NRAS, NRAS proto-oncogene, GTPase, 4893

N. diseases: 611; N. variants: 17
Disease: Noonan Syndrome 6 ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C2750732
Disease: Noonan Syndrome 6
Noonan Syndrome 6 		0.700 Biomarker disease GENOMICS_ENGLAND The RASopathies. 23875798 2013
CUI: C2750732
Disease: Noonan Syndrome 6
Noonan Syndrome 6 		0.700 Biomarker disease GENOMICS_ENGLAND The RASopathies. 23875798 2013
CUI: C2750732
Disease: Noonan Syndrome 6
Noonan Syndrome 6 		0.700 Biomarker disease GENOMICS_ENGLAND A restricted spectrum of NRAS mutations causes Noonan syndrome. 19966803 2010
CUI: C2750732
Disease: Noonan Syndrome 6
Noonan Syndrome 6 		0.700 GeneticVariation disease UNIPROT A restricted spectrum of NRAS mutations causes Noonan syndrome. 19966803 2010
CUI: C2750732
Disease: Noonan Syndrome 6
Noonan Syndrome 6 		0.700 Biomarker disease GENOMICS_ENGLAND Germ-line mutation of the NRAS gene may be responsible for the development of juvenile myelomonocytic leukaemia. 19775298 2009
CUI: C2750732
Disease: Noonan Syndrome 6
Noonan Syndrome 6 		0.700 Biomarker disease CTD_human
CUI: C2750732
Disease: Noonan Syndrome 6
Noonan Syndrome 6 		0.700 CausalMutation disease CLINVAR