Term Name: spermatogenic failure 37
Synonyms: SPGF37
Definition: A spermatogenic failure characterized by multiple morphologic abnormalities of the flagella, asthenoteratozoospermia, and infertility that has_material_basis_in homozygous or compound heterozygous mutation in the TTC21A gene on chromosome 3p22.2.
Ontology: Human Disease [DOID:0111927]   ( DOID:0111927 )

Relationships
is a type of: autosomal recessive disease spermatogenic failure