{
  "id": 11524,
  "label": "hypophosphatemic rickets, X-linked recessive",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0010358",
  "properties": {
    "xrefs": [
      "DOID:0080353",
      "GARD:0015011",
      "MEDGEN:335115",
      "OMIM:300554",
      "UMLS:C1845168"
    ],
    "synonyms": [
      "CLCN5 X-linked hypophosphatemic rickets",
      "X-linked hypophosphatemic rickets caused by mutation in CLCN5",
      "hypophosphatemic rickets, X-linked recessive"
    ],
    "categories": [
      {
        "ref": "MONDO:0002081",
        "name": "musculoskeletal system disorder"
      }
    ],
    "definition": "Any X-linked hypophosphatemic rickets in which the cause of the disease is a mutation in the CLCN5 gene."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 20040,
      "label": "X-linked recessive disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        2902
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0080012",
          "MEDGEN:1798083",
          "UMLS:C5566660"
        ],
        "definition": "X-linked recessive form of disease."
      },
      "child_count": 12,
      "reference_id": "MONDO:0020605"
    },
    {
      "id": 20126,
      "label": "X-linked hypophosphatemic rickets",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        2709,
        2902
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0025223",
          "MEDGEN:761927",
          "MESH:D053098",
          "NCIT:C123265",
          "UMLS:C3540852",
          "icd11.foundation:1169135980"
        ],
        "synonyms": [
          "X-linked hypophosphatemic rickets",
          "X-linked hypophosphatemic rickets (recessive or dominant)"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          }
        ]
      },
      "child_count": 4,
      "reference_id": "MONDO:0020720"
    },
    {
      "id": 24807,
      "label": "abnormal mineralization disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        18360
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0026430"
        ],
        "synonyms": [
          "disorder of bone mineralization",
          "osteomalacia"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          }
        ],
        "definition": "A skeletal dysplasia where osteoid becomes calcified."
      },
      "child_count": 18,
      "reference_id": "MONDO:0800096"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 20040,
      "label": "X-linked recessive disease"
    },
    {
      "id": 20126,
      "label": "X-linked hypophosphatemic rickets"
    },
    {
      "id": 24807,
      "label": "abnormal mineralization disorder"
    }
  ]
}