{
  "id": 29328,
  "label": "complex movement disorder with or without neurodevelopmental features",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:1060159",
  "properties": {
    "synonyms": [
      "complex movement disorder with or without neurodevelopmental features"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "A movement disorder characterized by having one or more different types of movement disorders, such as abnormal muscle tone, abnormal degree of movement, dystonia or torsion, which may occur with or without neurodevelopmental features, such as developmental delay or intellectual disability."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 1,
  "parents": [
    {
      "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": 10385,
      "label": "torsion dystonia 2",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        16634,
        29328
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0090038",
          "GARD:0002028",
          "MEDGEN:346511",
          "MESH:C538006",
          "NANDO:1200513",
          "NCIT:C123415",
          "OMIM:224500",
          "Orphanet:99657",
          "UMLS:C1857093"
        ],
        "synonyms": [
          "DYT2",
          "HPCA dystonic disorder",
          "autosomal recessive torsion dystonia 2",
          "dystonic disorder caused by mutation in HPCA",
          "torsion dystonia type 2",
          "dystonia 2, torsion, autosomal recessive",
          "dystonia musculorum deformans type 2",
          "torsion dystonia 2, autosomal recessive type"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A dystonia characterized by segmental dystonia that predominantly affects the distal limbs and leads to abnormal posture. This disease has a progressive clinical course and may develop into generalized dystonia but remains mild overall."
      },
      "child_count": 0,
      "reference_id": "MONDO:0009141"
    }
  ],
  "roots": [
    {
      "id": 7073,
      "label": "movement disorder"
    }
  ]
}