{
  "id": 14539,
  "label": "intellectual disability, autosomal dominant 6",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0013509",
  "properties": {
    "xrefs": [
      "DOID:0070036",
      "GARD:0012851",
      "MEDGEN:462761",
      "OMIM:613970",
      "Orphanet:589547",
      "UMLS:C3151411"
    ],
    "synonyms": [
      "GRIN2B encephalopathy",
      "GRIN2B-related neurodevelopmental disorder",
      "GRIN2B autosomal dominant non-syndromic intellectual disability",
      "GRIN2B-related developmental delay, intellectual disability and autism spectrum disorder",
      "MRD6",
      "autosomal dominant non-syndromic intellectual disability caused by mutation in GRIN2B",
      "intellectual developmental disorder, autosomal dominant 6, with or without seizures",
      "intellectual disability, autosomal dominant 6",
      "intellectual disability, autosomal dominant type 6",
      "mental retardation, autosomal dominant type 6",
      "mental retardation, autosomal dominant 6",
      "mental retardation, autosomal dominant 6, with or without seizures"
    ],
    "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 GRIN2B 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": 24724,
      "label": "GRIN2B-related complex neurodevelopmental disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        29312
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0028024"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A complex neurodevelopmental disorder caused by a variation in the GRIN2B gene"
      },
      "child_count": 2,
      "reference_id": "MONDO:0700350"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 23914,
      "label": "intellectual disability, autosomal dominant"
    },
    {
      "id": 24724,
      "label": "GRIN2B-related complex neurodevelopmental disorder"
    }
  ]
}