Search Ontology:
Human Disease

X-linked spermatogenic failure 8

Term ID
DOID:0070599
Synonyms
  • SPGFX8
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. (2)
References
Ontology
Human Disease   ( DOID:0070599 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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