Colorectal Cancer, Hereditary Nonpolyposis, Type 6; Hnpcc6

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

Colorectal Cancer, Hereditary Nonpolyposis, Type 6; Hnpcc6 Is also known as colon cancer, hereditary nonpolyposis, type 6.

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.

Colorectal Cancer, Hereditary Nonpolyposis, Type 6; Hnpcc6 Recommended genes panels

Panel Name, Specifity and genes Tested/covered
NGS Aortic Dysfunction or Dilation and Related Disorders Panel. By Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center (United States). SKI, TGFB2, TGFBR1, TGFBR2, ACTA2, SLC2A10, CBS, COL3A1, COL5A1, COL5A2, ELN, FBLN5, FBN1, FBN2, SMAD3, MYH11, MYLK, NOTCH1, PLOD1 Specificity 6 % Genes 100 %
NGS Connective Tissue Disorders Panel. By Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center (United States). SKI, TGFB2, TGFBR1, TGFBR2, TNXB, ACTA2, SLC2A10, CBS, ACVR1, ATP6V0A2, FKBP14, SLC39A13, ADAMTS2, COL11A1, COL1A2, COL3A1, COL5A1, COL5A2, ZNF469, CHST14 , (...) View the complete list with 13 more genes Panel complete gene list SKI, TGFB2, TGFBR1, TGFBR2, TNXB, ACTA2, SLC2A10, CBS, ACVR1, ATP6V0A2, FKBP14, SLC39A13, ADAMTS2, COL11A1, COL1A2, COL3A1, COL5A1, COL5A2, ZNF469, CHST14, ELN, FBLN5, FBN1, FBN2, ABCC6, SMAD3, MYH11, MYLK, NOTCH1, ATP7A, PKD2, PLOD1, PRDM5 Close Specificity 4 % Genes 100 %
Loeys-Dietz syndrome type 2B. By Center for Human Genetics, Inc (United States). TGFBR2 Specificity 100 % Genes 100 %
Thoracic Aortic Aneurysms and Aortic Dissections (TGFBR1/2). By Center for Human Genetics, Inc (United States). TGFBR1, TGFBR2 Specificity 50 % Genes 100 %
Loeys-Dietz Syndrome (TGFßR1, TGFßR2, SMAD3, and TGFß2). By Center for Human Genetics, Inc (United States). TGFB2, TGFBR1, TGFBR2, SMAD3 Specificity 25 % Genes 100 %
Familial Aortic Aneurysms. By Center for Human Genetics, Inc (United States). TGFB2, TGFBR1, TGFBR2, ACTA2, SMAD3, MYH11, MYLK, PRKG1 Specificity 13 % Genes 100 %
Connective Tissue Disorders 22-gene panel. By Center for Human Genetics, Inc (United States). TGFB2, TGFBR1, TGFBR2, TGFBR3, ACTA2, NTM, COL11A1, COL11A2, COL1A2, COL3A1, COL5A1, COL5A2, FBN1, FBN2, FLNA, SMAD3, MYH11, MYLK, NOTCH1, PRKG1 Specificity 5 % Genes 100 %
Marfan Syndrome Type 2. By Johns Hopkins DNA Diagnostic Laboratory Johns Hopkins Hospital (United States). TGFBR2 Specificity 100 % Genes 100 %

Sources and references

You can check the following sources for additional information.

MESH OMIM Rare Disease Symptoms Checker

If you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like ECTODERMAL DYSPLASIA, ANHIDROTIC, WITH T-CELL IMMUNODEFICIENCY, AUTOSOMAL DOMINANT FECHTNER SYNDROME; FTNS DANON DISEASE LATERAL MENINGOCELE SYNDROME; LMNS WILSON DISEASE EPISODIC PAIN SYNDROME, FAMILIAL, 1; FEPS1 HOLOPROSENCEPHALY 7; HPE7