{
  "id": 17775,
  "label": "femoral agenesis/hypoplasia, bilateral",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0017485",
  "properties": {
    "xrefs": [
      "Orphanet:295067"
    ],
    "synonyms": [
      "femoral intercalary meromelia, bilateral"
    ],
    "categories": [
      {
        "ref": "MONDO:0002081",
        "name": "musculoskeletal system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 16670,
      "label": "femoral agenesis/hypoplasia",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        18362,
        19479
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0001503",
          "ICD9:755.34",
          "MEDGEN:87499",
          "Orphanet:1987",
          "SCTID:93255008",
          "UMLS:C0345375",
          "icd11.foundation:662157487"
        ],
        "synonyms": [
          "congenital short femur",
          "femoral intercalary meromelia"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          }
        ],
        "definition": "Congenital short femur is a rare malformation of variable severity ranging from mild hypoplasia to complete absence of the femur."
      },
      "child_count": 4,
      "reference_id": "MONDO:0016032"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 16670,
      "label": "femoral agenesis/hypoplasia"
    }
  ]
}