{
  "id": 15673,
  "label": "intellectual disability, autosomal dominant 39",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0014678",
  "properties": {
    "xrefs": [
      "DOID:0070069",
      "GARD:0027861",
      "MEDGEN:909304",
      "OMIM:616521",
      "UMLS:C4225296"
    ],
    "synonyms": [
      "MRD39",
      "MYT1L autosomal dominant non-syndromic intellectual disability",
      "autosomal dominant intellectual disability 39",
      "autosomal dominant non-syndromic intellectual disability caused by mutation in MYT1L",
      "intellectual developmental disorder, autosomal dominant 39",
      "intellectual disability, autosomal dominant 39",
      "intellectual disability, autosomal dominant type 39",
      "mental retardation, autosomal dominant type 39",
      "mental retardation, autosomal dominant 39"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "Any autosomal dominant non-syndromic intellectual disability in which the cause of the disease is a mutation in the MYT1L gene."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 23914,
      "label": "intellectual disability, autosomal dominant",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        2903,
        3324,
        24226
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "OMIMPS:156200"
        ],
        "synonyms": [
          "mental retardation, autosomal dominant",
          "autosomal dominant intellectual disability"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 87,
      "reference_id": "MONDO:0100172"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 23914,
      "label": "intellectual disability, autosomal dominant"
    }
  ]
}