{
  "id": 13584,
  "label": "osteogenesis imperfecta type 7",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0012536",
  "properties": {
    "xrefs": [
      "DOID:0110337",
      "GARD:0008701",
      "MEDGEN:343981",
      "OMIM:610682",
      "SCTID:254111008",
      "UMLS:C1853162"
    ],
    "synonyms": [
      "CRTAP osteogenesis imperfecta",
      "OI7",
      "osteogenesis imperfecta caused by mutation in CRTAP",
      "osteogenesis imperfecta type 7",
      "OI type 7",
      "OI type VII",
      "OI, type 7",
      "osteogenesis imperfecta, type 7",
      "osteogenesis imperfecta, type IIb",
      "osteogenesis imperfecta, type IIb, formerly",
      "osteogenesis imperfecta, type VII"
    ],
    "categories": [
      {
        "ref": "MONDO:0002081",
        "name": "musculoskeletal system disorder"
      }
    ],
    "definition": "Any osteogenesis imperfecta in which the cause of the disease is a mutation in the CRTAP gene."
  },
  "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."
    }
  ]
}