Mondo Description Any azoospermia in which the cause of the disease is a mutation in the SYCE1 gene.

Uniprot Description An infertility disorder caused by spermatogenesis defects and characterized by non-obstructive azoospermia due to complete meiotic maturation arrest. SPGF15 inheritance is autosomal recessive.

Disease Ontology Description An azoospermia characterized by autosomal recessive inheritance of azoospermia that has_material_basis_in mutation in the SYCE1 gene on chromosome 10q26.