{
  "id": 9088,
  "label": "humeroradial synostosis",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0007737",
  "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."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 4,
  "parents": [
    {
      "id": 3632,
      "label": "synostosis",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        18362
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:11971",
          "GARD:0022939",
          "MEDGEN:11689",
          "MESH:D013580",
          "UMLS:C0039093"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          }
        ],
        "definition": "A disease characterized by abnormal union between adjacent bones or parts of a single bone formed by osseous material, such as ossified connecting cartilage or fibrous tissue."
      },
      "child_count": 11,
      "reference_id": "MONDO:0001411"
    },
    {
      "id": 5714,
      "label": "hereditary disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        29382
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:630",
          "EFO:0000508",
          "ICD9:799.89",
          "MEDGEN:5527",
          "MESH:D030342",
          "NCIT:C3101",
          "SCTID:32895009",
          "UMLS:C0019247"
        ],
        "synonyms": [
          "genetic condition",
          "genetic disease",
          "genetic disorder",
          "hereditary disease",
          "hereditary disease or disorder",
          "hereditary diseases",
          "inherited disease",
          "inherited genetic disease",
          "molecular disease",
          "Mendelian disease",
          "familial disorder",
          "inborn disorder"
        ],
        "definition": "A disease that is caused by genetic modifications where those modifications are inherited from a parent's genome."
      },
      "child_count": 1925,
      "reference_id": "MONDO:0003847"
    }
  ],
  "children": [
    {
      "id": 10588,
      "label": "autosomal recessive humeroradial synostosis",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        7611,
        9088
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0024661",
          "MEDGEN:1875232",
          "OMIM:236400",
          "UMLS:C5975703"
        ],
        "synonyms": [
          "autosomal recessive humeroradial synostosis (disease)",
          "humeroradial synostosis (disease), autosomal recessive",
          "humeroradial synostosis",
          "humeroradial/multiple synostosis syndrome"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          }
        ],
        "definition": "Autosomal recessive form of humeroradial synostosis (disease)."
      },
      "child_count": 0,
      "reference_id": "MONDO:0009356"
    },
    {
      "id": 10589,
      "label": "humeroradial synostosis with craniofacial anomalies",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        9088
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0024662",
          "MEDGEN:369834",
          "MESH:C566888",
          "OMIM:236410",
          "UMLS:C1968717"
        ],
        "synonyms": [
          "humeroradial synostosis with craniofacial anomalies"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0009357"
    },
    {
      "id": 17831,
      "label": "humero-radial synostosis, unilateral",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        9088
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "Orphanet:295209",
          "icd11.foundation:695744743"
        ],
        "synonyms": [
          "humero-radial fusion, unilateral"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0017550"
    },
    {
      "id": 17832,
      "label": "humero-radial synostosis, bilateral",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        9088
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "Orphanet:295211",
          "icd11.foundation:1424025632"
        ],
        "synonyms": [
          "humero-radial fusion, bilateral"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0017551"
    }
  ],
  "roots": [
    {
      "id": 3632,
      "label": "synostosis"
    },
    {
      "id": 5714,
      "label": "hereditary disease"
    }
  ]
}