{
  "id": 19394,
  "label": "panhypopituitarism",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0019591",
  "properties": {
    "xrefs": [
      "DOID:9410",
      "GARD:0015020",
      "ICD9:253.2",
      "MEDGEN:69171",
      "MedDRA:10033662",
      "NCIT:C110940",
      "Orphanet:90695",
      "SCTID:32390006",
      "UMLS:C0242343",
      "icd11.foundation:1576287890"
    ],
    "synonyms": [
      "complete hypopituitarism"
    ],
    "categories": [
      {
        "ref": "MONDO:0005039",
        "name": "reproductive system disorder"
      },
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      },
      {
        "ref": "MONDO:0005151",
        "name": "endocrine system disorder"
      }
    ],
    "definition": "Insufficient production of all the anterior pituitary hormones."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 2,
  "parents": [
    {
      "id": 14137,
      "label": "combined pituitary hormone deficiencies, genetic form",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4427,
        6876,
        16526,
        24270
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0010602",
          "MEDGEN:906592",
          "OMIMPS:613038",
          "Orphanet:95494",
          "SCTID:718182008",
          "UMLS:C4273747"
        ],
        "synonyms": [
          "familial congenital hypopituitarism",
          "genetic hypopituitarism",
          "multiple pituitary hormone deficiencies, genetic forms",
          "pituitary hormone deficiency, combined",
          "combined pituitary hormone deficiencies, genetic forms",
          "familial hypopituitarism"
        ],
        "categories": [
          {
            "ref": "MONDO:0005039",
            "name": "reproductive system disorder"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          },
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ],
        "definition": "Congenital hypopituitarism is characterized by multiple pituitary hormone deficiency, including somatotroph, thyrotroph, lactotroph, corticotroph or gonadotroph deficiencies, due to mutations of pituitary transcription factors involved in pituitary ontogenesis. Congenital hypopituitarism is rare compared with the high incidence of hypopituitarism induced by pituitary adenomas, transsphenoidal surgery or radiotherapy."
      },
      "child_count": 36,
      "reference_id": "MONDO:0013099"
    }
  ],
  "children": [
    {
      "id": 11081,
      "label": "pituitary hormone deficiency, combined, 2",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19394
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0061020",
          "GARD:0015222",
          "MEDGEN:209236",
          "MESH:C563172",
          "OMIM:262600",
          "UMLS:C0878683"
        ],
        "synonyms": [
          "PROP1 combined pituitary hormone deficiencies, genetic form",
          "combined pituitary hormone deficiencies, genetic form caused by mutation in PROP1",
          "pituitary hormone deficiency, combined, 2",
          "pituitary hormone deficiency, combined, type 2",
          "CPHD2",
          "Hanhart dwarfism",
          "ateliotic dwarfism with hypogonadism",
          "panhypopituitarism",
          "pituitary dwarfism 3"
        ],
        "categories": [
          {
            "ref": "MONDO:0005039",
            "name": "reproductive system disorder"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          },
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ],
        "definition": "Any combined pituitary hormone deficiencies, genetic form in which the cause of the disease is a mutation in the PROP1 gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0009878"
    },
    {
      "id": 11854,
      "label": "panhypopituitarism, X-linked",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19394
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0111779",
          "GARD:0006737",
          "MEDGEN:87439",
          "MESH:C538613",
          "OMIM:312000",
          "SCTID:237683004",
          "UMLS:C0342376"
        ],
        "synonyms": [
          "panhypopituitarism, X-linked",
          "PHPX",
          "panhypopituitarism X-linked",
          "pituitary dwarfism IV",
          "pituitary dwarfism IV (formerly)",
          "pituitary dwarfism IV, formerly"
        ],
        "categories": [
          {
            "ref": "MONDO:0005039",
            "name": "reproductive system disorder"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          },
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0010712"
    }
  ],
  "roots": [
    {
      "id": 14137,
      "label": "combined pituitary hormone deficiencies, genetic form"
    }
  ]
}