{
    "disease_id": "DOID:0111156", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013505", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013505", 
            "name": "spermatogenic failure type 9"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013505", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013505", 
            "name": "globozoospermia, total"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013505", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013505", 
            "name": "DPY19L2 azoospermia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013505", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013505", 
            "name": "SPGF9"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013505", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013505", 
            "name": "globozoospermia, complete"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013505", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013505", 
            "name": "azoospermia caused by mutation in DPY19L2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013505", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013505", 
            "name": "spermatogenic failure 9; SPGF9"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111156", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111156", 
            "name": "globozoospermia"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111156", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111156", 
            "name": "male infertility due to globozoospermia"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111156", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111156", 
            "name": "male infertility due to round-headed spermatozoa"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111156", 
        "description": "A male infertility characterized by round-headed spermatozoa lacking an acrosome and that has_material_basis_in autosomal recessive inheritance in a mutation in the DPY19L2 gene on chromosome 12q14.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111156", 
        "name": "spermatogenic failure 9"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111156#disease-associations", 
            "id": "0111156", 
            "database": "Alliance of Genome Resources"
        }
    ]
}