{
  "id": 9139,
  "label": "hypogonadotropic hypogonadism 7 with or without anosmia",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0007794",
  "properties": {
    "xrefs": [
      "DOID:0090078",
      "GARD:0002897",
      "ICD9:253.4",
      "MEDGEN:87440",
      "MESH:C562785",
      "NANDO:1200382",
      "OMIM:146110",
      "SCTID:123953004",
      "UMLS:C0342384"
    ],
    "synonyms": [
      "hypogonadotropic hypogonadism 7 with or without anosmia",
      "hypogonadotropic hypogonadism 7 without anosmia",
      "HH7",
      "hypogonadism, isolated hypogonadotropic",
      "idiopathic hypogonadotropic hypogonadism"
    ],
    "categories": [
      {
        "ref": "MONDO:0005039",
        "name": "reproductive system disorder"
      },
      {
        "ref": "MONDO:0005151",
        "name": "endocrine system disorder"
      }
    ],
    "definition": "A hypogonadotropic hypogonadism that has material basis in homozygous or compound heterozygous mutation in the GNRHR gene on chromosome 4q13, sometimes in association with mutation in another gene. No patients with anosmia have been reported."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "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": [],
  "roots": [
    {
      "id": 16526,
      "label": "congenital hypogonadotropic hypogonadism"
    }
  ]
}