{
    "disease_id": "DOID:0070185",
    "recommended_name": {
        "id": "DOID:0070185",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0070185",
        "name": "X-linked spermatogenic failure 2",
        "description": "A spermatogenic failure that is 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."
    },
    "synonyms": [
        {
            "id": "DOID:0070185",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0070185",
            "name": "SPGFX2",
            "description": ""
        },
        {
            "id": "MONDO:0010647",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010647",
            "name": "spermatogenic failure, X-linked, 2",
            "description": "Any azoospermia in which the cause of the disease is a mutation in the TEX11 gene."
        },
        {
            "id": "MONDO:0010647",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010647",
            "name": "TEX11 azoospermia",
            "description": ""
        },
        {
            "id": "MONDO:0010647",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010647",
            "name": "azoospermia caused by mutation in TEX11",
            "description": ""
        },
        {
            "id": "MONDO:0010647",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010647",
            "name": "spermatogenic failure, X-linked, 2",
            "description": ""
        },
        {
            "id": "MONDO:0010647",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010647",
            "name": "spermatogenic failure, X-linked, 2, X-linked recessive",
            "description": ""
        },
        {
            "id": "MONDO:0010647",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010647",
            "name": "spermatogenic failure, X-linked, type 2",
            "description": ""
        },
        {
            "id": "MONDO:0010647",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010647",
            "name": "Male infertility from defect in meiosis",
            "description": ""
        },
        {
            "id": "MONDO:0010647",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010647",
            "name": "SPGFX2",
            "description": ""
        },
        {
            "id": "MIM:309120",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/309120",
            "name": "Spermatogenic failure, X-linked, 2",
            "description": "Spermatogenic failure, X-linked, 2"
        }
    ]
}