{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010647", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010647", 
            "name": "spermatogenic failure, X-linked, 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010647", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010647", 
            "name": "spermatogenic failure, X-linked, 2; SPGFX2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010647", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010647", 
            "name": "Male infertility from defect in meiosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010647", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010647", 
            "name": "spermatogenic failure, X-linked, type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010647", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010647", 
            "name": "TEX11 azoospermia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010647", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010647", 
            "name": "SPGFX2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010647", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010647", 
            "name": "azoospermia caused by mutation in TEX11"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070185", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070185", 
            "name": "SPGFX2"
        }, 
        {
            "url": "https://www.omim.org/entry/309120", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:309120", 
            "name": "Spermatogenic failure, X-linked, 2"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0070185", 
        "description": "An azoospermia characterized by meiotic arrest of spermatocytes and mixed testicular atrophy that has_material_basis_in X-linked inheritance of mutation in the TEX11 gene on chromosome Xq13.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0070185", 
        "name": "X-linked spermatogenic failure 2"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/309120", 
            "id": "309120", 
            "database": "MIM"
        }
    ]
}