{
  "id": 19574,
  "label": "acquired central diabetes insipidus",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0019846",
  "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."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 16543,
      "label": "central diabetes insipidus",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        16072,
        23822
      ],
      "type_id": 0,
      "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)."
      },
      "child_count": 4,
      "reference_id": "MONDO:0015790"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 16543,
      "label": "central diabetes insipidus"
    }
  ]
}