{
  "id": 22134,
  "label": "microcephaly 27, primary, autosomal dominant",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0030929",
  "properties": {
    "xrefs": [
      "DOID:0051038",
      "GARD:0016433",
      "MEDGEN:1783457",
      "OMIM:619180",
      "UMLS:C5543051"
    ],
    "synonyms": [
      "MCPH27",
      "microcephaly 27, primary, autosomal dominant"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 9314,
      "label": "autosomal dominant primary microcephaly",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        2903,
        4427,
        16088,
        16689,
        24226
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0061100",
          "DOID:14725",
          "GARD:0003605",
          "MEDGEN:66319",
          "MESH:C537323",
          "OMIM:156580",
          "Orphanet:2514",
          "UMLS:C0220693",
          "icd11.foundation:774437947"
        ],
        "synonyms": [
          "autosomal dominant primary microcephaly",
          "microcephaly (disease), autosomal dominant",
          "autosomal dominant microcephaly",
          "microcephaly autosomal dominant",
          "microcephaly with autosomal dominant inheritance",
          "microcephaly, autosomal dominant"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Autosomal dominant form of microcephaly (disease)."
      },
      "child_count": 15,
      "reference_id": "MONDO:0007988"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 9314,
      "label": "autosomal dominant primary microcephaly"
    }
  ]
}