{
  "id": 15613,
  "label": "intellectual disability, autosomal dominant 38",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0014617",
  "properties": {
    "xrefs": [
      "DOID:0070068",
      "GARD:0016469",
      "MEDGEN:895359",
      "OMIM:616393",
      "UMLS:C4225343"
    ],
    "synonyms": [
      "EEF1A2 autosomal dominant non-syndromic intellectual disability",
      "MRD38",
      "PRELDS",
      "autosomal dominant intellectual disability 38",
      "autosomal dominant non-syndromic intellectual disability caused by mutation in EEF1A2",
      "intellectual disability, autosomal dominant 38",
      "intellectual disability, autosomal dominant type 38",
      "mental retardation, autosomal dominant type 38",
      "psychomotor retardation, epilepsy, and language disability syndrome",
      "autosomal dominant non-syndromic intellectual disability 38",
      "mental retardation, autosomal dominant 38"
    ],
    "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 EEF1A2 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"
    }
  ]
}