{
    "disease_id": "DOID:0111921", 
    "synonyms": [
        {
            "url": "http://disease-ontology.org/term/DOID:0111921", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111921", 
            "name": "SPGF36"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111921", 
        "description": "A spermatogenic failure characterized by spermatozoa showing anomalies of the head, acrosome, and nucleus of the sperm resulting in reduced fertility that has_material_basis_in heterozygous mutation in PPP2R3C on chromosome 14q13.2.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111921", 
        "name": "spermatogenic failure 36"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/618420", 
            "id": "618420", 
            "database": "MIM"
        }
    ]
}