Term Name: spermatogenic failure 38
Synonyms: SPGF38
Definition: A spermatogenic failure characterized by multiple morphologic abnormalities of the flagella resulting in infertility and asthenoteratozoospermia that has_material_basis_in homozygous or compound heterozygous mutation in the ARMC2 gene on chromosome 6q21.
Ontology: Human Disease [DOID:0111919]   ( DOID:0111919 )

Relationships
is a type of: autosomal recessive disease spermatogenic failure