{
    "disease_id": "DOID:0090086",
    "recommended_name": {
        "id": "DOID:0090086",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0090086",
        "name": "hypogonadotropic hypogonadism 6 with or without anosmia",
        "description": "A hypogonadotropic hypogonadism that is characterized by autosomal dominant inheritance and has_material_basis_in heterozygous mutation in the FGF8 gene on chromosome 10q24, sometimes in association with mutation in another gene."
    },
    "synonyms": [
        {
            "id": "MONDO:0012988",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012988",
            "name": "hypogonadotropic hypogonadism 6 with or without anosmia",
            "description": "Any hypogonadotropic hypogonadism in which the cause of the disease is a mutation in the FGF8 gene."
        },
        {
            "id": "MONDO:0012988",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012988",
            "name": "FGF8 hypogonadotropic hypogonadism",
            "description": ""
        },
        {
            "id": "MONDO:0012988",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012988",
            "name": "hypogonadotropic hypogonadism 6 with or without anosmia",
            "description": ""
        },
        {
            "id": "MONDO:0012988",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012988",
            "name": "hypogonadotropic hypogonadism caused by mutation in FGF8",
            "description": ""
        },
        {
            "id": "MONDO:0012988",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012988",
            "name": "KAL6",
            "description": ""
        },
        {
            "id": "MONDO:0012988",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012988",
            "name": "HH6",
            "description": ""
        },
        {
            "id": "MONDO:0012988",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012988",
            "name": "Kallmann syndrome 6",
            "description": ""
        },
        {
            "id": "MIM:612702",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/612702",
            "name": "Hypogonadotropic hypogonadism 6 with or without anosmia",
            "description": "Hypogonadotropic hypogonadism 6 with or without anosmia"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0090086"
    ],
    "unlinked_id_list": []
}