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hereditary Wilms tumor

Disease Summary
Associated Targets (15)
Tbio

11

Tchem

3

Tclin

1


Mondo Description Familial embryonal neoplasm derived from nephrogenic blastemal cells. Several lines of differentiation, including blastemal, stromal and epithelial, are usually expressed. Comprises approximately 1% of Wilms tumors. (AFIP fascicle version 2.0)
Disease Ontology Description A nephroblastoma that results_in either bilateral disease or a family history of Wilms' tumour.
Mondo Term and Equivalent IDs
MONDO:0003321:  hereditary Wilms tumor
NCIT:C8496: 
OMIMPS:194070: 
UMLS:C0677779: