NRAS, NRAS proto-oncogene, GTPase, 4893

N. diseases: 611; N. variants: 17
Disease: Neurocutaneous melanosis ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0544862
Disease: Neurocutaneous melanosis
Neurocutaneous melanosis 		0.600 GeneticVariation phenotype UNIPROT Multiple congenital melanocytic nevi and neurocutaneous melanosis are caused by postzygotic mutations in codon 61 of NRAS. 23392294 2013
CUI: C0544862
Disease: Neurocutaneous melanosis
Neurocutaneous melanosis 		0.600 Biomarker phenotype CTD_human
CUI: C0544862
Disease: Neurocutaneous melanosis
Neurocutaneous melanosis 		0.600 CausalMutation phenotype CLINVAR