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MIM:614331 - COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 6; HNPCC6
Xenbase Genes: tgfbr2, tgfbr2l
Human Disease Resource: MIM
MONDO:0005835 - Lynch syndrome |
MONDO:0013695 - colorectal cancer, hereditary nonpolyposis, type 6 |
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MONDO:0005835 - Lynch syndrome |
MONDO:0013695 - colorectal cancer, hereditary nonpolyposis, type 6 |