{
  "id": 25399,
  "label": "intellectual developmental disorder with language impairment and early-onset DOPA-responsive dystonia-parkinsonism",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0859257",
  "properties": {
    "xrefs": [
      "GARD:0027148",
      "MEDGEN:1805453",
      "OMIM:619911",
      "Orphanet:660017",
      "UMLS:C5677001"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ]
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 1,
  "parents": [
    {
      "id": 26027,
      "label": "autosomal dominant dopa-responsive dystonia",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        17241,
        18954,
        23452
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0027165",
          "Orphanet:98808",
          "icd11.foundation:1143673207"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A rare neurometabolic disorder characterized by childhood-onset dystonia that shows a dramatic and sustained response to low doses of levodopa (L-dopa) and that may be associated with parkinsonism at an older age."
      },
      "child_count": 6,
      "reference_id": "MONDO:0971063"
    }
  ],
  "children": [
    {
      "id": 26026,
      "label": "developmental delay-language impairment-dopa responsive dystonia-parkinsonism syndrome due to a NR4A2 point mutation",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        25399
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0027164",
          "MEDGEN:1863959",
          "Orphanet:660012",
          "UMLS:C5925124"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "An intellectual developmental disorder with language impairment and early-onset DOPA-responsive dystonia-parkinsonism in which the cause of the disease is a point mutation in the gene NR4A2."
      },
      "child_count": 0,
      "reference_id": "MONDO:0971062"
    }
  ],
  "roots": [
    {
      "id": 26027,
      "label": "autosomal dominant dopa-responsive dystonia"
    }
  ]
}