Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 5979
Gene Symbol: RET
RET
Multiple Endocrine Neoplasia Type 2b
1.000 CausalMutation CLINVAR Clinical presentations and RET protooncogene mutations in seven multiple endocrine neoplasia type 2 kindreds. 8909322

1996

Entrez Id: 5979
Gene Symbol: RET
RET
Multiple Endocrine Neoplasia Type 2b
1.000 CausalMutation CLINVAR Multiple endocrine neoplasia type 2B (mucosal neuroma syndrome, Wagenmann-Froboese syndrome). 8880581

1996

Entrez Id: 5979
Gene Symbol: RET
RET
Multiple Endocrine Neoplasia Type 2b
1.000 CausalMutation CLINVAR Activation of RET as a dominant transforming gene by germline mutations of MEN2A and MEN2B. 7824936

1995

Entrez Id: 5979
Gene Symbol: RET
RET
Multiple Endocrine Neoplasia Type 2b
1.000 GeneticVariation CLINVAR RET activation by germline MEN2A and MEN2B mutations. 8570194

1995

Entrez Id: 5979
Gene Symbol: RET
RET
Multiple Endocrine Neoplasia Type 2b
1.000 CausalMutation CLINVAR Germline RET mutations in MEN 2A and FMTC and their detection by simple DNA diagnostic tests. 7915165

1994

Entrez Id: 5979
Gene Symbol: RET
RET
Multiple Endocrine Neoplasia Type 2b
1.000 CausalMutation CLINVAR A mutation in the RET proto-oncogene associated with multiple endocrine neoplasia type 2B and sporadic medullary thyroid carcinoma. 7906866

1994

Entrez Id: 5979
Gene Symbol: RET
RET
Multiple Endocrine Neoplasia Type 2b
1.000 CausalMutation CLINVAR Sequence analysis of germ-line DNA from MEN 2B patients revealed the existence of the same point mutation in the RET protooncogene in 34 unrelated individuals. 7906417

1994

Entrez Id: 5979
Gene Symbol: RET
RET
Multiple Endocrine Neoplasia Type 2b
1.000 CausalMutation CLINVAR RET proto-oncogene mutations in French MEN 2A and FMTC families. 7874109

1994