Wilms Tumor 6; Wt6

Clinical Features

Phenotypes and symptoms related to Wilms Tumor 6; Wt6

  • 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.

Alternative names

Wilms Tumor 6; Wt6 Is also known as wilms tumor, susceptibility to.

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 6; Wt6 Recommended genes panels

Panel Name, Specifity and genes Tested/covered
Cancer Sequencing Panel with CNV Detection.

By PreventionGenetics PreventionGenetics (United States).

RUNX1, BLM, SDHA, SDHB, SDHC, SDHD, BMPR1A, BRCA1, BRCA2, SMARCA4, SMARCB1, SMARCE1, SRP72, STK11, EPCAM, TERC, TERT, TP53, TRIP13, TSC1 , (...)

View the complete list with 78 more genes
Specificity
2 %
Genes
100 %
REST.

By Fulgent Genetics Fulgent Genetics (United States).

REST
Specificity
100 %
Genes
100 %
Hereditary Pediatric Cancer Panel.

By Blueprint Genetics (Finland).

RIT1, RRAS, RUNX1, BLM, SDHA, SDHB, SDHC, SDHD, BMPR1A, BRAF, SMARCA4, SMARCB1, SOS1, SOS2, STK11, BUB1B, EPCAM, TP53, TSC1, TSC2 , (...)

View the complete list with 51 more genes
Specificity
2 %
Genes
100 %
Comprehensive Hereditary Cancer Panel.

By Blueprint Genetics (Finland).

RIT1, RRAS, RUNX1, BLM, SDHA, SDHB, SDHC, SDHD, BMPR1A, BRAF, BRCA1, BRCA2, SMARCA4, SMARCB1, SOS1, SOS2, SRP72, STK11, BUB1B, EPCAM , (...)

View the complete list with 125 more genes
Specificity
1 %
Genes
100 %
Hereditary Renal Cancer Panel.

By Blueprint Genetics (Finland).

SDHB, SDHC, SDHD, SMARCA4, SMARCB1, EPCAM, TP53, TSC1, TSC2, VHL, WT1, CDC73, DICER1, CDKN1C, FLCN, DIS3L2, FH, GPC3, MET, MLH1 , (...)

View the complete list with 6 more genes
Specificity
4 %
Genes
100 %

You can get up to -3 more panels with our dedicated tool

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Sources and references

You can check the following sources for additional information.

OMIM Genetic Syndrome Finder

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