Term Name: X-linked spermatogenic failure 2
Synonyms: SPGFX2
Definition: A spermatogenic failure that is characterized by meiotic arrest of spermatocytes and mixed testicular atrophy that has_material_basis_in X-linked inheritance of mutation in the TEX11 gene on chromosome Xq13.
Ontology: Human Disease [DOID:0070185]   ( DOID:0070185 )

Relationships
is a type of: spermatogenic failure X-linked recessive disease