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Human Disease

X-linked spermatogenic failure 7

Term ID
DOID:0070598
Synonyms
  • SPGFX7
Definition
A spermatogenic failure characterized by sperm with insufficient individualization, excessive residual cytoplasm, acrosome defects, and abnormalities of the head and flagella, resulting in significantly reduced sperm concentration and progressive motility, that has_material_basis_in hemizygous mutation in the CT55 gene on chromosome Xq26.3. https://pubmed.ncbi.nlm.nih.gov/36481789/
References
Ontology
Human Disease   ( DOID:0070598 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models