{
  "id": 9090,
  "label": "Huntington disease",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0007739",
  "properties": {
    "xrefs": [
      "DOID:12858",
      "GARD:0006677",
      "ICD10CM:G10",
      "ICD10WHO:G10",
      "ICD9:333.4",
      "MEDGEN:5654",
      "MESH:D006816",
      "MedDRA:10070668",
      "NANDO:1200012",
      "NCIT:C82342",
      "NORD:1256",
      "OMIM:143100",
      "Orphanet:399",
      "SCTID:58756001",
      "UMLS:C0020179",
      "icd11.foundation:2132180242"
    ],
    "synonyms": [
      "HD",
      "Huntington chorea",
      "Huntington disease",
      "Huntington's Disease",
      "Huntington's chorea",
      "Huntington's disease"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "Huntington disease (HD) is a rare neurodegenerative disorder of the central nervous system characterized by unwanted choreatic movements, behavioral and psychiatric disturbances and dementia."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 2,
  "parents": [
    {
      "id": 2754,
      "label": "Huntington disease and related disorders",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        21292
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0022721"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A grouping for Huntington disease and similar diseases."
      },
      "child_count": 2,
      "reference_id": "MONDO:0000167"
    },
    {
      "id": 7073,
      "label": "movement disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6799
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:480",
          "EFO:0004280",
          "ICD9:333.90",
          "ICD9:333.99",
          "MEDGEN:10113",
          "MESH:D009069",
          "NCIT:C116757",
          "SCTID:60342002",
          "UMLS:C0026650"
        ],
        "synonyms": [
          "movement disease",
          "movement disorder",
          "movement disorders"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Neurological conditions resulting in abnormal voluntary or involuntary movement, which may impact the speed, fluency, quality and ease of movement."
      },
      "child_count": 54,
      "reference_id": "MONDO:0005395"
    }
  ],
  "children": [
    {
      "id": 17105,
      "label": "juvenile Huntington disease",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        9090
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0010510",
          "MEDGEN:155518",
          "NCIT:C147072",
          "Orphanet:248111",
          "SCTID:230299004",
          "UMLS:C0751208"
        ],
        "synonyms": [
          "JHD",
          "juvenile Huntington chorea",
          "Huntington disease, juvenile onset",
          "juvenile onset HD"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Juvenile Huntington disease (JHD) is a form of Huntington disease (HD), characterized by onset of signs and symptoms before 20 years of age."
      },
      "child_count": 0,
      "reference_id": "MONDO:0016621"
    },
    {
      "id": 23104,
      "label": "Westphal disease",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        9090
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0005557",
          "GTR:AN0099343",
          "GTR:AN0099344",
          "GTR:AN0099345",
          "MEDGEN:224821",
          "MESH:C536694",
          "SCTID:182747006",
          "UMLS:C1279186"
        ],
        "synonyms": [
          "Westphal disease",
          "HD- Westphal variant",
          "Westphal variant of Huntington's disease"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0042980"
    }
  ],
  "roots": [
    {
      "id": 2754,
      "label": "Huntington disease and related disorders"
    },
    {
      "id": 7073,
      "label": "movement disorder"
    }
  ]
}