{
    "disease_id": "DOID:0111928", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0054731", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0054731", 
            "name": "SPGF27"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0054731", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0054731", 
            "name": "spermatogenic failure 27; SPGF27"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111928", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111928", 
            "name": "SPGF27"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111928", 
        "description": "A spermatogenic failure characterized by multiple morphologic abnormalities of the sperm flagella, loss of the central pair of microtubules, loss of the inner dynein arms, and peripheral doublet disorganization of the flagella that has_material_basis_in homozygous or compound heterozygous mutation in AK7 on chromosome 14q32.2.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111928", 
        "name": "spermatogenic failure 27"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111928#disease-associations", 
            "id": "0111928", 
            "database": "Alliance of Genome Resources"
        }
    ]
}