{
  "id": 14926,
  "label": "hypogonadotropic hypogonadism 12 with or without anosmia",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0013914",
  "properties": {
    "xrefs": [
      "DOID:0090072",
      "GARD:0000276",
      "MEDGEN:347328",
      "MESH:C535764",
      "OMIM:227200",
      "OMIM:614841",
      "UMLS:C1856897"
    ],
    "synonyms": [
      "eunuchoidism, familial hypogonadotropic",
      "hypogonadotropic hypogonadism 12 with or without anosmia",
      "FIGD",
      "HH12",
      "eunuchoidism familial hypogonadotropic",
      "familial hypogonadotropic eunuchoidism",
      "gonadotropin deficiency familial idiopathic",
      "gonadotropin deficiency, familial idiopathic"
    ],
    "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 mutation in the GNRH1 gene on chromosome 8p21."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 18569,
      "label": "hypogonadotropic hypogonadism",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4278,
        5714
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0090070",
          "DOID:7455",
          "GARD:0016533",
          "HP:0000044",
          "ICD9:253.4",
          "MEDGEN:82883",
          "NANDO:1200388",
          "NANDO:2100138",
          "NANDO:2200382",
          "NCIT:C113347",
          "OMIMPS:147950",
          "Orphanet:432",
          "SCTID:33927004",
          "UMLS:C0271623"
        ],
        "synonyms": [
          "Normosmic idiopathic hypogonadotropic hypogonadism",
          "central hypogonadism",
          "gonadotropic deficiency",
          "hypogonadism, hypogonadotropic",
          "hypogonadotropic hypogonadism",
          "hypogonadotropic hypogonadism with or without anosmia",
          "low gonadotropins (secondary hypogonadism)",
          "nIHH",
          "normosmic congenital hypogonadotropic hypogonadism",
          "secondary hypogonadism",
          "congenital idiopathic hypogonadotropic hypogonadism",
          "isolated congenital gonadotropin deficiency",
          "hypogonadotropism",
          "isolated hypogonadotropic hypogonadism"
        ],
        "categories": [
          {
            "ref": "MONDO:0005039",
            "name": "reproductive system disorder"
          },
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ],
        "definition": "Abnormal ovarian or testicular function due to insufficient hormonal stimulation from the hypothalamic-pituitary axis."
      },
      "child_count": 20,
      "reference_id": "MONDO:0018555"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 18569,
      "label": "hypogonadotropic hypogonadism"
    }
  ]
}