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Metadata
ID	DOID:0111919
Name	spermatogenic failure 38
Definition	A spermatogenic failure characterized by multiple morphologic abnormalities of the flagella resulting in infertility and asthenoteratozoospermia that has_material_basis_in homozygous or compound heterozygous mutation in the ARMC2 gene on chromosome 6q21. https://pubmed.ncbi.nlm.nih.gov/30686508/
Xrefs	MIM:618433
Synonyms	SPGF38 [EXACT]
Parent Relationships	is_a spermatogenic failure is_a autosomal recessive disease
Subclass Logical Relationships	has material basis in some autosomal recessive inheritance