Term Name: spermatogenic failure 78
Synonyms: SPGF78
Definition: A spermatogenic failure characterized by sperm with abnormal acrosome structure due to a manchette assembly defect that has_material_basis_in homozygous mutation in the IQCN gene on chromosome 19p13.11.
Ontology: Human Disease [DOID:0070577]   ( DOID:0070577 )

Relationships
is a type of: autosomal recessive disease spermatogenic failure