{
  "id": 13536,
  "label": "alopecia-intellectual disability syndrome 2",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0012487",
  "properties": {
    "xrefs": [
      "DOID:0080629",
      "GARD:0004291",
      "MEDGEN:372142",
      "MESH:C563668",
      "OMIM:610422",
      "UMLS:C1835852"
    ],
    "synonyms": [
      "alopecia-intellectual disability syndrome 2",
      "alopecia-mental retardation syndrome 2",
      "AMR syndrome 2",
      "APMR2",
      "alopecia intellectual disability syndrome 2",
      "alopecia with mild to moderate intellectual deficit"
    ],
    "categories": [
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 10029,
      "label": "alopecia - intellectual disability syndrome",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4370,
        5714
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0080627",
          "GARD:0000612",
          "MEDGEN:444019",
          "OMIMPS:203650",
          "Orphanet:2850",
          "SCTID:716191002",
          "UMLS:C2931280"
        ],
        "synonyms": [
          "Perniola-Krajewska-Carnevale syndrome",
          "alopecia-intellectual disability syndrome",
          "AMR syndrome 1",
          "Amr syndrome",
          "alopecia intellectual disbility syndrome 1",
          "alopecia with severe intellectual deficit"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          }
        ],
        "definition": "An extremely rare syndrome described in less than 20 families to date and characterized by total or partial alopecia associated with intellectual deficit. The syndrome can be associated with other anomalies such as seizures, sensorineural hearing loss, delayed psychomotor development, and/or hypertonia."
      },
      "child_count": 8,
      "reference_id": "MONDO:0008756"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 10029,
      "label": "alopecia - intellectual disability syndrome"
    }
  ]
}