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Summary Literature (0)
DOID:0070169 - spermatogenic failure 8

Disease Ontology Definition:A spermatogenic failure that is characterized by autosomal dominant inheritance of azoospermia or moderate to severe oligozoospermia that has_material_basis_in heterozygous mutation in the NR5A1 gene on chromosome 9q33.

Synonyms: SPGF8

Xenbase Genes : nr5a1

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013504 - caudal vertebra pre-cartilage condensation

MIM:
MIM:613957 - SPERMATOGENIC FAILURE 8; SPGF8

Other Model Organisms: Alliance, 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)