{
  "id": 13363,
  "label": "familial scaphocephaly syndrome, McGillivray type",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0012307",
  "properties": {
    "xrefs": [
      "GARD:0003426",
      "MEDGEN:355365",
      "MESH:C566511",
      "OMIM:609579",
      "Orphanet:168624",
      "UMLS:C1865070",
      "icd11.foundation:512057922"
    ],
    "synonyms": [
      "scaphocephaly-macrocephaly-maxillary retrusion-intellectual disability syndrome",
      "scaphocephaly, maxillary retrusion, and intellectual disability",
      "scaphocephaly, maxillary retrusion, and mental retardation"
    ],
    "categories": [
      {
        "ref": "MONDO:0002081",
        "name": "musculoskeletal system disorder"
      },
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      }
    ],
    "definition": "Familial scaphocephaly syndrome, McGillivray type is a rare newly described craniosynostosis syndrome characterized by scaphocephaly, macrocephaly, severe maxillary retrusion, and mild intellectual disability."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 16468,
      "label": "familial scaphocephaly syndrome",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        16201
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0020113",
          "MEDGEN:797875",
          "MedDRA:10072229",
          "Orphanet:169163",
          "UMLS:C3267076"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          }
        ]
      },
      "child_count": 2,
      "reference_id": "MONDO:0015704"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 16468,
      "label": "familial scaphocephaly syndrome"
    }
  ]
}