You are using an outdated browser. Please upgrade your browser to improve your experience.

spermatogenic failure 18

Disease Summary
Associated Targets (1)
Tbio

1


Uniprot Description An infertility disorder caused by spermatogenesis defects and characterized by abnormally shaped spermatozoa in the semen of affected individuals. SPGF18 patients present with primary infertility and multiple morphological abnormalities of sperm flagella that result in impaired sperm mobility. Abnormalities include absent, short, coiled, bent, and irregular flagella. SPGF18 inheritance is autosomal recessive.
Mondo Term and Equivalent IDs
MONDO:0054615:  spermatogenic failure 18