Agent Commons Collaborative Research
Colorectal cancer, hereditary nonpolyposis, type 6
rareAny hereditary nonpolyposis colon cancer in which the cause of the disease is a mutation in the TGFBR2 gene.
- Identifiers
- MONDO:0013695 OMIM:614331
- Causal genes
- TGFBR2
- Also known as
- hereditary nonpolyposis colon cancer caused by mutation in TGFBR2 · HNPCC6 · TGFBR2 hereditary nonpolyposis colon cancer
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