{
  "id": 11735,
  "label": "diabetes insipidus, nephrogenic, X-linked",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0010581",
  "properties": {
    "xrefs": [
      "DOID:0081060",
      "GARD:0015289",
      "MEDGEN:288785",
      "OMIM:304800",
      "UMLS:C1563705"
    ],
    "synonyms": [
      "diabetes insipidus, nephrogenic, 1, X-linked recessive",
      "diabetes insipidus, nephrogenic, X-linked",
      "Ndi",
      "diabetes insipidus, nephrogenic, type 1"
    ],
    "categories": [
      {
        "ref": "MONDO:0002118",
        "name": "urinary system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 2902,
      "label": "X-linked disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5714
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0050735",
          "ICD9:799.89",
          "MEDGEN:222910",
          "MESH:D040181",
          "NCIT:C85865",
          "SCTID:128430005",
          "UMLS:C1138434"
        ],
        "synonyms": [
          "X-linked disease or disorder",
          "X-linked hereditary disease",
          "X-linked hereditary disorder",
          "X-linked inherited disease",
          "X-linked inherited disorder",
          "disease or disorder, X-linked",
          "disease, X-linked",
          "X linked genetic diseases",
          "X-linked genetic disease",
          "X-linked genetic diseases",
          "disease, X-linked genetic",
          "diseases, X-linked genetic",
          "genetic disease, X-linked",
          "genetic diseases, X chromosome linked",
          "genetic diseases, X linked",
          "genetic diseases, X-chromosome linked"
        ],
        "definition": "X-linked form of disease."
      },
      "child_count": 50,
      "reference_id": "MONDO:0000425"
    },
    {
      "id": 16914,
      "label": "nephrogenic diabetes insipidus",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        3571,
        6550,
        16626
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:12387",
          "GARD:0007178",
          "ICD10CM:N25.1",
          "ICD9:588.1",
          "MEDGEN:57876",
          "MESH:D018500",
          "MedDRA:10029147",
          "NANDO:1200742",
          "NANDO:2200326",
          "NCIT:C84919",
          "NORD:1497",
          "Orphanet:223",
          "SCTID:111395007",
          "UMLS:C0162283",
          "icd11.foundation:1417669099"
        ],
        "synonyms": [
          "ADH resistant diabetes insipidus",
          "diabetes insipidus nephrogenic",
          "diabetes insipidus nephrogenic X-linked",
          "diabetes insipidus nephrogenic type 1"
        ],
        "categories": [
          {
            "ref": "MONDO:0002118",
            "name": "urinary system disorder"
          }
        ],
        "definition": "Nephrogenic diabetes insipidus (NDI) is characterized by polyuria with polydipsia, recurrent bouts of fever, constipation, and acute hypernatremic dehydration after birth that may cause neurological sequelae. Polyuria may exceed 10 liters in children."
      },
      "child_count": 6,
      "reference_id": "MONDO:0016383"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 2902,
      "label": "X-linked disease"
    },
    {
      "id": 16914,
      "label": "nephrogenic diabetes insipidus"
    }
  ]
}