{
  "id": 8840,
  "label": "neurohypophyseal diabetes insipidus",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0007450",
  "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."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "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": 5314,
      "label": "pituitary gland disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6772,
        6875,
        7209
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:53",
          "EFO:0009607",
          "ICD9:253.1",
          "ICD9:253.8",
          "ICD9:253.9",
          "MEDGEN:45934",
          "MESH:D010900",
          "NCIT:C26854",
          "SCTID:399244003",
          "UMLS:C0032002"
        ],
        "synonyms": [
          "disease of pituitary gland",
          "disease or disorder of pituitary gland",
          "disorder of pituitary gland",
          "pituitary gland disease",
          "pituitary gland disease or disorder",
          "pituitary gland disorder"
        ],
        "categories": [
          {
            "ref": "MONDO:0005039",
            "name": "reproductive system disorder"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          },
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ],
        "definition": "A disease involving the pituitary gland."
      },
      "child_count": 27,
      "reference_id": "MONDO:0003381"
    },
    {
      "id": 6550,
      "label": "diabetes insipidus",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6948
      ],
      "type_id": 0,
      "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."
      },
      "child_count": 4,
      "reference_id": "MONDO:0004782"
    },
    {
      "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"
    },
    {
      "id": 23932,
      "label": "inherited kidney disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5714,
        6948
      ],
      "type_id": 0,
      "properties": {
        "synonyms": [
          "genetic renal disease",
          "inherited kidney disease",
          "inherited renal disorder",
          "nephrogenetic disorder"
        ],
        "categories": [
          {
            "ref": "MONDO:0002118",
            "name": "urinary system disorder"
          }
        ],
        "definition": "A heterogeneous group of genetic conditions, with Mendelian (autosomal dominant, recessive, or X-linked) or chromosomal etiology that are characterized by abnormalities in the kidney or urinary system."
      },
      "child_count": 52,
      "reference_id": "MONDO:0100191"
    },
    {
      "id": 24270,
      "label": "hereditary neurological disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5714,
        6799
      ],
      "type_id": 0,
      "properties": {
        "synonyms": [
          "neurogenetic disease"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A heterogeneous group of genetic conditions with Mendelian (autosomal dominant, recessive, or X-linked) or chromosomal etiology characterized by abnormalities in the brain, spinal cord, nerves, or muscles."
      },
      "child_count": 528,
      "reference_id": "MONDO:0100545"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 2903,
      "label": "autosomal dominant disease"
    },
    {
      "id": 5314,
      "label": "pituitary gland disorder"
    },
    {
      "id": 6550,
      "label": "diabetes insipidus"
    },
    {
      "id": 16543,
      "label": "central diabetes insipidus"
    },
    {
      "id": 23932,
      "label": "inherited kidney disorder"
    },
    {
      "id": 24270,
      "label": "hereditary neurological disease"
    }
  ]
}