{
  "id": 20885,
  "label": "Bazopoulou Kyrkanidou syndrome",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0022552",
  "properties": {
    "xrefs": [
      "GARD:0000839",
      "MEDGEN:444091",
      "MESH:C537664",
      "UMLS:C2931580"
    ],
    "categories": [
      {
        "ref": "MONDO:0002081",
        "name": "musculoskeletal system disorder"
      },
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 8796,
      "label": "Crouzon syndrome",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        16201
      ],
      "type_id": 0,
      "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."
      },
      "child_count": 2,
      "reference_id": "MONDO:0007405"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 8796,
      "label": "Crouzon syndrome"
    }
  ]
}