Term Name: spermatogenic failure 39
Synonyms: SPGF39
Definition: A spermatogenic failure characterized by multiple morphologic anomalies of the sperm flagellum, lack of the outer dynein arms in the flagella, and asthenozoospermia that has_material_basis_in homozygous or compound heterozygous mutation in the DNAH17 gene on chromosome 17q25.3.
Ontology: Human Disease [DOID:0111926]   ( DOID:0111926 )

Relationships
is a type of: autosomal recessive disease spermatogenic failure