{
  "id": 25785,
  "label": "osteogenesis imperfecta, type 23",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0957988",
  "properties": {
    "xrefs": [
      "GARD:0026901",
      "MEDGEN:1846121",
      "OMIM:620639",
      "UMLS:C5882757"
    ],
    "categories": [
      {
        "ref": "MONDO:0002081",
        "name": "musculoskeletal system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 18933,
      "label": "osteogenesis imperfecta",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        7171
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:12347",
          "GARD:0001017",
          "ICD10CM:Q78.0",
          "ICD9:756.51",
          "MEDGEN:45246",
          "MESH:D010013",
          "MedDRA:10031243",
          "NANDO:1200873",
          "NANDO:2201011",
          "NCIT:C26837",
          "NORD:1535",
          "OMIMPS:166200",
          "Orphanet:666",
          "SCTID:78314001",
          "UMLS:C0029434",
          "icd11.foundation:1219932551"
        ],
        "synonyms": [
          "Lobstein disease",
          "OI",
          "Osteopsathyrosis",
          "Porak and Durante disease",
          "brittle bone disease",
          "glass bone disease",
          "Vrolik disease"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          }
        ],
        "definition": "Osteogenesis imperfecta (OI) comprises a heterogeneous group of genetic disorders characterized by increased bone fragility, low bone mass, and susceptibility to bone fractures with variable severity."
      },
      "child_count": 10,
      "reference_id": "MONDO:0019019"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 18933,
      "label": "osteogenesis imperfecta"
    }
  ]
}