{
    "disease_id": "DOID:0070169", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013504", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013504", 
            "name": "spermatogenic failure type 8"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013504", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013504", 
            "name": "NR5A1 azoospermia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013504", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013504", 
            "name": "azoospermia caused by mutation in NR5A1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013504", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013504", 
            "name": "SPGF8"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013504", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013504", 
            "name": "spermatogenic failure 8; SPGF8"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070169", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070169", 
            "name": "SPGF8"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0070169", 
        "description": "A male infertility characterized by autosomal dominant inheritance of azoospermia or moderate to severe oligozoospermia that has_material_basis_in heterozygous mutation in the NR5A1 gene on chromosome 9q33.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0070169", 
        "name": "spermatogenic failure 8"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0070169#disease-associations", 
            "id": "0070169", 
            "database": "Alliance of Genome Resources"
        }
    ]
}