{
  "id": 8825,
  "label": "dentatorubral-pallidoluysian atrophy",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0007435",
  "properties": {
    "xrefs": [
      "DOID:0060162",
      "GARD:0005643",
      "ICD9:333.99",
      "MEDGEN:155630",
      "NANDO:1200043",
      "NCIT:C122653",
      "OMIM:125370",
      "Orphanet:101",
      "SCTID:68116008",
      "UMLS:C0751781"
    ],
    "synonyms": [
      "DRPLA",
      "Dentatorubropallidoluysian atrophy",
      "Naito-Oyanagi disease",
      "dentatorubral-pallidoluysian atrophy",
      "haw River syndrome",
      "NOD",
      "Naito Oyanagi disease",
      "ataxia, chorea, seizures, and dementia",
      "dentatorubral pallidoluysian atrophy",
      "myoclonic epilepsy with choreoathetosis"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "Dentatorubral pallidoluysian atrophy (DRPLA) is a rare subtype of type I autosomal dominant cerebellar ataxia (ADCA type I). It is characterized by involuntary movements, ataxia, epilepsy, mental disorders, cognitive decline and prominent anticipation."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 16361,
      "label": "Huntington disease-like syndrome",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        2754,
        16360
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0020029",
          "ICD9:333.99",
          "MEDGEN:777988",
          "MESH:C580174",
          "Orphanet:158266",
          "SCTID:702376003",
          "UMLS:C3711380"
        ],
        "synonyms": [
          "Huntington disease phenocopy syndrome"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 20,
      "reference_id": "MONDO:0015548"
    },
    {
      "id": 19537,
      "label": "autosomal dominant cerebellar ataxia type IV",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        19840
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0019254",
          "MEDGEN:1842584",
          "Orphanet:94149",
          "UMLS:C5680261"
        ],
        "synonyms": [
          "ADCA4",
          "ADCAIV",
          "autosomal dominant cerebellar ataxia type 4",
          "autosomal dominant cerebellar ataxia type IV"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 2,
      "reference_id": "MONDO:0019794"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 16361,
      "label": "Huntington disease-like syndrome"
    },
    {
      "id": 19537,
      "label": "autosomal dominant cerebellar ataxia type IV"
    }
  ]
}