{
  "id": 23748,
  "label": "intellectual developmental disorder with speech delay, dysmorphic facies, and t-cell abnormalities",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0060763",
  "properties": {
    "xrefs": [
      "GARD:0027142",
      "MEDGEN:1648327",
      "OMIM:618092",
      "Orphanet:662829",
      "UMLS:C4748152"
    ],
    "synonyms": [
      "BCL11B-related disorder",
      "BCL11B-related BAFopathy",
      "intellectual developmental disorder with dysmorphic facies, speech delay, and t-cell abnormalities",
      "IDDSFTA",
      "INTELLECTUAL developmental disorder with speech delay, DYSMORPHIC facies, and T-cell abnormalities"
    ],
    "categories": [
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      },
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "Any BAFopathy in which the cause of the disease is a mutation in the BCL11B gene."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 24323,
      "label": "autosomal dominant syndromic intellectual disability",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        2961,
        23914
      ],
      "type_id": 0,
      "properties": {
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Autosomal dominant form of syndromic intellectual disability."
      },
      "child_count": 68,
      "reference_id": "MONDO:0100601"
    },
    {
      "id": 24515,
      "label": "BAFopathy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5714
      ],
      "type_id": 0,
      "properties": {
        "definition": "Disorder caused by mutations in the various subunits composing the BAF complex."
      },
      "child_count": 15,
      "reference_id": "MONDO:0700120"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 24323,
      "label": "autosomal dominant syndromic intellectual disability"
    },
    {
      "id": 24515,
      "label": "BAFopathy"
    }
  ]
}