{
  "id": 23683,
  "label": "neurodevelopmental disorder with involuntary movements",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0060491",
  "properties": {
    "xrefs": [
      "DOID:0112276",
      "GARD:0016232",
      "GARD:0022369",
      "ICD10CM:F84.8",
      "MEDGEN:1374697",
      "MEDGEN:1830103",
      "OMIM:617493",
      "Orphanet:592564",
      "UMLS:C4479569",
      "UMLS:C5680303"
    ],
    "synonyms": [
      "GNAO1-related developmental delay-seizures-movement disorder spectrum",
      "GNAO1-related spectrum",
      "neurodevelopmental disorder with involuntary movements",
      "NEDIM"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 24226,
      "label": "Mendelian neurodevelopmental disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        24270,
        24488
      ],
      "type_id": 0,
      "properties": {
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A neurodevelopmental disorder that is caused by genetic modifications where those modifications are inherited from a parent's genome."
      },
      "child_count": 550,
      "reference_id": "MONDO:0100500"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 24226,
      "label": "Mendelian neurodevelopmental disorder"
    }
  ]
}