{
    "disease_id": "DOID:0070168", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011720", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011720", 
            "name": "SPGF3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011720", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011720", 
            "name": "spermatogenic failure type 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011720", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011720", 
            "name": "SLC26A8 azoospermia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011720", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011720", 
            "name": "azoospermia caused by mutation in SLC26A8"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011720", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011720", 
            "name": "spermatogenic failure 3; SPGF3"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070168", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070168", 
            "name": "SPGF3"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0070168", 
        "description": "A male infertility characterized by autosomal dominant inheritance of nonobstructive asthenozoospermia that has_material_basis_in heterozygous mutation in the SLC26A8 gene on chromosome 6p21.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0070168", 
        "name": "spermatogenic failure 3"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0070168#disease-associations", 
            "id": "0070168", 
            "database": "Alliance of Genome Resources"
        }
    ]
}