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Metadata
ID	DOID:0070171
Name	spermatogenic failure 12
Definition	A spermatogenic failure that is characterized by autosomal dominant inheritance of azoospermia or severe oligoasthenoteratozoospermia and in some cases a Sertolic cell-only phenotype that has_material_basis_in heterozygous mutation in the NANOS1 gene on chromosome 10q26. https://www.ncbi.nlm.nih.gov/pubmed/23315541
Xrefs	MIM:615413
Synonyms	SPGF12 [EXACT]
Parent Relationships	is_a autosomal dominant disease is_a spermatogenic failure
Subclass Logical Relationships	has material basis in some autosomal dominant inheritance