiency",
    "mondo_id": "MONDO:0014389",
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    "mondo_label_ja": "免疫不全を伴うまたは伴わないポリグルコサン小体ミオパチー1",
    "mondo_label_en": "polyglucosan body myopathy 1 with or without immunodeficiency",
    "mondo_url": "https://monarchinitiative.org/MONDO:0014389"
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  {
    "nando_id": "NANDO:2200770",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_2200770",
    "nando_label_ja": "STAT2欠損症",
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    "mondo_id": "MONDO:0014715",
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    "mondo_label_ja": "麻疹・ムンプス・風疹ワクチン後ウイルス感染を伴う原発性免疫不全症",
    "mondo_label_en": "primary immunodeficiency with post-measles-mumps-rubella vaccine viral infection",
    "mondo_url": "https://monarchinitiative.org/MONDO:0014715"
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    "nando_id": "NANDO:2200764",
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    "nando_label_ja": "慢性皮膚粘膜カンジダ症",
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    "mondo_id": "MONDO:0015279",
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    "nando_id": "NANDO:2200824",
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    "mondo_id": "MONDO:0015369",
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    "nando_id": "NANDO:2200717",
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    "mondo_label_ja": "分類不能型免疫不全症",
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    "nando_id": "NANDO:2200806",
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    "nando_label_ja": "特発性好酸球増加症",
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    "mondo_id": "MONDO:0015691",
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    "mondo_label_ja": "好酸球増加症候群",
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    "nando_id": "NANDO:2200722",
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    "mondo_id": "MONDO:0015698",
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    "mondo_label_ja": "乳児一過性低ガンマグロブリン血症",
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    "nando_label_ja": "先天性角化異常症",
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    "mondo_label_ja": "先天性角化異常症",
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    "nando_id": "NANDO:2200693",
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    "mondo_id": "MONDO:0015909",
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    "mondo_label_ja": "再生不良性貧血",
    "mondo_label_en": "aplastic anemia",
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    "nando_id": "NANDO:2200832",
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    "nando_label_ja": "コケイン症候群",
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    "mondo_label_ja": "コケイン症候群",
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    "nando_id": "NANDO:2200819",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_2200819",
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    "nando_id": "NANDO:2200822",
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    "mondo_id": "MONDO:0016349",
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    "nando_id": "NANDO:2200813",
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    "mondo_label_ja": "髄膜脳瘤",
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    "nando_id": "NANDO:2200792",
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    "nando_label_ja": "3MC 症候群",
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    "nando_id": "NANDO:2200755",
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    "nando_id": "NANDO:2200726",
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    "nando_id": "NANDO:2200713",
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    "mondo_label_ja": "高IgE症候群",
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    "nando_id": "NANDO:2200686",
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    "nando_id": "NANDO:2200757",
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    "mondo_label_ja": "慢性肉芽腫症",
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    "nando_id": "NANDO:2200807",
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    "mondo_label_ja": "重症先天性好中球減少症",
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    "mondo_label_ja": "滑脳症スペクトラム障害",
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    "mondo_label_ja": "甲状腺髄様癌",
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    "mondo_label_ja": "びまん性リンパ管奇形",
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    "mondo_id": "MONDO:0017729",
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    "mondo_label_ja": "異染性白質ジストロフィー, 乳幼児型",
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    "nando_id": "NANDO:2201204",
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    "mondo_id": "MONDO:0017730",
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    "mondo_label_ja": "異染性白質ジストロフィー, 成人型",
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    "nando_id": "NANDO:2201188",
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    "mondo_id": "MONDO:0017732",
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    "mondo_label_ja": "α-マンノシドーシス型, 乳児型",
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    "nando_id": "NANDO:2201189",
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    "mondo_id": "MONDO:0017733",
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    "nando_id": "NANDO:2201238",
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    "nando_label_ja": "中間型遊離シアル酸蓄積症",
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    "mondo_id": "MONDO:0017737",
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    "mondo_label_ja": "中間型重症サラ病",
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    "nando_id": "NANDO:2201006",
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    "nando_label_ja": "スティーヴンス・ジョンソン症候群",
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    "mondo_id": "MONDO:0018229",
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    "nando_id": "NANDO:2201021",
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    "mondo_id": "MONDO:0018240",
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    "mondo_label_ja": "ＴＲＰＶ４関連骨障害",
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    "nando_id": "NANDO:2201255",
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    "mondo_id": "MONDO:0018328",
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    "mondo_label_ja": "ホモ接合性家族性高コレステロール血症",
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    "nando_id": "NANDO:2201012",
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    "nando_label_ja": "低ホスファターゼ症",
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    "mondo_label_ja": "低ホスファターゼ症",
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    "mondo_label_ja": "KID症候群",
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    "nando_id": "NANDO:2201003",
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    "mondo_id": "MONDO:0018975",
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    "mondo_label_ja": "神経線維腫症1型",
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    "mondo_label_ja": "ピリドキシン依存性てんかん",
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    "mondo_id": "MONDO:0019534",
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    "nando_id": "NANDO:1200608",
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    "nando_id": "NANDO:1200760",
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    "mondo_label_ja": "Zellweger症候群",
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    "mondo_id": "MONDO:0019622",
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    "nando_id": "NANDO:1200365",
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    "mondo_id": "MONDO:0019623",
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    "nando_id": "NANDO:1200783",
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    "mondo_id": "MONDO:0019642",
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    "mondo_id": "MONDO:0019731",
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    "mondo_label_ja": "AApoAIアミロイドーシス",
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    "mondo_id": "MONDO:0019736",
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    "mondo_id": "MONDO:0019740",
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    "nando_label_ja": "無甲状腺症",
    "nando_label_en": "Thyroid agenesis",
    "mondo_id": "MONDO:0019855",
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    "mondo_label_ja": "無甲状腺症",
    "mondo_label_en": "athyreosis",
    "mondo_url": "https://monarchinitiative.org/MONDO:0019855"
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    "nando_id": "NANDO:2200315",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_2200315",
    "nando_label_ja": "先端巨大症",
    "nando_label_en": "Acromegaly",
    "mondo_id": "MONDO:0019933",
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    "mondo_label_ja": "先端巨大症",
    "mondo_label_en": "acromegaly",
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    "nando_id": "NANDO:2200875",
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    "mondo_id": "MONDO:0019948",
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    "mondo_label_ja": "還元小体ミオパチー",
    "mondo_label_en": "reducing body myopathy",
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  {
    "nando_id": "NANDO:2200397",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_2200397",
    "nando_label_ja": "グルカゴノーマ",
    "nando_label_en": "Glucagonoma",
    "mondo_id": "MONDO:0019959",
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    "mondo_label_ja": "グルカゴノーマ",
    "mondo_label_en": "glucagonoma",
    "mondo_url": "https://monarchinitiative.org/MONDO:0019959"
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  {
    "nando_id": "NANDO:2200394",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_2200394",
    "nando_label_ja": "VIP産生腫瘍",
    "nando_label_en": "Vipoma",
    "mondo_id": "MONDO:0019960",
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    "mondo_label_ja": "VIP産生腫瘍",
    "mondo_label_en": "VIPoma",
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  {
    "nando_id": "NANDO:2200171",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_2200171",
    "nando_label_ja": "多房性腎嚢胞",
    "nando_label_en": "Multilocular cysts of the kidney",
    "mondo_id": "MONDO:0019983",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "多房性腎嚢胞",
    "mondo_label_en": "multiloculated renal cyst",
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  {
    "nando_id": "NANDO:2200349",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_2200349",
    "nando_label_ja": "偽性副甲状腺機能低下症",
    "nando_label_en": "Pseudohypoparathyroidism",
    "mondo_id": "MONDO:0019992",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "偽性副甲状腺機能低下症",
    "mondo_label_en": "pseudohypoparathyroidism",
    "mondo_url": "https://monarchinitiative.org/MONDO:0019992"
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  {
    "nando_id": "NANDO:2200282",
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    "nando_label_ja": "一側肺動脈欠損",
    "nando_label_en": "Unilateral absence of a pulmonary artery",
    "mondo_id": "MONDO:0020007",
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    "mondo_label_ja": "一側肺動脈欠損",
    "mondo_label_en": "absence of the pulmonary artery",
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  {
    "nando_id": "NANDO:2200118",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_2200118",
    "nando_label_ja": "中枢神経奇形症候群",
    "nando_label_en": "Central nervous system malformation syndrome",
    "mondo_id": "MONDO:0020022",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "中枢神経奇形症候群",
    "mondo_label_en": "central nervous system malformation",
    "mondo_url": "https://monarchinitiative.org/MONDO:0020022"
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  {
    "nando_id": "NANDO:2200393",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_2200393",
    "nando_label_ja": "46,XX性分化疾患",
    "nando_label_en": "Disorders of sex development of 46,XX",
    "mondo_id": "MONDO:0020040",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "46,XY性分化疾患",
    "mondo_label_en": "46,XY disorder of sex development",
    "mondo_url": "https://monarchinitiative.org/MONDO:0020040"
  },
  {
    "nando_id": "NANDO:2200280",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_2200280",
    "nando_label_ja": "肺動脈弁欠損",
    "nando_label_en": "Absent pulmonary valve",
    "mondo_id": "MONDO:0020064",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "肺動脈弁欠損",
    "mondo_label_en": "pulmonary valve agenesis",
    "mondo_url": "https://monarchinitiative.org/MONDO:0020064"
  },
  {
    "nando_id": "NANDO:2200607",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_2200607",
    "nando_label_ja": "エーラス・ダンロス症候群",
    "nando_label_en": "Ehlers-Danlos syndrome",
    "mondo_id": "MONDO:0020066",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "エーラス・ダンロス症候群",
    "mondo_label_en": "Ehlers-Danlos syndrome",
    "mondo_url": "https://monarchinitiative.org/MONDO:0020066"
  },
  {
    "nando_id": "NANDO:2200623",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_2200623",
    "nando_label_ja": "口唇赤血球症",
    "nando_label_en": "Hereditary stomatocytosis",
    "mondo_id": "MONDO:0020102",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "遺伝性口唇赤血球症",
    "mondo_label_en": "hereditary stomatocytosis",
    "mondo_url": "https://monarchinitiative.org/MONDO:0020102"
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  {
    "nando_id": "NANDO:2200014",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_2200014",
    "nando_label_ja": "慢性骨髄単球性白血病",
    "nando_label_en": "Chronic myelomonocytic leukemia",
    "mondo_id": "MONDO:0020311",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "慢性骨髄単球性白血病",
    "mondo_label_en": "chronic myelomonocytic leukemia",
    "mondo_url": "https://monarchinitiative.org/MONDO:0020311"
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  {
    "nando_id": "NANDO:2200017",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_2200017",
    "nando_label_ja": "急性未分化型白血病",
    "nando_label_en": "Acute undifferentiated leukemia",
    "mondo_id": "MONDO:0020321",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "急性未分化型白血病",
    "mondo_label_en": "acute undifferentiated leukemia",
    "mondo_url": "https://monarchinitiative.org/MONDO:0020321"
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  {
    "nando_id": "NANDO:2200021",
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    "nando_label_ja": "未分化大細胞リンパ腫",
    "nando_label_en": "Anaplastic large cell lymphoma",
    "mondo_id": "MONDO:0020325",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "未分化大細胞リンパ腫",
    "mondo_label_en": "anaplastic large cell lymphoma",
    "mondo_url": "https://monarchinitiative.org/MONDO:0020325"
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  {
    "nando_id": "NANDO:2200613",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_2200613",
    "nando_label_ja": "後天性赤芽球癆",
    "nando_label_en": "Acquired pure red cell aplasia",
    "mondo_id": "MONDO:0020338",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "後天性赤芽球癆",
    "mondo_label_en": "adult pure red cell aplasia",
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    "nando_id": "NANDO:2200281",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_2200281",
    "nando_label_ja": "肺動脈上行大動脈起始症",
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    "mondo_id": "MONDO:0020391",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "肺動脈上行大動脈起始症",
    "mondo_label_en": "pulmonary artery coming from the aorta",
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  {
    "nando_id": "NANDO:2200308",
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    "nando_label_ja": "僧帽弁弁上輪",
    "nando_label_en": "Supramitral ring",
    "mondo_id": "MONDO:0020400",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "先天性僧帽弁弁上輪",
    "mondo_label_en": "congenital supravalvular mitral ring",
    "mondo_url": "https://monarchinitiative.org/MONDO:0020400"
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    "nando_id": "NANDO:2200290",
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    "nando_label_ja": "重複大動脈弓症",
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    "mondo_id": "MONDO:0020413",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "重複大動脈弓症",
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    "nando_id": "NANDO:2200274",
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    "nando_label_ja": "左室右房交通症",
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    "mondo_id": "MONDO:0020428",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "左室右房交通症",
    "mondo_label_en": "congenital Gerbode defect",
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    "nando_id": "NANDO:2200266",
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    "mondo_id": "MONDO:0020434",
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    "mondo_label_ja": "心房中隔欠損症, 二次孔型",
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    "nando_id": "NANDO:2200267",
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    "mondo_id": "MONDO:0020436",
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    "mondo_label_ja": "心房中隔欠損症, 静脈洞型",
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    "nando_id": "NANDO:2200272",
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    "mondo_id": "MONDO:0020453",
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    "mondo_label_ja": "部分肺静脈還流異常症",
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    "nando_id": "NANDO:2200625",
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    "mondo_id": "MONDO:0020459",
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    "mondo_label_ja": "不安定ヘモグロビン症",
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    "nando_id": "NANDO:2200314",
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    "mondo_id": "MONDO:0020479",
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    "mondo_label_ja": "下垂体性巨人症",
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    "nando_id": "NANDO:2200812",
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    "nando_id": "NANDO:2200101",
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    "mondo_id": "MONDO:0020560",
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    "mondo_id": "MONDO:0020586",
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    "mondo_id": "MONDO:0020587",
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    "nando_id": "NANDO:2200152",
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    "nando_id": "NANDO:2200988",
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    "mondo_id": "MONDO:0020702",
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    "mondo_label_ja": "常染色体顕性表皮融解性魚鱗癬",
    "mondo_label_en": "autosomal dominant epidermolytic ichthyosis",
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    "nando_id": "NANDO:2200018",
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    "mondo_label_ja": "混合型急性白血病",
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    "nando_id": "NANDO:2200915",
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    "nando_id": "NANDO:2201317",
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    "mondo_id": "MONDO:0021081",
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    "mondo_label_ja": "抗NMDA受容体脳炎",
    "mondo_label_en": "anti-NMDA receptor encephalitis",
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    "nando_id": "NANDO:2200236",
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    "mondo_id": "MONDO:0021209",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "心臓腫瘍",
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    "nando_id": "NANDO:2200262",
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    "mondo_label_ja": "ドラベ症候群",
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    "nando_label_ja": "進行性家族性肝内胆汁うっ滞症　その他の型",
    "nando_label_en": "Progressive Familial Intrahepatic Cholestasis, other types",
    "mondo_id": "MONDO:0018804",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "MYO5B関連進行性家族性肝内胆汁うっ滞",
    "mondo_label_en": "MYO5B-related progressive familial intrahepatic cholestasis",
    "mondo_url": "https://monarchinitiative.org/MONDO:0018804"
  },
  {
    "nando_id": "NANDO:1201163",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1201163",
    "nando_label_ja": "コケイン症候群I型",
    "nando_label_en": "Cockayne syndrome type 1",
    "mondo_id": "MONDO:0019569",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "コケイン症候群1型",
    "mondo_label_en": "Cockayne syndrome type 1",
    "mondo_url": "https://monarchinitiative.org/MONDO:0019569"
  },
  {
    "nando_id": "NANDO:1201164",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1201164",
    "nando_label_ja": "コケイン症候群II型",
    "nando_label_en": "Cockayne syndrome type 2",
    "mondo_id": "MONDO:0019570",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "コケイン症候群2型",
    "mondo_label_en": "Cockayne syndrome type 2",
    "mondo_url": "https://monarchinitiative.org/MONDO:0019570"
  },
  {
    "nando_id": "NANDO:1201160",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1201160",
    "nando_label_ja": "ファイファー症候群1型",
    "nando_label_en": "Pfeiffer syndrome type 1",
    "mondo_id": "MONDO:0019659",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "ファイファー症候群1型",
    "mondo_label_en": "Pfeiffer syndrome type 1",
    "mondo_url": "https://monarchinitiative.org/MONDO:0019659"
  },
  {
    "nando_id": "NANDO:1201161",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1201161",
    "nando_label_ja": "ファイファー症候群2型",
    "nando_label_en": "Pfeiffer syndrome type 2",
    "mondo_id": "MONDO:0019660",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "ファイファー症候群2型",
    "mondo_label_en": "Pfeiffer syndrome type 2",
    "mondo_url": "https://monarchinitiative.org/MONDO:0019660"
  },
  {
    "nando_id": "NANDO:1201162",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1201162",
    "nando_label_ja": "ファイファー症候群3型",
    "nando_label_en": "Pfeiffer syndrome type 3",
    "mondo_id": "MONDO:0019661",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "ファイファー症候群3型",
    "mondo_label_en": "Pfeiffer syndrome type 3",
    "mondo_url": "https://monarchinitiative.org/MONDO:0019661"
  },
  {
    "nando_id": "NANDO:2201533",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_2201533",
    "nando_label_ja": "続発性脊髄空洞症",
    "nando_label_en": "secondary syringomyelia",
    "mondo_id": "MONDO:0020509",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "二次性脊髄空洞症",
    "mondo_label_en": "secondary syringomyelia",
    "mondo_url": "https://monarchinitiative.org/MONDO:0020509"
  },
  {
    "nando_id": "NANDO:1201149",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1201149",
    "nando_label_ja": "DYT30 ジストニア",
    "nando_label_en": "DYT30 Dystonia",
    "mondo_id": "MONDO:0025691",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "ジストニア30",
    "mondo_label_en": "dystonia 30",
    "mondo_url": "https://monarchinitiative.org/MONDO:0025691"
  },
  {
    "nando_id": "NANDO:1200601",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200601",
    "nando_label_ja": "睡眠時棘徐波活性化を示す発達性てんかん性脳症およびてんかん性脳症",
    "nando_label_en": "Developmental and/or epileptic encephalopathy with spike-wave activation in sleep",
    "mondo_id": "MONDO:0800501",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "睡眠時に棘徐波活性化を示す発達性てんかん性脳症",
    "mondo_label_en": "developmental and/or epileptic encephalopathy with spike-wave activation in sleep",
    "mondo_url": "https://monarchinitiative.org/MONDO:0800501"
  }
]