Term Name: spermatogenic failure 19
Synonyms: SPGF19
Definition: A spermatogenic failure that is characterized by autosomal recessive inheritance of sperm flagellar morphological abnormalities that has_material_basis_in mutation in the CFAP43 gene on chromosome 10q25.
Ontology: Human Disease [DOID:0070170]   ( DOID:0070170 )

Relationships
is a type of: autosomal recessive disease spermatogenic failure