{
  "id": 11013,
  "label": "osteogenesis imperfecta type 3",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0009804",
  "properties": {
    "xrefs": [
      "DOID:0110339",
      "GARD:0008695",
      "MEDGEN:78664",
      "MESH:C536044",
      "NCIT:C99002",
      "OMIM:259420",
      "Orphanet:216812",
      "SCTID:385483009",
      "UMLS:C0268362",
      "icd11.foundation:629873920"
    ],
    "synonyms": [
      "OI type 3",
      "OI3",
      "osteogenesis imperfecta type 3",
      "osteogenesis imperfecta type III",
      "progressive deforming osteogenesis imperfecta",
      "severe osteogenesis imperfecta",
      "OI type III",
      "OI, type 3",
      "Oi3",
      "osteogenesis imperfecta, progressively deforming with normal sclerae",
      "osteogenesis imperfecta, progressively deforming, with normal sclerae",
      "osteogenesis imperfecta, type 3",
      "osteogenesis imperfecta, type III",
      "progressively deforming OI"
    ],
    "categories": [
      {
        "ref": "MONDO:0002081",
        "name": "musculoskeletal system disorder"
      }
    ],
    "definition": "Osteogenesis imperfecta type III is a severe type of osteogenesis imperfecta (OI), a genetic disorder characterized by increased bone fragility, low bone mass and susceptibility to bone fractures. The main signs of type III include very short stature, a triangular face, severe scoliosis, grayish sclera, and dentinogenesis imperfecta (DI)."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 24803,
      "label": "osteogenesis imperfecta and a reduction of bone mineral density.",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        18933
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0026427",
          "HP:0004349"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          }
        ],
        "definition": "A skeletal dysplasia characterized by osteogenesis imperfecta and decreased bone density."
      },
      "child_count": 34,
      "reference_id": "MONDO:0800064"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 24803,
      "label": "osteogenesis imperfecta and a reduction of bone mineral density."
    }
  ]
}