Term Name: spermatogenic failure 22
Synonyms: SPGF22
Definition: A spermatogenic failure that is characterized by autosomal recessive inheritance of spermatocyte maturation arrest resulting in azoospermia that has_material_basis_in mutation in the MEIOB gene on chromosome 16p13.
Ontology: Human Disease [DOID:0070177]   ( DOID:0070177 )

Relationships
is a type of: autosomal recessive disease spermatogenic failure