{
    "disease_id": "DOID:0090080", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013961", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013961", 
            "name": "HH16"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013961", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013961", 
            "name": "hypogonadotropic hypogonadism 16 with or without anosmia; HH16"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013961", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013961", 
            "name": "hypogonadotropic hypogonadism caused by mutation in SEMA3A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013961", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013961", 
            "name": "SEMA3A hypogonadotropic hypogonadism"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0090080", 
        "description": "A hypogonadotropic hypogonadism that has_material_basis_in mutation in the SEMA3A gene on chromosome 7, sometimes in association with mutations in other genes.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0090080", 
        "name": "hypogonadotropic hypogonadism 16 with or without anosmia"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0090080#disease-associations", 
            "id": "0090080", 
            "database": "Alliance of Genome Resources"
        }
    ]
}