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Metadata
ID	DOID:0111912
Name	spermatogenic failure 41
Definition	A spermatogenic failure characterized by oligozoospermia and multiple morphologic abnormalities of the flagella that has_material_basis_in homozygous or compound heterozygous mutation in the CFAP70 gene on chromosome 10q22.2. https://pubmed.ncbi.nlm.nih.gov/31621862/
Xrefs	MIM:618670
Synonyms	SPGF41 [EXACT]
Parent Relationships	is_a spermatogenic failure is_a autosomal recessive disease
Subclass Logical Relationships	has material basis in some autosomal recessive inheritance