{
  "id": 6550,
  "label": "diabetes insipidus",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0004782",
  "properties": {
    "xrefs": [
      "DOID:9409",
      "ICD10CM:E23.2",
      "ICD9:253.5",
      "MEDGEN:8349",
      "MESH:D003919",
      "NANDO:2100117",
      "NCIT:C43263",
      "SCTID:15771004",
      "UMLS:C0011848"
    ],
    "categories": [
      {
        "ref": "MONDO:0002118",
        "name": "urinary system disorder"
      }
    ],
    "definition": "A disorder characterized by excretion of large amounts of urine, accompanied by excessive thirst. Causes include deficiency of antidiuretic hormone or failure of the kidneys to respond to antidiuretic hormone. It may also be drug-related."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 4,
  "parents": [
    {
      "id": 6948,
      "label": "kidney disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4253
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:557",
          "EFO:0003086",
          "ICD9:583.81",
          "MEDGEN:9635",
          "MESH:D007674",
          "NCIT:C3149",
          "SCTID:90708001",
          "UMLS:C0022658"
        ],
        "synonyms": [
          "disease of kidney",
          "disease or disorder of kidney",
          "disorder of kidney",
          "kidney disease",
          "kidney disease or disorder",
          "kidney disorder",
          "renal disease",
          "renal disorder",
          "nephropathy"
        ],
        "categories": [
          {
            "ref": "MONDO:0002118",
            "name": "urinary system disorder"
          }
        ],
        "definition": "A disease involving the kidney."
      },
      "child_count": 57,
      "reference_id": "MONDO:0005240"
    }
  ],
  "children": [
    {
      "id": 8840,
      "label": "neurohypophyseal diabetes insipidus",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        2903,
        5314,
        6550,
        16543,
        23932,
        24270
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:12388",
          "GARD:0016629",
          "MEDGEN:574999",
          "NANDO:2201050",
          "NCIT:C84933",
          "OMIM:125700",
          "Orphanet:30925",
          "SCTID:45369008",
          "UMLS:C0342394",
          "icd11.foundation:97299603"
        ],
        "synonyms": [
          "ADH deficiency",
          "AVP deficiency",
          "Arginine vasopressin deficiency",
          "antidiuretic hormone deficiency",
          "diabetes insipidus of pituitary gland",
          "hereditary CDI",
          "hereditary neurogenic diabetes insipidus",
          "pituitary gland diabetes insipidus",
          "vasopressin deficiency",
          "diabetes insipidus, cranial type",
          "diabetes insipidus, neurohypophyseal",
          "diabetes insipidus, primary central",
          "hereditary central diabetes insipidus",
          "neurogenic diabetes insipidus"
        ],
        "categories": [
          {
            "ref": "MONDO:0002118",
            "name": "urinary system disorder"
          },
          {
            "ref": "MONDO:0005039",
            "name": "reproductive system disorder"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          },
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ],
        "definition": "Hereditary central diabetes insipidus is a rare genetic subtype of central diabetes insipidus (CDI) characterized by polyuria and polydipsia due to a deficiency in vasopressin (AVP) synthesis."
      },
      "child_count": 0,
      "reference_id": "MONDO:0007450"
    },
    {
      "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"
    },
    {
      "id": 21086,
      "label": "dipsogenic diabetes insipidus",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        6550,
        23013
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0081058",
          "MEDGEN:82829",
          "MESH:C548013",
          "NCIT:C129735",
          "SCTID:82800008",
          "UMLS:C0268813"
        ],
        "synonyms": [
          "primary polydipsia",
          "Dipsogenic diabetes insipidus",
          "dipsogenic diabetes insipidus"
        ],
        "categories": [
          {
            "ref": "MONDO:0002118",
            "name": "urinary system disorder"
          }
        ],
        "definition": "Diabetes insipidus caused by excessive intake of water due to psychological factors or damage to the thirst-regulating mechanism."
      },
      "child_count": 0,
      "reference_id": "MONDO:0022993"
    },
    {
      "id": 21190,
      "label": "gestational diabetes insipidus",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        6550
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0081057",
          "MEDGEN:444359",
          "MESH:C548014",
          "UMLS:C2932666"
        ],
        "synonyms": [
          "Gestagenic diabetes insipidus",
          "diabetes insipidus gestational"
        ],
        "categories": [
          {
            "ref": "MONDO:0002118",
            "name": "urinary system disorder"
          }
        ],
        "definition": "A form of diabetes insipidus that manifests during pregnancy (or in some cases, after pregnancy). It is characterized by theappearance of a polyuric-polydipsic syndrome that resultsin fluid intake ranging from 3 to 20 L/day. It is also charac-terized by excretion of abnormally high volumes of dilutedurine. This polyuria is insipid, i.e., the urine concentrationof dissolved substances is very low."
      },
      "child_count": 0,
      "reference_id": "MONDO:0023227"
    }
  ],
  "roots": [
    {
      "id": 6948,
      "label": "kidney disorder"
    }
  ]
}