{
  "id": 8788,
  "label": "craniometaphyseal dysplasia, autosomal dominant",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0007397",
  "properties": {
    "xrefs": [
      "DOID:0080801",
      "GARD:0001581",
      "MEDGEN:338945",
      "MESH:C565145",
      "OMIM:123000",
      "UMLS:C1852502"
    ],
    "synonyms": [
      "craniometaphyseal dysplasia, autosomal dominant",
      "CMD",
      "CMDD",
      "CMDJ",
      "craniometaphyseal dysplasia Jackson type",
      "craniometaphyseal dysplasia, Jackson type"
    ],
    "categories": [
      {
        "ref": "MONDO:0002081",
        "name": "musculoskeletal system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "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"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 16306,
      "label": "craniometaphyseal dysplasia"
    }
  ]
}