{
  "id": 8613,
  "label": "Boomerang dysplasia",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0007208",
  "properties": {
    "xrefs": [
      "DOID:0050680",
      "GARD:0000933",
      "ICD9:756.9",
      "MEDGEN:96579",
      "MESH:C536573",
      "OMIM:112310",
      "Orphanet:1263",
      "SCTID:254054000",
      "UMLS:C0432201",
      "icd11.foundation:423736259"
    ],
    "synonyms": [
      "Boomerang dysplasia",
      "Boomerang-like skeletal dysplasia",
      "dwarfism with short, bowed, rigid limbs and characteristic facies"
    ],
    "categories": [
      {
        "ref": "MONDO:0002081",
        "name": "musculoskeletal system disorder"
      }
    ],
    "definition": "A rare lethal skeletal dysplasia characterized by severe short-limbed dwarfism, dislocated joints, club feet, distinctive facies and diagnostic x-ray findings of underossified and dysplastic long tubular bones, with a boomerang-like bowing."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 7171,
      "label": "osteochondrodysplasia",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        7153,
        18360
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:2256",
          "EFO:0005571",
          "ICD9:756.4",
          "MEDGEN:10495",
          "MESH:D010009",
          "NCIT:C84978",
          "SCTID:105985007",
          "UMLS:C0029422"
        ],
        "synonyms": [
          "skeletal dysplasia",
          "congenital skeletal dysplasia",
          "osteochondrodysplasia",
          "cartilage development disorder",
          "congenital anomaly of cartilage"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          }
        ],
        "definition": "A term referring to disorders characterized by abnormalities in the development of bones and cartilage."
      },
      "child_count": 100,
      "reference_id": "MONDO:0005516"
    },
    {
      "id": 29336,
      "label": "FLNB-associated autosomal dominant filamin related bone disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        2903,
        19470
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0028175"
        ],
        "synonyms": [
          "FLNB-associated autosomal dominant filamin related bone disorder"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          }
        ],
        "definition": "Any autosomal dominant filamin related bone disorder in which the cause of the disease is a variation in FLNB gene."
      },
      "child_count": 8,
      "reference_id": "MONDO:1060173"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 7171,
      "label": "osteochondrodysplasia"
    },
    {
      "id": 29336,
      "label": "FLNB-associated autosomal dominant filamin related bone disorder"
    }
  ]
}