{
  "id": 14682,
  "label": "intellectual disability, autosomal dominant 11",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0013658",
  "properties": {
    "xrefs": [
      "DOID:0070041",
      "GARD:0016461",
      "MEDGEN:481915",
      "OMIM:614257",
      "UMLS:C3280285"
    ],
    "synonyms": [
      "EPB41L1 autosomal dominant non-syndromic intellectual disability",
      "MRD11",
      "autosomal dominant intellectual disability 11",
      "autosomal dominant non-syndromic intellectual disability caused by mutation in EPB41L1",
      "intellectual developmental disorder, autosomal dominant 11",
      "intellectual disability, autosomal dominant 11",
      "intellectual disability, autosomal dominant type 11",
      "mental retardation, autosomal dominant type 11",
      "autosomal dominant non-syndromic intellectual disability 11",
      "mental retardation, autosomal dominant 11"
    ],
    "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 EPB41L1 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"
    }
  ]
}