{
  "id": 17048,
  "label": "isolated congenital hypogonadotropic hypogonadism",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0016553",
  "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."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 1,
  "parents": [
    {
      "id": 16526,
      "label": "congenital hypogonadotropic hypogonadism",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        18569,
        19562
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0020135",
          "MEDGEN:859097",
          "NANDO:1200383",
          "NCIT:C120162",
          "Orphanet:174590",
          "SCTID:722944006",
          "UMLS:C3899503",
          "icd11.foundation:1752075408"
        ],
        "categories": [
          {
            "ref": "MONDO:0005039",
            "name": "reproductive system disorder"
          },
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ],
        "definition": "Congenital hypogonadotropic hypogonadism (CHH) is a rare disorder of sexual maturation characterized by gonadotropin (Gn) deficiency with low sex steroid levels associated with low levels of follicle stimulating hormone (FSH) and luteinizing hormone (LH)."
      },
      "child_count": 50,
      "reference_id": "MONDO:0015770"
    }
  ],
  "children": [
    {
      "id": 9993,
      "label": "congenital isolated adrenocorticotropic hormone deficiency",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        14137,
        17048
      ],
      "type_id": 0,
      "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."
      },
      "child_count": 0,
      "reference_id": "MONDO:0008720"
    }
  ],
  "roots": [
    {
      "id": 16526,
      "label": "congenital hypogonadotropic hypogonadism"
    }
  ]
}