{
  "id": 9993,
  "label": "congenital isolated adrenocorticotropic hormone deficiency",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0008720",
  "properties": {
    "xrefs": [
      "DOID:0080150",
      "EFO:1001979",
      "GARD:0005727",
      "HP:0011748",
      "ICD9:255.41",
      "MEDGEN:137968",
      "MESH:C535668",
      "OMIM:201400",
      "Orphanet:199296",
      "SCTID:237692001",
      "UMLS:C0342388"
    ],
    "synonyms": [
      "adrenocorticotropic hormone deficiency",
      "congenital isolated adrenocorticotropic hormone deficiency (disease)",
      "ACTH deficiency, isolated",
      "IAD",
      "congenital isolated ACTH deficiency",
      "isolated ACTH deficiency",
      "isolated adrenocorticotropic hormone deficiency"
    ],
    "categories": [
      {
        "ref": "MONDO:0005039",
        "name": "reproductive system disorder"
      },
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      },
      {
        "ref": "MONDO:0005151",
        "name": "endocrine system disorder"
      }
    ],
    "definition": "A hypopituitarrium that is characterized by a decreased or absent production of adrenocorticotropic hormone by the pituitary gland."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "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"
    },
    {
      "id": 17048,
      "label": "isolated congenital hypogonadotropic hypogonadism",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        16526
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0020643",
          "MEDGEN:1842176",
          "Orphanet:238666",
          "UMLS:C5679849"
        ],
        "synonyms": [
          "nonsyndromic congenital hypogonadotropic hypogonadism"
        ],
        "categories": [
          {
            "ref": "MONDO:0005039",
            "name": "reproductive system disorder"
          },
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ],
        "definition": "A congenital hypogonadotropic hypogonadism that is not part of a larger syndrome."
      },
      "child_count": 1,
      "reference_id": "MONDO:0016553"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 14137,
      "label": "combined pituitary hormone deficiencies, genetic form"
    },
    {
      "id": 17048,
      "label": "isolated congenital hypogonadotropic hypogonadism"
    }
  ]
}