{
  "id": 9113,
  "label": "autosomal dominant osteosclerosis, Worth type",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0007764",
  "properties": {
    "xrefs": [
      "DOID:0080037",
      "GARD:0000390",
      "MEDGEN:140932",
      "OMIM:144750",
      "OMIM:607636",
      "Orphanet:2790",
      "SCTID:254131007",
      "UMLS:C0432273",
      "icd11.foundation:1038854228"
    ],
    "synonyms": [
      "Ostéosclérose autosomique dominante type Worth",
      "Worth syndrome",
      "Worth's syndrome",
      "endosteal hyperostosis, Worth type",
      "hyperostosis, endosteal",
      "VBCH2",
      "Van Buchem disease type 2",
      "Van Buchem disease, type 2",
      "endosteal hyperostosis, autosomal dominant",
      "hyperostosis corticalis generalisata, benign form of Worth with torus palatinus",
      "hyperostosis corticalis generalisata, benign form of Worth, with torus palatinus",
      "osteosclerosis of the skull and enlarged mandible",
      "osteosclerosis, autosomal dominant",
      "osteosclerosis, autosomal dominant, Worth type"
    ],
    "categories": [
      {
        "ref": "MONDO:0002081",
        "name": "musculoskeletal system disorder"
      }
    ],
    "definition": "A sclerozing bone disorder characterized by generalized skeletal densification, particularly of the cranial vault and tubular long bones, which is not associated to an increased risk of fracture."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 4308,
      "label": "hyperostosis",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        3151
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:205",
          "ICD10CM:M89.3",
          "ICD9:733.99",
          "MEDGEN:9366",
          "MESH:D015576",
          "NCIT:C34712",
          "SCTID:203514008",
          "UMLS:C0020492"
        ],
        "synonyms": [
          "bone hypertrophy",
          "hypertrophy of bone",
          "hypertrophy of bone (morphologic abnormality)"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          }
        ],
        "definition": "Excessive thickening of bone."
      },
      "child_count": 9,
      "reference_id": "MONDO:0002185"
    },
    {
      "id": 18360,
      "label": "skeletal dysplasia",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5714,
        7061
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:98053",
          "Orphanet:364526",
          "UMLS:C0410528"
        ],
        "synonyms": [
          "Mendelian skeletal dysplasia",
          "primary bone dysplasia",
          "primary osteodysplasia",
          "primary skeletal dysplasia"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          }
        ],
        "definition": "Any Mendelian diseases that affects growth and development of the skeleton."
      },
      "child_count": 238,
      "reference_id": "MONDO:0018230"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 4308,
      "label": "hyperostosis"
    },
    {
      "id": 18360,
      "label": "skeletal dysplasia"
    }
  ]
}