{
  "id": 17832,
  "label": "humero-radial synostosis, bilateral",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0017551",
  "properties": {
    "xrefs": [
      "Orphanet:295211",
      "icd11.foundation:1424025632"
    ],
    "synonyms": [
      "humero-radial fusion, bilateral"
    ],
    "categories": [
      {
        "ref": "MONDO:0002081",
        "name": "musculoskeletal system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 9088,
      "label": "humeroradial synostosis",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        3632,
        5714
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0060467",
          "GARD:0002748",
          "HP:0003041",
          "ICD9:755.59",
          "MEDGEN:418931",
          "OMIM:143050",
          "Orphanet:3265",
          "SCTID:205329008",
          "UMLS:C2930865",
          "icd11.foundation:518723993"
        ],
        "synonyms": [
          "humero-radial fusion",
          "humeroradial synostosis",
          "humeroradial synostosis (disease)",
          "humero-radial synostosis"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          }
        ],
        "definition": "Humero-radial synostosis is a rare, genetic, congenital joint formation defect disorder characterized by uni- or bilateral fusion of the humerus and radius bones at the elbow level, with or without associated ulnar and carpal/metacarpal deficiency, leading to loss of elbow motion and, in many cases, functional arm incapacity. Bowing of radius may be additionally present."
      },
      "child_count": 8,
      "reference_id": "MONDO:0007737"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 9088,
      "label": "humeroradial synostosis"
    }
  ]
}