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Summary Literature (0)
DOID:0111913 - spermatogenic failure 30

Disease Ontology Definition:A spermatogenic failure characterized by nonobstructive azoospermia or cryptozoospermia that has_material_basis_in homozygous or compound heterozygous mutation in the TDRD9 gene on chromosome 14q32.33.

Synonyms: SPGF30,

Xenbase Genes : tdrd9

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

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