{
  "id": 15826,
  "label": "intellectual disability, autosomal dominant 41",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0014842",
  "properties": {
    "xrefs": [
      "DOID:0070071",
      "GARD:0025023",
      "MEDGEN:934751",
      "OMIM:616944",
      "UMLS:C4310784"
    ],
    "synonyms": [
      "MRD41",
      "TBL1XR1 autosomal dominant non-syndromic intellectual disability",
      "autosomal dominant intellectual disability 41",
      "autosomal dominant non-syndromic intellectual disability caused by mutation in TBL1XR1",
      "intellectual disability, autosomal dominant 41",
      "intellectual disability, autosomal dominant type 41",
      "mental retardation, autosomal dominant 41",
      "mental retardation, autosomal dominant type 41",
      "autosomal dominant non-syndromic intellectual disability 41"
    ],
    "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 TBL1XR1 gene."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 16555,
      "label": "autosomal dominant non-syndromic intellectual disability",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        2962,
        23914
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0060307",
          "GARD:0012107",
          "MEDGEN:1826082",
          "Orphanet:178469",
          "UMLS:C5680502"
        ],
        "synonyms": [
          "autosomal dominant mental retardation",
          "autosomal dominant non-syndromic intellectual disability",
          "non-syndromic intellectual disability, autosomal dominant"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Autosomal dominant form of non-syndromic intellectual disability."
      },
      "child_count": 52,
      "reference_id": "MONDO:0015802"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 16555,
      "label": "autosomal dominant non-syndromic intellectual disability"
    }
  ]
}