Term Name: spermatogenic failure 35
Synonyms: SPGF35
Definition: A spermatogenic failure characterized by multiple morphologic abnormalities of the flagella resulting in severely impaired sperm motility and infertility that has_material_basis_in homozygous or compound heterozygous mutation in the QRICH2 gene on chromosome 17q25.1.
Ontology: Human Disease [DOID:0111914]   ( DOID:0111914 )

Relationships
is a type of: autosomal recessive disease spermatogenic failure