{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014172", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014172", 
            "name": "azoospermia caused by mutation in NANOS1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014172", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014172", 
            "name": "spermatogenic failure type 12"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014172", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014172", 
            "name": "spermatogenic failure 12; SPGF12"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014172", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014172", 
            "name": "SPGF12"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014172", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014172", 
            "name": "NANOS1 azoospermia"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070171", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070171", 
            "name": "SPGF12"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0070171", 
        "description": "A male infertility characterized by autosomal dominant inheritance of azoospermia or severe oligoasthenoteratozoospermia and in some cases a Sertolic cell-only phenotype that has_material_basis_in heterozygous mutation in the NANOS1 gene on chromosome 10q26.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0070171", 
        "name": "spermatogenic failure 12"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/615413", 
            "id": "615413", 
            "database": "MIM"
        }
    ]
}