{
    "disease_id": "DOID:0090094", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010635", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010635", 
            "name": "hypogonadotropic hypogonadism 1 with or without anosmia; HH1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010635", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010635", 
            "name": "KAL1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010635", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010635", 
            "name": "hypogonadotropic hypogonadism and anosmia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010635", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010635", 
            "name": "anosmic hypogonadism"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010635", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010635", 
            "name": "Kallmann syndrome, X-linked"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010635", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010635", 
            "name": "dysplasia Olfactogenitalis of De Morsier"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010635", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010635", 
            "name": "Kallmann syndrome, type 1, X-linked"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010635", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010635", 
            "name": "KMS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010635", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010635", 
            "name": "ANOS1 hypogonadotropic hypogonadism"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010635", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010635", 
            "name": "HH1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010635", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010635", 
            "name": "hypogonadotropic hypogonadism caused by mutation in ANOS1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010635", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010635", 
            "name": "Kallmann syndrome 1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0090094", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0090094", 
            "name": "dysplasia olfactogenitalis of de morsier"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0090094", 
        "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.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0090094", 
        "name": "hypogonadotropic hypogonadism 1 with or without anosmia"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/308700", 
            "id": "308700", 
            "database": "MIM"
        }
    ]
}