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Summary Literature (0)
DOID:0070171 - spermatogenic failure 12

Disease Ontology 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.

Synonyms: SPGF12,

Xenbase Genes : nanos1

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014172 - spermatogenic failure 12


Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal dominant disease (is_a), spermatogenic failure (is_a)