{
  "id": 11766,
  "label": "X-linked dominant hypophosphatemic rickets",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0010619",
  "properties": {
    "xrefs": [
      "DOID:0050445",
      "GARD:0012943",
      "MEDGEN:196551",
      "NANDO:1200779",
      "NCIT:C85234",
      "OMIM:307800",
      "Orphanet:89936",
      "SCTID:82236004",
      "UMLS:C0733682"
    ],
    "synonyms": [
      "X-linked hypophosphatemia",
      "X-linked hypophosphatemic rickets",
      "X-linked dominant hypophosphatemic rickets",
      "X-linked hereditary hypophosphatemic rickets",
      "XLH",
      "hereditary hypophosphatemic rickets, X-linked",
      "hypophosphatemic rickets, X-linked",
      "hypophosphatemic rickets, X-linked dominant, X-linked dominant",
      "rickets, vitamin D-resistant",
      "vitamin D-resistant rickets, X-linked",
      "HPDR",
      "HYP",
      "XLHR",
      "hypophophatemia, X-linked",
      "hypophophatemic vitamin D-resistant rickets",
      "hypophosphatemia, X-linked",
      "hypophosphatemic rickets, X-linked dominant",
      "hypophosphatemic vitamin D-resistant rickets"
    ],
    "categories": [
      {
        "ref": "MONDO:0002081",
        "name": "musculoskeletal system disorder"
      }
    ],
    "definition": "X-linked hypophosphatemia (XLH) is a hereditary renal phosphate-wasting disorder characterized by hypophosphatemia, rickets and/or osteomalacia, and diminished growth."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 20039,
      "label": "X-linked dominant disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        2902
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0080009",
          "MEDGEN:1798084",
          "UMLS:C5566661"
        ],
        "definition": "X-linked dominant form of disease."
      },
      "child_count": 1,
      "reference_id": "MONDO:0020604"
    },
    {
      "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": 20039,
      "label": "X-linked dominant disease"
    },
    {
      "id": 20126,
      "label": "X-linked hypophosphatemic rickets"
    },
    {
      "id": 24807,
      "label": "abnormal mineralization disorder"
    }
  ]
}