{
  "id": 11568,
  "label": "intellectual disability, X-linked syndromic, Turner type",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0010407",
  "properties": {
    "xrefs": [
      "DOID:0060811",
      "DOID:0060829",
      "GARD:0000081",
      "MEDGEN:394425",
      "MESH:C563154",
      "MESH:C567476",
      "OMIM:300612",
      "OMIM:300706",
      "OMIM:309590",
      "Orphanet:3056",
      "Orphanet:85328",
      "SCTID:725912001",
      "UMLS:C2678046"
    ],
    "synonyms": [
      "Brooks Wisniewski Brown syndrome",
      "Brooks-Wisniewski-Brown Syndrome",
      "Brooks-Wisniewski-Brown syndrome",
      "MRXST",
      "X-linked intellectual disability, Turner type",
      "intellectual disability, X-linked syndromic, Turner type",
      "mental retardation and macrocephaly syndrome",
      "mental retardation, X-linked, syndromic, Turner type",
      "Juberg-Marsidi Syndrome",
      "X-linked mental retardation Brooks type",
      "mental retardation, X-Linked, with growth retardation, deafness, and microgenitalism",
      "mental retardation, X-linked, syndromic, Brooks-Wisniewski-Brown Type",
      "mental retardation, X-linked, syndromic, Brooks-Wisniewski-Brown type"
    ],
    "categories": [
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      },
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "An X-linked syndromic intellectual disability characterized by moderate to severe intellectual deficit in boys and moderate intellectual deficit in girls. It has been described in 14 members from four generations of one family. Macrocephaly was reported and holoprosencephaly may also be present (two family members). The mode of transmission is X-linked semi-dominant."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 19742,
      "label": "X-linked syndromic intellectual disability",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        2961,
        24021
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0060309",
          "OMIMPS:309510",
          "Orphanet:98464"
        ],
        "synonyms": [
          "X-linked syndromic intellectual disability",
          "intellectual disability, X-linked syndromic",
          "mental retardation, X-linked syndromic",
          "syndromic X-linked intellectual disability",
          "syndromic intellectual disability, X-linked"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A syndromic intellectual disability with an X-linked mode of inheritance."
      },
      "child_count": 162,
      "reference_id": "MONDO:0020119"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 19742,
      "label": "X-linked syndromic intellectual disability"
    }
  ]
}