{
  "id": 9938,
  "label": "autosomal dominant hypophosphatemic rickets",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0008660",
  "properties": {
    "xrefs": [
      "DOID:0050948",
      "GARD:0016781",
      "MEDGEN:83346",
      "MESH:C562791",
      "OMIM:193100",
      "Orphanet:89937",
      "SCTID:237889002",
      "UMLS:C0342642"
    ],
    "synonyms": [
      "ADHR",
      "autosomal dominant hereditary hypophosphatemic rickets",
      "autosomal dominant hypophosphatemia",
      "autosomal dominant hypophosphatemic rickets",
      "hereditary hypophosphatemic rickets, autosomal dominant",
      "hypophosphatemic rickets, autosomal dominant",
      "hypophosphatemia, autosomal dominant",
      "vitamin D-resistant rickets, autosomal dominant"
    ],
    "categories": [
      {
        "ref": "MONDO:0002081",
        "name": "musculoskeletal system disorder"
      }
    ],
    "definition": "Autosomal dominant hypophosphatemic rickets (ADHR) is a hereditary renal phosphate-wasting disorder characterized by hypophosphatemia, rickets and/or osteomalacia."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 2709,
      "label": "hereditary hypophosphatemic rickets",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5714,
        21333
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0006735",
          "MedDRA:10060873",
          "OMIMPS:193100",
          "Orphanet:437",
          "icd11.foundation:1010293846"
        ],
        "synonyms": [
          "hereditary hypophosphatemic rickets"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          }
        ],
        "definition": "Hypophosphatemic rickets is a group of genetic diseases characterized by hypophosphatemia, rickets, and normal serum levels of calcium."
      },
      "child_count": 8,
      "reference_id": "MONDO:0000044"
    },
    {
      "id": 2903,
      "label": "autosomal dominant disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        2905
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0050736",
          "ICD9:758.5",
          "MEDGEN:539206",
          "SCTID:11164009",
          "UMLS:C0265385"
        ],
        "synonyms": [
          "autosomal dominant disease or disorder",
          "autosomal dominant hereditary disorder",
          "autosomal dominant inherited disorder",
          "disease or disorder, autosomal dominant",
          "disease, autosomal dominant"
        ],
        "definition": "Autosomal dominant form of disease."
      },
      "child_count": 192,
      "reference_id": "MONDO:0000426"
    },
    {
      "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": 2709,
      "label": "hereditary hypophosphatemic rickets"
    },
    {
      "id": 2903,
      "label": "autosomal dominant disease"
    },
    {
      "id": 24807,
      "label": "abnormal mineralization disorder"
    }
  ]
}