{
  "id": 8796,
  "label": "Crouzon syndrome",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0007405",
  "properties": {
    "xrefs": [
      "DOID:2339",
      "GARD:0006206",
      "MEDGEN:1162",
      "MESH:D003394",
      "NANDO:1200666",
      "NANDO:2200845",
      "NCIT:C84653",
      "NORD:1018",
      "OMIM:123500",
      "Orphanet:207",
      "SCTID:28861008",
      "UMLS:C0010273",
      "icd11.foundation:1535725821"
    ],
    "synonyms": [
      "Crouzon craniofacial dysostosis",
      "Crouzon syndrome",
      "craniofacial dysostosis",
      "Cfd1",
      "Crouzon disease",
      "craniofacial dysostosis type 1",
      "craniofacial dysostosis, type 1"
    ],
    "categories": [
      {
        "ref": "MONDO:0002081",
        "name": "musculoskeletal system disorder"
      },
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      }
    ],
    "definition": "Crouzon disease is characterized by craniosynostosis and facial hypoplasia."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 2,
  "parents": [
    {
      "id": 16201,
      "label": "syndromic craniosynostosis",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4370,
        16310,
        18360
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0019911",
          "MEDGEN:1842203",
          "Orphanet:139393",
          "UMLS:C5680624"
        ],
        "synonyms": [
          "syndrome associated with craniosynostosis",
          "syndromic craniosynostosis"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          }
        ],
        "definition": "A craniosynostosis that is part of a larger syndrome."
      },
      "child_count": 120,
      "reference_id": "MONDO:0015338"
    }
  ],
  "children": [
    {
      "id": 20836,
      "label": "cote katsantoni syndrome",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        8796
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0001554",
          "MEDGEN:419356",
          "MESH:C536449",
          "UMLS:C2931195"
        ],
        "synonyms": [
          "ectodermal dysplasia osteosclerosis"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0022311"
    },
    {
      "id": 20885,
      "label": "Bazopoulou Kyrkanidou syndrome",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        8796
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0000839",
          "MEDGEN:444091",
          "MESH:C537664",
          "UMLS:C2931580"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0022552"
    }
  ],
  "roots": [
    {
      "id": 16201,
      "label": "syndromic craniosynostosis"
    }
  ]
}