Term Name: spermatogenic failure 41
Synonyms: SPGF41
Definition: A spermatogenic failure characterized by oligozoospermia and multiple morphologic abnormalities of the flagella that has_material_basis_in homozygous or compound heterozygous mutation in the CFAP70 gene on chromosome 10q22.2.
Ontology: Human Disease [DOID:0111912]   ( DOID:0111912 )

Relationships
is a type of: autosomal recessive disease spermatogenic failure