Term Name: spermatogenic failure 89
Synonyms: SPGF89
Definition: A spermatogenic failure characterized by severely reduced progressive motility of sperm that has_material_basis_in homozygous or compound heterozygous mutation in the AK9 gene on chromosome 6q21.
Ontology: Human Disease [DOID:0070588]   ( DOID:0070588 )

Relationships
is a type of: autosomal recessive disease spermatogenic failure