Conditions / Genetic
spermatogenic failure 48
info ยท Genetic
A spermatogenic failure that is characterized by impaired spermatogenesis, primarily occurring at meiosis that has_material_basis_in homozygous or compound heterozygous mutation in M1AP on chromosome 2p13.1.
Signs and symptoms
- Male infertility
- Oligozoospermia
- Azoospermia
- Spermatogenesis maturation arrest
Also known as: SPGF48