Source: CLINGEN

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4893
Gene Symbol: NRAS
NRAS
CUI: C0175704
Disease: LEOPARD Syndrome
LEOPARD Syndrome 		0.300 Biomarker CLINGEN Mutation in NRAS in familial Noonan syndrome--case report and review of the literature. 26467218

2015
Entrez Id: 4893
Gene Symbol: NRAS
NRAS
CUI: C0175704
Disease: LEOPARD Syndrome
LEOPARD Syndrome 		0.300 Biomarker CLINGEN The RASopathies. 23875798

2013
Entrez Id: 4893
Gene Symbol: NRAS
NRAS
CUI: C0175704
Disease: LEOPARD Syndrome
LEOPARD Syndrome 		0.300 Biomarker CLINGEN Constitutional NRAS mutations are rare among patients with Noonan syndrome or juvenile myelomonocytic leukemia. 22887781

2012
Entrez Id: 4893
Gene Symbol: NRAS
NRAS
CUI: C0175704
Disease: LEOPARD Syndrome
LEOPARD Syndrome 		0.300 Biomarker CLINGEN Germ-line mutation of the NRAS gene may be responsible for the development of juvenile myelomonocytic leukaemia. 19775298

2009