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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:
Echinobase Genes
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	| MIM:136680 - frasier syndrome | 
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view
Parent(s): 
			
				
					autosomal dominant disease (is_a), 
				
				
			
				
					syndrome (is_a)
				
				
			
		
		