{
  "id": 16543,
  "label": "central diabetes insipidus",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0015790",
  "properties": {
    "xrefs": [
      "DOID:0081055",
      "GARD:0006015",
      "HP:0000863",
      "MEDGEN:146919",
      "MedDRA:10068587",
      "NANDO:1200375",
      "NANDO:2200324",
      "Orphanet:178029",
      "UMLS:C0687720",
      "icd11.foundation:1009553897"
    ],
    "synonyms": [
      "CDI",
      "neurogenic diabetes insipidus",
      "diabetes insipidus cranial type",
      "diabetes insipidus neurogenic",
      "diabetes insipidus neurohypophyseal"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      },
      {
        "ref": "MONDO:0005151",
        "name": "endocrine system disorder"
      }
    ],
    "definition": "Central diabetes insipidus (CDI) is a hypothalamus-pituitary disease characterized by polyuria and polydipsia due to a vasopressin (AVP) deficiency. It can be inherited or acquired (hereditary CDI and acquired CDI)."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 2,
  "parents": [
    {
      "id": 16072,
      "label": "pituitary deficiency",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6875
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0019801",
          "Orphanet:101957",
          "icd11.foundation:292840069"
        ],
        "categories": [
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ]
      },
      "child_count": 5,
      "reference_id": "MONDO:0015127"
    },
    {
      "id": 23822,
      "label": "neuroendocrine disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6799,
        6875
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:1843486",
          "UMLS:C0541403"
        ],
        "synonyms": [
          "neuroendocrine system disease"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          },
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ],
        "definition": "A disease or disorder that affects the neuroendocrine gland, any of the organized aggregations of cells that function as secretory or excretory organs and that release hormones in response to neural stimuli."
      },
      "child_count": 8,
      "reference_id": "MONDO:0100070"
    }
  ],
  "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": 19574,
      "label": "acquired central diabetes insipidus",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        16543
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0019291",
          "MEDGEN:1843437",
          "Orphanet:95626",
          "UMLS:C5680256",
          "icd11.foundation:1677009817"
        ],
        "synonyms": [
          "acquired CDI",
          "acquired central diabetes insipidus",
          "acquired neurogenic diabetes insipidus"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          },
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ],
        "definition": "Acquired central diabetes insipidus (acquired CDI) is a subtype of central diabetes insipidus (CDI), characterized by polyuria and polydipsia, due to an idiopathic or secondary decrease in vasopressin (AVP) production."
      },
      "child_count": 0,
      "reference_id": "MONDO:0019846"
    }
  ],
  "roots": [
    {
      "id": 16072,
      "label": "pituitary deficiency"
    },
    {
      "id": 23822,
      "label": "neuroendocrine disorder"
    }
  ]
}