{
  "id": 18747,
  "label": "Kallmann syndrome",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0018800",
  "properties": {
    "xrefs": [
      "DOID:3614",
      "GARD:0010771",
      "ICD9:253.4",
      "MEDGEN:102469",
      "MESH:D017436",
      "MedDRA:10053142",
      "NANDO:2200381",
      "NCIT:C75479",
      "NORD:1319",
      "Orphanet:478",
      "SCTID:93559003",
      "UMLS:C0162809"
    ],
    "synonyms": [
      "Olfacto-genital pathological sequence",
      "congenital hypogonadotropic hypogonadism with anosmia",
      "hypogonadotropic hypogonadism with anosmia"
    ],
    "categories": [
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      },
      {
        "ref": "MONDO:0005039",
        "name": "reproductive system disorder"
      },
      {
        "ref": "MONDO:0005151",
        "name": "endocrine system disorder"
      }
    ],
    "definition": "Kallmann syndrome (KS) is a developmental genetic disorder characterized by the association of congenital hypogonadotropic hypogonadism (CHH) due to gonadotropin-releasing hormone (GnRH) deficiency, and anosmia or hyposmia (with hypoplasia or aplasia of the olfactory bulbs)."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 18,
  "parents": [
    {
      "id": 4370,
      "label": "syndromic disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        29379
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:225",
          "MEDGEN:11688",
          "MESH:D013577",
          "NCIT:C28193",
          "OGMS:0000086",
          "UMLS:C0039082"
        ],
        "synonyms": [
          "cluster, symptom",
          "clusters, symptom",
          "symptom cluster",
          "symptom clusters",
          "syndrome",
          "syndrome associated with disease or disorder",
          "syndromes",
          "syndromic disease",
          "syndromic disease or disorder"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          }
        ],
        "definition": "A group of signs, symptoms, and clinicopathological characteristics that may or may not have a genetic basis and collectively define an abnormal condition."
      },
      "child_count": 1182,
      "reference_id": "MONDO:0002254"
    },
    {
      "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": [
    {
      "id": 9180,
      "label": "hypogonadotropic hypogonadism 2 with or without anosmia",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        18747
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0090083",
          "GARD:0003070",
          "MEDGEN:289648",
          "OMIM:147950",
          "UMLS:C1563720"
        ],
        "synonyms": [
          "FGFR1 hypogonadotropic hypogonadism",
          "hypogonadotropic hypogonadism 2 with or without anosmia",
          "hypogonadotropic hypogonadism caused by mutation in FGFR1",
          "HH2",
          "KAL2",
          "Kallmann syndrome 2"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0005039",
            "name": "reproductive system disorder"
          },
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ],
        "definition": "Any hypogonadotropic hypogonadism in which the cause of the disease is a mutation in the FGFR1 gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0007844"
    },
    {
      "id": 10708,
      "label": "hypogonadotropic hypogonadism 3 with or without anosmia",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        18747
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0090092",
          "GARD:0003073",
          "MEDGEN:763392",
          "OMIM:244200",
          "UMLS:C3550478"
        ],
        "synonyms": [
          "PROKR2 hypogonadotropic hypogonadism",
          "hypogonadotropic hypogonadism 3 with or without anosmia",
          "hypogonadotropic hypogonadism caused by mutation in PROKR2",
          "HH3",
          "KAL3",
          "Kallmann syndrome 3"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0005039",
            "name": "reproductive system disorder"
          },
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ],
        "definition": "Any hypogonadotropic hypogonadism in which the cause of the disease is a mutation in the PROKR2 gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0009482"
    },
    {
      "id": 11781,
      "label": "hypogonadotropic hypogonadism 1 with or without anosmia",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        18747
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0090094",
          "GARD:0003071",
          "MEDGEN:295872",
          "NCIT:C75480",
          "OMIM:308700",
          "UMLS:C1563719"
        ],
        "synonyms": [
          "ANOS1 hypogonadotropic hypogonadism",
          "hypogonadotropic hypogonadism 1 with or without anosmia",
          "hypogonadotropic hypogonadism 1 with or without anosmia (Kallmann syndrome 1), X-linked recessive",
          "hypogonadotropic hypogonadism caused by mutation in ANOS1",
          "HH1",
          "KAL1",
          "KMS",
          "Kallmann syndrome 1",
          "Kallmann syndrome, X-linked",
          "Kallmann syndrome, type 1, X-linked",
          "anosmic hypogonadism",
          "dysplasia Olfactogenitalis of De Morsier",
          "hypogonadotropic hypogonadism and anosmia"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0005039",
            "name": "reproductive system disorder"
          },
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ],
        "definition": "The X-linked inherited form of Kallmann syndrome caused by mutation of the KAL1 gene mapped to chromosome Xp22.3."
      },
      "child_count": 0,
      "reference_id": "MONDO:0010635"
    },
    {
      "id": 13576,
      "label": "hypogonadotropic hypogonadism 4 with or without anosmia",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        18747
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0090077",
          "GARD:0010772",
          "MEDGEN:765257",
          "MESH:C565696",
          "OMIM:610628",
          "UMLS:C3552343"
        ],
        "synonyms": [
          "PROK2 hypogonadotropic hypogonadism",
          "hypogonadotropic hypogonadism 4 with or without anosmia",
          "hypogonadotropic hypogonadism caused by mutation in PROK2",
          "KAL4",
          "Kallman syndrome 4",
          "HH4",
          "Kallmann syndrome 4"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0005039",
            "name": "reproductive system disorder"
          },
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ],
        "definition": "Any hypogonadotropic hypogonadism in which the cause of the disease is a mutation in the PROK2 gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0012528"
    },
    {
      "id": 13920,
      "label": "hypogonadotropic hypogonadism 5 with or without anosmia",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        18747
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0090084",
          "GARD:0010773",
          "MEDGEN:765467",
          "MESH:C567220",
          "OMIM:612370",
          "UMLS:C3552553"
        ],
        "synonyms": [
          "CHD7 hypogonadotropic hypogonadism",
          "hypogonadotropic hypogonadism 5 with or without anosmia",
          "hypogonadotropic hypogonadism caused by mutation in CHD7",
          "KAL5",
          "HH5",
          "Kallmann syndrome 5"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0005039",
            "name": "reproductive system disorder"
          },
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ],
        "definition": "Any hypogonadotropic hypogonadism in which the cause of the disease is a mutation in the CHD7 gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0012880"
    },
    {
      "id": 14028,
      "label": "hypogonadotropic hypogonadism 6 with or without anosmia",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        18747
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0090086",
          "GARD:0010774",
          "MEDGEN:765488",
          "MESH:C567199",
          "OMIM:612702",
          "UMLS:C3552574"
        ],
        "synonyms": [
          "FGF8 hypogonadotropic hypogonadism",
          "hypogonadotropic hypogonadism 6 with or without anosmia",
          "hypogonadotropic hypogonadism caused by mutation in FGF8",
          "KAL6",
          "HH6",
          "Kallmann syndrome 6"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0005039",
            "name": "reproductive system disorder"
          },
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ],
        "definition": "Any hypogonadotropic hypogonadism in which the cause of the disease is a mutation in the FGF8 gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0012988"
    },
    {
      "id": 14922,
      "label": "hypogonadotropic hypogonadism 8 with or without anosmia",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        18747
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0090074",
          "GARD:0015849",
          "MEDGEN:766755",
          "OMIM:614837",
          "UMLS:C3553841"
        ],
        "synonyms": [
          "KISS1R hypogonadotropic hypogonadism",
          "hypogonadotropic hypogonadism 8 with or without anosmia",
          "hypogonadotropic hypogonadism caused by mutation in KISS1R",
          "HH8"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0005039",
            "name": "reproductive system disorder"
          },
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ],
        "definition": "Any hypogonadotropic hypogonadism in which the cause of the disease is a mutation in the KISS1R gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0013910"
    },
    {
      "id": 14923,
      "label": "hypogonadotropic hypogonadism 9 with or without anosmia",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        18747
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0090085",
          "GARD:0015850",
          "MEDGEN:766756",
          "OMIM:614838",
          "UMLS:C3553842"
        ],
        "synonyms": [
          "NSMF hypogonadotropic hypogonadism",
          "hypogonadotropic hypogonadism 9 with or without anosmia",
          "hypogonadotropic hypogonadism caused by mutation in NSMF",
          "HH9"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0005039",
            "name": "reproductive system disorder"
          },
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ],
        "definition": "Any hypogonadotropic hypogonadism in which the cause of the disease is a mutation in the NSMF gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0013911"
    },
    {
      "id": 14925,
      "label": "hypogonadotropic hypogonadism 11 with or without anosmia",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        18747
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0090071",
          "GARD:0015851",
          "MEDGEN:766758",
          "OMIM:614840",
          "UMLS:C3553844"
        ],
        "synonyms": [
          "TACR3 hypogonadotropic hypogonadism",
          "hypogonadotropic hypogonadism 11 with or without anosmia",
          "hypogonadotropic hypogonadism caused by mutation in TACR3",
          "HH11"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0005039",
            "name": "reproductive system disorder"
          },
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ],
        "definition": "Any hypogonadotropic hypogonadism in which the cause of the disease is a mutation in the TACR3 gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0013913"
    },
    {
      "id": 14938,
      "label": "hypogonadotropic hypogonadism 14 with or without anosmia",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        18747
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0090087",
          "GARD:0015857",
          "MEDGEN:761703",
          "OMIM:614858",
          "UMLS:C3540450"
        ],
        "synonyms": [
          "WDR11 hypogonadotropic hypogonadism",
          "hypogonadotropic hypogonadism 14 with or without anosmia",
          "hypogonadotropic hypogonadism caused by mutation in WDR11",
          "HH14"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0005039",
            "name": "reproductive system disorder"
          },
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ],
        "definition": "Any hypogonadotropic hypogonadism in which the cause of the disease is a mutation in the WDR11 gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0013926"
    },
    {
      "id": 14957,
      "label": "hypogonadotropic hypogonadism 15 with or without anosmia",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        18747
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0090075",
          "GARD:0015872",
          "MEDGEN:766891",
          "OMIM:614880",
          "UMLS:C3553977"
        ],
        "synonyms": [
          "HS6ST1 hypogonadotropic hypogonadism",
          "hypogonadotropic hypogonadism 15 with or without anosmia",
          "hypogonadotropic hypogonadism caused by mutation in HS6ST1",
          "HH15"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0005039",
            "name": "reproductive system disorder"
          },
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ],
        "definition": "Any hypogonadotropic hypogonadism in which the cause of the disease is a mutation in the HS6ST1 gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0013946"
    },
    {
      "id": 14971,
      "label": "hypogonadotropic hypogonadism 16 with or without anosmia",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        18747
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0090080",
          "GARD:0015878",
          "MEDGEN:766935",
          "OMIM:614897",
          "UMLS:C3554021"
        ],
        "synonyms": [
          "SEMA3A hypogonadotropic hypogonadism",
          "hypogonadotropic hypogonadism 16 with or without anosmia",
          "hypogonadotropic hypogonadism caused by mutation in SEMA3A",
          "HH16"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0005039",
            "name": "reproductive system disorder"
          },
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ],
        "definition": "Any hypogonadotropic hypogonadism in which the cause of the disease is a mutation in the SEMA3A gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0013961"
    },
    {
      "id": 15111,
      "label": "hypogonadotropic hypogonadism 17 with or without anosmia",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        18747
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0090079",
          "GARD:0015928",
          "MEDGEN:815301",
          "OMIM:615266",
          "UMLS:C3808971"
        ],
        "synonyms": [
          "SPRY4 hypogonadotropic hypogonadism",
          "hypogonadotropic hypogonadism 17 with or without anosmia",
          "hypogonadotropic hypogonadism caused by mutation in SPRY4",
          "HH17"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0005039",
            "name": "reproductive system disorder"
          },
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ],
        "definition": "Any hypogonadotropic hypogonadism in which the cause of the disease is a mutation in the SPRY4 gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0014102"
    },
    {
      "id": 15112,
      "label": "hypogonadotropic hypogonadism 18 with or without anosmia",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        18747
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0090076",
          "GARD:0015929",
          "MEDGEN:815305",
          "OMIM:615267",
          "UMLS:C3808975"
        ],
        "synonyms": [
          "IL17RD hypogonadotropic hypogonadism",
          "hypogonadotropic hypogonadism 18 with or without anosmia",
          "hypogonadotropic hypogonadism 18 with or without anosmia, Autosomal recessive, Autosomal dominant, Digenic dominant",
          "hypogonadotropic hypogonadism caused by mutation in IL17RD",
          "HH18"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0005039",
            "name": "reproductive system disorder"
          },
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ],
        "definition": "Any hypogonadotropic hypogonadism in which the cause of the disease is a mutation in the IL17RD gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0014103"
    },
    {
      "id": 15114,
      "label": "hypogonadotropic hypogonadism 19 with or without anosmia",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        18747
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0090090",
          "GARD:0015931",
          "MEDGEN:815311",
          "OMIM:615269",
          "UMLS:C3808981"
        ],
        "synonyms": [
          "DUSP6 hypogonadotropic hypogonadism",
          "hypogonadotropic hypogonadism 19 with or without anosmia",
          "hypogonadotropic hypogonadism caused by mutation in DUSP6",
          "HH19"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0005039",
            "name": "reproductive system disorder"
          },
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ],
        "definition": "Any hypogonadotropic hypogonadism in which the cause of the disease is a mutation in the DUSP6 gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0014105"
    },
    {
      "id": 15115,
      "label": "hypogonadotropic hypogonadism 20 with or without anosmia",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        18747
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0090082",
          "GARD:0015932",
          "MEDGEN:815313",
          "OMIM:615270",
          "UMLS:C3808983"
        ],
        "synonyms": [
          "FGF17 hypogonadotropic hypogonadism",
          "hypogonadotropic hypogonadism 20 with or without anosmia",
          "hypogonadotropic hypogonadism caused by mutation in FGF17",
          "HH20"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0005039",
            "name": "reproductive system disorder"
          },
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ],
        "definition": "Any hypogonadotropic hypogonadism in which the cause of the disease is a mutation in the FGF17 gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0014106"
    },
    {
      "id": 15116,
      "label": "hypogonadotropic hypogonadism 21 with or without anosmia",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        18747
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0090093",
          "GARD:0015933",
          "MEDGEN:815316",
          "OMIM:615271",
          "UMLS:C3808986"
        ],
        "synonyms": [
          "FLRT3 hypogonadotropic hypogonadism",
          "hypogonadotropic hypogonadism 21 with anosmia",
          "hypogonadotropic hypogonadism 21 with or without anosmia",
          "hypogonadotropic hypogonadism caused by mutation in FLRT3",
          "HH21"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0005039",
            "name": "reproductive system disorder"
          },
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ],
        "definition": "Any hypogonadotropic hypogonadism in which the cause of the disease is a mutation in the FLRT3 gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0014107"
    },
    {
      "id": 15461,
      "label": "hypogonadotropic hypogonadism 22 with or without anosmia",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        18747
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0090081",
          "GARD:0016050",
          "MEDGEN:863425",
          "OMIM:616030",
          "UMLS:C4014988"
        ],
        "synonyms": [
          "FEZF1 hypogonadotropic hypogonadism",
          "hypogonadotropic hypogonadism 22 with or without anosmia",
          "hypogonadotropic hypogonadism 22, with or without anosmia",
          "hypogonadotropic hypogonadism caused by mutation in FEZF1",
          "HH22"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0005039",
            "name": "reproductive system disorder"
          },
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ],
        "definition": "Any hypogonadotropic hypogonadism in which the cause of the disease is a mutation in the FEZF1 gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0014461"
    }
  ],
  "roots": [
    {
      "id": 4370,
      "label": "syndromic disease"
    },
    {
      "id": 18569,
      "label": "hypogonadotropic hypogonadism"
    }
  ]
}