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Metadata
ID	DOID:0112273
Name	spermatogenic failure 51
Definition	A spermatogenic failure characterized by severe asthenoteratozoospermia with multiple morphologic abnormalities of the flagella resulting in reduced to absent motility that has_material_basis_in homozygous or compound heterozygous mutation in the CFAP91 gene on chromosome 3q13.33. https://pubmed.ncbi.nlm.nih.gov/32161152/
Xrefs	MIM:619177
Synonyms	SPGF51 [EXACT]
Parent Relationships	is_a spermatogenic failure is_a autosomal recessive disease
Subclass Logical Relationships	has material basis in some autosomal recessive inheritance