Term Name: spermatogenic failure 7
Synonyms: SPGF7
Definition: A spermatogenic failure that is characterized by autosomal recessive inheritance of impaired or absent sperm motility and increased incidence of morphologically abnormal sperm that has_material_basis_in mutation in the CATSPER1 gene on chromosome 11q13.
Ontology: Human Disease [DOID:0070173]   ( DOID:0070173 )

Relationships
is a type of: autosomal recessive disease spermatogenic failure