Conditions / Genetic
spermatogenic failure 10
info ยท Genetic
A spermatogenic failure that is characterized by defects in the annulus or the ring-like structure located at the distal end of the flagellar midpiece the autosomal dominant inheritance of that has_material_basis_in mutation in the SEPT12 gene on chromosome 16
A spermatogenic failure that is characterized by defects in the annulus or the ring-like structure located at the distal end of the flagellar midpiece the autosomal dominant inheritance of that has_material_basis_in mutation in the SEPT12 gene on chromosome 16p13.
Signs and symptoms
- Male infertility
- Abnormal sperm morphology
- Reduced sperm motility
- Oligozoospermia
Also known as: SPGF10; Spermatogenic failure with defective sperm annulus