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Metadata
ID	DOID:0070180
Name	spermatogenic failure 11
Definition	A spermatogenic failure that is characterized by autosomal dominant inheritance of oligozoospermia and in some cases teratozoospermia and/or moderate asthenozoospermia that has_material_basis_in mutation in the KLHL10 gene on chromosome 17q21. https://www.ncbi.nlm.nih.gov/pubmed/17047026
Xrefs	MIM:615081
Synonyms	SPGF11 [EXACT]
Parent Relationships	is_a autosomal dominant disease is_a spermatogenic failure
Subclass Logical Relationships	has material basis in some autosomal dominant inheritance