Wilms Tumor 2; Wt2

Table of contents:

Description
Related genes
Clinical Features
Incidence and onset information
Alternative Names
Researches and researchers
Gene Panels
Sources and references

Genes related to Wilms Tumor 2; Wt2

Clinical Features

Phenotypes and symptoms related to Wilms Tumor 2; Wt2

Neoplasm
Nephroblastoma

Incidence and onset information

— Currently we don't have prevalence information about this disease (Not enough data available about incidence and published cases.)
— No data available about the known clinical features onset.

Researches and researchers

Currently, we don't have any information about doctors, researches or researchers related to this disease. Please contact us if you would like to appear here.

Wilms Tumor 2; Wt2 Recommended genes panels

Panel Name, Specifity and genes Tested/covered
Chromosome 11-related Beckwith-Wiedemann Syndrome. By Clinical Molecular Genetics Laboratory Johns Hopkins All Children's Hospital (United States). H19, KCNQ1OT1 Specificity 50 % Genes 100 %
Test for Beckwith-Wiedemann Syndrome. By Genome Diagnostics Laboratory University Medical Center Utrecht (Netherlands). CDKN1C, H19, KCNQ1OT1 Specificity 34 % Genes 100 %
Test for Chromosome 11p15.5-Related Russell-Silver Syndrome. By Genome Diagnostics Laboratory University Medical Center Utrecht (Netherlands). H19 Specificity 100 % Genes 100 %
Beckwith-Wiedemann Syndrome. By Genetics Laboratory Shodair Children's Hospital (United States). H19, KCNQ1 Specificity 50 % Genes 100 %
Russell-Silver Syndrome. By Genetics Laboratory Shodair Children's Hospital (United States). H19 Specificity 100 % Genes 100 %
Beckwith-Wiedemann Syndrome (methylation test). By Laboratory of genome diagnostics Academic Medical Center, University of Amsterdam (Netherlands). H19, KCNQ1OT1 Specificity 50 % Genes 100 %
Silver-Russel Syndrome (11p15). By Laboratory of genome diagnostics Academic Medical Center, University of Amsterdam (Netherlands). H19 Specificity 100 % Genes 100 %
Isolated hemihyperplasia (methylation analysis of KCNQ1OT1 and H19 genes). By CGC Genetics (Portugal). H19, KCNQ1OT1 Specificity 50 % Genes 100 %

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Sources and references

You can check the following sources for additional information.

OMIM MESH Genetic Syndrome Finder

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