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| Term | X-linked spermatogenic failure 2 | ID (Ontology) | DOID:0070185 (Human Disease) |
| Definition | 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. | ||
| Also Known As | "SPGFX2" | ||
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X-linked monogenic disease |__X-linked recessive disease__ male infertility | |__spermatogenic failure_______| X-linked spermatogenic failure 2 |
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X-linked recessive disease spermatogenic failure |
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| MIM:309120 | |||