Term Name: spermatogenic failure 49
Synonyms: SPGF98
Definition: A spermatogenic failure characterized by multiple morphologic abnormalities of the sperm flagella resulting in markedly reduced or no progressive motility that has_material_basis_in homozygous or compound heterozygous mutation in the CFAP58 gene on chromosome 10q25.1.
Ontology: Human Disease [DOID:0112271]   ( DOID:0112271 )

Relationships
is a type of: autosomal recessive disease spermatogenic failure