{
  "id": 10588,
  "label": "autosomal recessive humeroradial synostosis",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0009356",
  "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)."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 7611,
      "label": "autosomal recessive disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        2905
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0050737",
          "EFO:1000017",
          "ICD9:758.5",
          "MEDGEN:539209",
          "SCTID:85995004",
          "UMLS:C0265388"
        ],
        "synonyms": [
          "autosomal recessive disease or disorder",
          "autosomal recessive hereditary disease",
          "autosomal recessive hereditary disorder",
          "autosomal recessive inherited disease",
          "autosomal recessive inherited disorder",
          "disease or disorder, autosomal recessive",
          "disease, autosomal recessive",
          "recessive hereditary disorder (autosomal)"
        ],
        "definition": "Autosomal recessive form of disease."
      },
      "child_count": 219,
      "reference_id": "MONDO:0006025"
    },
    {
      "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": 7611,
      "label": "autosomal recessive disease"
    },
    {
      "id": 9088,
      "label": "humeroradial synostosis"
    }
  ]
}