{
    "disease_id": "DOID:0090094",
    "recommended_name": {
        "id": "DOID:0090094",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0090094",
        "name": "hypogonadotropic hypogonadism 1 with or without anosmia",
        "description": "A hypogonadotropic hypogonadism that has_material_basis_in mutation in the KAL1 gene on chromosome Xp22.3, sometimes in association with mutation in another gene."
    },
    "synonyms": [
        {
            "id": "DOID:0090094",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0090094",
            "name": "dysplasia olfactogenitalis of de morsier",
            "description": ""
        },
        {
            "id": "MONDO:0010635",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010635",
            "name": "hypogonadotropic hypogonadism 1 with or without anosmia",
            "description": "The X-linked inherited form of Kallmann syndrome caused by mutation of the KAL1 gene mapped to chromosome Xp22.3."
        },
        {
            "id": "MONDO:0010635",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010635",
            "name": "ANOS1 hypogonadotropic hypogonadism",
            "description": ""
        },
        {
            "id": "MONDO:0010635",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010635",
            "name": "dysplasia olfactogenitalis of de Morsier",
            "description": ""
        },
        {
            "id": "MONDO:0010635",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010635",
            "name": "hypogonadotropic hypogonadism 1 with or without anosmia",
            "description": ""
        },
        {
            "id": "MONDO:0010635",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010635",
            "name": "hypogonadotropic hypogonadism 1 with or without anosmia (Kallmann syndrome 1), X-linked recessive",
            "description": ""
        },
        {
            "id": "MONDO:0010635",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010635",
            "name": "hypogonadotropic hypogonadism caused by mutation in ANOS1",
            "description": ""
        },
        {
            "id": "MONDO:0010635",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010635",
            "name": "HH1",
            "description": ""
        },
        {
            "id": "MONDO:0010635",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010635",
            "name": "KAL1",
            "description": ""
        },
        {
            "id": "MONDO:0010635",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010635",
            "name": "KMS",
            "description": ""
        },
        {
            "id": "MONDO:0010635",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010635",
            "name": "Kallmann syndrome 1",
            "description": ""
        },
        {
            "id": "MONDO:0010635",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010635",
            "name": "Kallmann syndrome, X-linked",
            "description": ""
        },
        {
            "id": "MONDO:0010635",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010635",
            "name": "Kallmann syndrome, type 1, X-linked",
            "description": ""
        },
        {
            "id": "MONDO:0010635",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010635",
            "name": "anosmic hypogonadism",
            "description": ""
        },
        {
            "id": "MONDO:0010635",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010635",
            "name": "dysplasia Olfactogenitalis of De Morsier",
            "description": ""
        },
        {
            "id": "MONDO:0010635",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010635",
            "name": "hypogonadotropic hypogonadism and anosmia",
            "description": ""
        },
        {
            "id": "MIM:308700",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/308700",
            "name": "Hypogonadotropic hypogonadism 1 with or without anosmia",
            "description": "Hypogonadotropic hypogonadism 1 with or without anosmia"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0090094"
    ],
    "unlinked_id_list": []
}