All diseases

OMIM ID
120435
OMIM term:
LYNCH SYNDROME I
Alternative terms:
COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 1; HNPCC1
COLON CANCER, FAMILIAL NONPOLYPOSIS, TYPE 1; FCC1
COCA1 LYNCH SYNDROME II, INCLUDED
(∗) Location:
2p21  
(†) Associated OMIM genes:
MSH2  
(‡) Associated MGI genes:
Msh2  

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