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Metadata
ID	DOID:0112271
Name	spermatogenic failure 49
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. https://pubmed.ncbi.nlm.nih.gov/32791035/
Xrefs	MIM:619144
Synonyms	SPGF98 [EXACT]
Parent Relationships	is_a spermatogenic failure is_a autosomal recessive disease
Subclass Logical Relationships	has material basis in some autosomal recessive inheritance