{
    "disease_id": "DOID:0090078", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007794", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007794", 
            "name": "idiopathic hypogonadotropic hypogonadism"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007794", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007794", 
            "name": "hypogonadism, isolated hypogonadotropic"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007794", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007794", 
            "name": "hypogonadotropic hypogonadism 7 with or without anosmia; HH7"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007794", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007794", 
            "name": "HH7"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0090078", 
        "description": "A hypogonadotropic hypogonadism that has_material_basis_in homozygous or compound heterozygous mutation in the GNRHR gene on chromosome 4q13, sometimes in association with mutation in another gene. No patients with anosmia have been reported.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0090078", 
        "name": "hypogonadotropic hypogonadism 7 with or without anosmia"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0090078#disease-associations", 
            "id": "0090078", 
            "database": "Alliance of Genome Resources"
        }
    ]
}