{
  "id": 15359,
  "label": "intellectual disability, autosomal dominant 24",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0014357",
  "properties": {
    "xrefs": [
      "DOID:0070054",
      "GARD:0016467",
      "MEDGEN:862851",
      "OMIM:615828",
      "UMLS:C4014414"
    ],
    "synonyms": [
      "DEAF1 autosomal dominant non-syndromic intellectual disability",
      "MRD24",
      "autosomal dominant intellectual disability 24",
      "autosomal dominant non-syndromic intellectual disability caused by mutation in DEAF1",
      "intellectual disability, autosomal dominant 24",
      "intellectual disability, autosomal dominant type 24",
      "mental retardation, autosomal dominant type 24",
      "autosomal dominant non-syndromic intellectual disability 24",
      "mental retardation, autosomal dominant 24"
    ],
    "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 DEAF1 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"
    },
    {
      "id": 25031,
      "label": "DEAF1-associated neurodevelopmental disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        23791,
        24226
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0027072"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A neurodevelopmental disorder characterized predominantly by intellectual disability, speech delay, motor delay, autism, sleep disturbances, and a high pain threshold. This disorder may be inherited in an autosomal dominant or autosomal recessive manner, likely due to mono-allelic variant resulting in altered function and bi-allelic variants resulting in loss of function, respectively."
      },
      "child_count": 4,
      "reference_id": "MONDO:0800443"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 23914,
      "label": "intellectual disability, autosomal dominant"
    },
    {
      "id": 25031,
      "label": "DEAF1-associated neurodevelopmental disorder"
    }
  ]
}