{
    "disease_id": "DOID:0070174", 
    "synonyms": [
        {
            "url": "http://disease-ontology.org/term/DOID:0070174", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070174", 
            "name": "SPGF17"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070174", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070174", 
            "name": "Male infertility due to oocyte activation failure"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014970", 
            "description": "Any azoospermia in which the cause of the disease is a mutation in the PLCZ1 gene.", 
            "resource": "MONDO", 
            "id": "MONDO:0014970", 
            "name": "spermatogenic failure 17"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014970", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014970", 
            "name": "spermatogenic failure type 17"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014970", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014970", 
            "name": "SPGF17"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014970", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014970", 
            "name": "Male infertility due to oocyte Activation failure"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014970", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014970", 
            "name": "PLCZ1 azoospermia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014970", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014970", 
            "name": "azoospermia caused by mutation in PLCZ1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014970", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014970", 
            "name": "spermatogenic failure 17"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014970", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014970", 
            "name": "spermatogenic failure 17; SPGF17"
        }, 
        {
            "url": "https://www.omim.org/entry/617214", 
            "description": "Spermatogenic failure 17", 
            "resource": "MIM", 
            "id": "MIM:617214", 
            "name": "Spermatogenic failure 17"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0070174", 
        "description": "A male infertility characterized by autosomal recessive inheritance of oocyte activation failure following intracytoplasmic sperm injection that has_material_basis_in mutation in the PLCZ1 gene on chromosome 12p12.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0070174", 
        "name": "spermatogenic failure 17"
    }
}