X-linked spermatogenic failure 8 Disease Ontology Browser

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Disease Ontology Browser

X-linked spermatogenic failure 8 (DOID:0070599)
Alliance: disease page
Synonyms: SPGFX8
Alt IDs: OMIM:301119
Definition: A spermatogenic failure characterized by sperm with head and midpiece defects, deformed and detached acrosomes, and markedly reduced progressive motility that has_material_basis_in hemizygous mutation in the CYLC1 gene on chromosome Xq21.1.

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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