Term Name: spermatogenic failure 51
Synonyms: SPGF51
Definition: A spermatogenic failure characterized by severe asthenoteratozoospermia with multiple morphologic abnormalities of the flagella resulting in reduced to absent motility that has_material_basis_in homozygous or compound heterozygous mutation in the CFAP91 gene on chromosome 3q13.33.
Ontology: Human Disease [DOID:0112273]   ( DOID:0112273 )

Relationships
is a type of: autosomal recessive disease spermatogenic failure