Genetic Predisposition to Non-Syndromic Wilms Tumor

Preferred Label : Genetic Predisposition to Non-Syndromic Wilms Tumor;

NCIt definition : A genetic predisposition to Wilms tumor due to germline mutation(s) in the REST, TRIM28, or CTR9 genes, encoding RE1-silencing transcription factor, transcription intermediary factor 1-beta, and RNA polymerase-associated protein CTR9 homolog, respectively.;

NCI Metathesaurus CUI : CL1647848;

Details

Origin ID

C178392;

UMLS CUI

C5555002;

Semantic type(s)
- Finding [UMLS semantic type]
concept_is_in_subset
- CCPS Disease Terminology [NCIt concept]
- Childhood Cancer Predisposition Study Terminology [NCIt concept]
related_to_genetic_biomarker
- CTR9 Gene [NCIt concept]
- REST Gene [NCIt concept]
- TRIM28 Gene [NCIt concept]

Keyword's position in hierarchy(ies) :

You can consult :

All resources
or only the major
or use the search engine

recommendations
documents concerning education
documents for patients