NRAS, NRAS proto-oncogene, GTPase, 4893

N. diseases: 611; N. variants: 17
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.800 GeneticVariation disease UNIPROT
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.800 Biomarker disease GENOMICS_ENGLAND
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.800 CausalMutation disease CLINVAR
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.800 Biomarker disease CTD_human
CUI: C0349639
Disease: Juvenile Myelomonocytic Leukemia
Juvenile Myelomonocytic Leukemia 		0.800 Biomarker disease HPO
CUI: C0028326
Disease: Noonan Syndrome
Noonan Syndrome 		0.780 Biomarker disease GENOMICS_ENGLAND
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 CausalMutation disease CGI
CUI: C0025202
Disease: melanoma
melanoma 		0.700 Biomarker disease HPO
CUI: C0025202
Disease: melanoma
melanoma 		0.700 CausalMutation disease CGI
CUI: C1842036
Disease: GIANT PIGMENTED HAIRY NEVUS
GIANT PIGMENTED HAIRY NEVUS 		0.700 CausalMutation disease CLINVAR
CUI: C1842036
Disease: GIANT PIGMENTED HAIRY NEVUS
GIANT PIGMENTED HAIRY NEVUS 		0.700 Biomarker disease CTD_human
CUI: C1842036
Disease: GIANT PIGMENTED HAIRY NEVUS
GIANT PIGMENTED HAIRY NEVUS 		0.700 Biomarker disease HPO
CUI: C2674723
Disease: RAS-ASSOCIATED AUTOIMMUNE LEUKOPROLIFERATIVE DISORDER
RAS-ASSOCIATED AUTOIMMUNE LEUKOPROLIFERATIVE DISORDER 		0.700 CausalMutation disease CLINVAR
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
CUI: C0265329
Disease: Organoid Nevus Phakomatosis
Organoid Nevus Phakomatosis 		0.600 CausalMutation disease CLINVAR
CUI: C0265329
Disease: Organoid Nevus Phakomatosis
Organoid Nevus Phakomatosis 		0.600 Biomarker disease CTD_human
CUI: C0334082
Disease: NEVUS, EPIDERMAL (disorder)
NEVUS, EPIDERMAL (disorder) 		0.600 Biomarker disease CTD_human
CUI: C0334082
Disease: NEVUS, EPIDERMAL (disorder)
NEVUS, EPIDERMAL (disorder) 		0.600 CausalMutation disease CLINVAR
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
CUI: C4552097
Disease: Nevus Sebaceus of Jadassohn
Nevus Sebaceus of Jadassohn 		0.600 Biomarker disease GENOMICS_ENGLAND
CUI: C4552097
Disease: Nevus Sebaceus of Jadassohn
Nevus Sebaceus of Jadassohn 		0.600 CausalMutation disease CLINVAR
CUI: C4552097
Disease: Nevus Sebaceus of Jadassohn
Nevus Sebaceus of Jadassohn 		0.600 Biomarker disease HPO
CUI: C4552097
Disease: Nevus Sebaceus of Jadassohn
Nevus Sebaceus of Jadassohn 		0.600 Biomarker disease CTD_human