{
  "id": 10282,
  "label": "craniodiaphyseal dysplasia",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0009031",
  "properties": {
    "xrefs": [
      "DOID:0080032",
      "GARD:0001567",
      "ICD9:756.59",
      "MEDGEN:96080",
      "MESH:C562940",
      "NANDO:2201368",
      "NCIT:C131429",
      "OMIM:218300",
      "Orphanet:1513",
      "SCTID:205506004",
      "UMLS:C0410539",
      "icd11.foundation:505073582"
    ],
    "synonyms": [
      "Lionitis",
      "craniodiaphyseal dysplasia",
      "CDD"
    ],
    "categories": [
      {
        "ref": "MONDO:0002081",
        "name": "musculoskeletal system disorder"
      }
    ],
    "definition": "Craniodiaphyseal dysplasia is a rare sclerotic bone disorder with a variable phenotypic expression with massive generalized hyperostosis and sclerosis, particularly of the skull and facial bones, that may lead to severe deformity."
  },
  "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": 16306,
      "label": "craniometaphyseal dysplasia",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        23099
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0080033",
          "GARD:0015013",
          "ICD9:756.89",
          "MEDGEN:82702",
          "NANDO:2201366",
          "NORD:1013",
          "OMIMPS:123000",
          "Orphanet:1522",
          "SCTID:36601008",
          "UMLS:C0265292",
          "icd11.foundation:305860050"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          }
        ],
        "definition": "Craniometaphyseal dysplasia (CMD) is a very rare genetic bone disease characterized by progressive diffuse hyperostosis of cranial bones causing facial dysmorphism and functional repercussions, and metaphyseal widening of long bones."
      },
      "child_count": 4,
      "reference_id": "MONDO:0015465"
    },
    {
      "id": 20383,
      "label": "disorder of development or morphogenesis",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        29380
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "ICD10CM:Q00-Q99",
          "MEDGEN:1843482",
          "UMLS:C0694457"
        ],
        "definition": "Any disease or disorder that disrupts the process development of an anatomical structure. Can be due to genetic or environmental causes. Typically happens during embryogenesis, but also includes post-embryonic development."
      },
      "child_count": 190,
      "reference_id": "MONDO:0021147"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 4308,
      "label": "hyperostosis"
    },
    {
      "id": 16306,
      "label": "craniometaphyseal dysplasia"
    },
    {
      "id": 20383,
      "label": "disorder of development or morphogenesis"
    }
  ]
}