{
    "disease_id": "DOID:0090082", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014106", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014106", 
            "name": "hypogonadotropic hypogonadism 20 with or without anosmia; HH20"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014106", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014106", 
            "name": "FGF17 hypogonadotropic hypogonadism"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014106", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014106", 
            "name": "hypogonadotropic hypogonadism caused by mutation in FGF17"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014106", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014106", 
            "name": "HH20"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0090082", 
        "description": "A hypogonadotropic hypogonadism that has_material_basis_in heterozygous mutation in the FGF17 gene on chromosome 8p21, sometimes in association with mutations in other genes.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0090082", 
        "name": "hypogonadotropic hypogonadism 20 with or without anosmia"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0090082#disease-associations", 
            "id": "0090082", 
            "database": "Alliance of Genome Resources"
        }
    ]
}