Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 6
0.600 CausalMutation disease CLINVAR A syndrome of altered cardiovascular, craniofacial, neurocognitive and skeletal development caused by mutations in TGFBR1 or TGFBR2. 15731757 2005
COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 6
0.600 CausalMutation disease CLINVAR Mutational inactivation of transforming growth factor beta receptor type II in microsatellite stable colon cancers. 9927040 1999
COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 6
0.600 GeneticVariation disease UNIPROT HNPCC associated with germline mutation in the TGF-beta type II receptor gene. 9590282 1998
COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 6
0.600 CausalMutation disease CLINVAR Inactivation of the type II TGF-beta receptor in colon cancer cells with microsatellite instability. 7761852 1995
COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 6
0.600 Biomarker disease CTD_human