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Summary Literature (0)
DOID:0050438 - Frasier syndrome

Disease Ontology Definition:A syndrome that is characterized by gonadal dysgenesis, streak gonads, progressive focal segmental glomerulonephropathy and the development of urogenital cancers that is the result of mutation in the WT1 gene.

Synonyms:

Xenbase Genes : wt1

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0007635 - nucleus of medulla oblongata

MIM:
MIM:136680 - FRASIER SYNDROME

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), syndrome (is_a)