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Metadata
ID	DOID:0111927
Name	spermatogenic failure 37
Definition	A spermatogenic failure characterized by multiple morphologic abnormalities of the flagella, asthenoteratozoospermia, and infertility that has_material_basis_in homozygous or compound heterozygous mutation in the TTC21A gene on chromosome 3p22.2. https://pubmed.ncbi.nlm.nih.gov/30929735/
Xrefs	MIM:618429
Synonyms	SPGF37 [EXACT]
Parent Relationships	is_a spermatogenic failure is_a autosomal recessive disease
Subclass Logical Relationships	has material basis in some autosomal recessive inheritance