Term Name: spermatogenic failure 42
Synonyms: SPGF42
Definition: A spermatogenic failure characterized by multiple morphologic abnormalities of the flagella resulting in severly impaired sperm progressive motility and infertility that has_material_basis_in homozygous or compound heterozygous mutation in the TTC29 gene on chromosome 4q31.22.
Ontology: Human Disease [DOID:0111923]   ( DOID:0111923 )

Relationships
is a type of: autosomal recessive disease spermatogenic failure