{
    "disease_id": "DOID:0070184", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014961", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014961", 
            "name": "spermatogenic failure type 16"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014961", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014961", 
            "name": "azoospermia caused by mutation in SUN5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014961", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014961", 
            "name": "acephalic spermatozoa syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014961", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014961", 
            "name": "SUN5 azoospermia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014961", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014961", 
            "name": "SPGF16"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014961", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014961", 
            "name": "spermatogenic failure 16; SPGF16"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070184", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070184", 
            "name": "SPGF16"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070184", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070184", 
            "name": "acephalic spermatozoa syndrome"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0070184", 
        "description": "A male infertility characterized by autosomal recessive inheritance of acephalic spermatozoa that has_material_basis_in mutation in the SUN5 gene on chromosome 20q11.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0070184", 
        "name": "spermatogenic failure 16"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0070184#disease-associations", 
            "id": "0070184", 
            "database": "Alliance of Genome Resources"
        }
    ]
}