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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:

In OMIM:
OMIM:136680 - FRASIER SYNDROME

In Mondo Disease Ontology:
MONDO:0007635 - Frasier syndrome

Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Xenbase Genes : wt1

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Parent(s): autosomal dominant disease (is_a), syndrome (is_a)