NRAS, NRAS proto-oncogene, GTPase, 4893

N. diseases: 611; N. variants: 17
Source: ALL
Disease Type Disease Class Semantic Type N. genes d N. SNPs d Score gda EL gda EI gda N. PMIDs N. SNPs gda First Ref. Last Ref.
CUI: C0023441
Disease: Leukemia, Experimental
Leukemia, Experimental
disease Neoplasms Experimental Model of Disease 1 0.200 None 1.000 1 1997 1997
CUI: C0349539
Disease: Malignant melanoma of rectum
Malignant melanoma of rectum
disease Neoplastic Process 1 0.010 None 1.000 1 2012 2012
CUI: C0544862
Disease: Neurocutaneous melanosis
Neurocutaneous melanosis
phenotype Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Nervous System Diseases Pathologic Function 1 2 0.600 None 1.000 1 2 2013 2013
childhood acute myeloid leukemia/other myeloid malignancies
disease Neoplasms Neoplastic Process 1 0.010 None 1.000 1 1991 1991
CUI: C1334691
Disease: Melanomatosis
Melanomatosis
disease Neoplasms Neoplastic Process 1 1 0.010 None 1.000 1 1 2016 2016
Spondylocostal Dysostosis with Anal Atresia and Urogenital Anomalies
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Female Urogenital Diseases and Pregnancy Complications; Musculoskeletal Diseases; Male Urogenital Diseases Disease or Syndrome; Congenital Abnormality 1 1 0.010 None 1.000 1 1 2015 2015
CUI: C3805812
Disease: NEUROCUTANEOUS MELANOSIS, SOMATIC
NEUROCUTANEOUS MELANOSIS, SOMATIC
phenotype Finding 1 0.300 limited 1.000 1 2008 2008
Numerous congenital melanocytic nevi
phenotype Neoplasms Finding 1 0.100 None 0
CUI: C1332888
Disease: Central nervous system melanoma
Central nervous system melanoma
disease Neoplastic Process 2 0.040 None 0.750 4 2013 2018
CUI: C2750732
Disease: Noonan Syndrome 6
Noonan Syndrome 6
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Cardiovascular Diseases Disease or Syndrome 3 3 0.700 strong 1.000 3 3 2009 2013
CUI: C0234894
Disease: Dermatitis acneiform
Dermatitis acneiform
disease Skin and Connective Tissue Diseases Disease or Syndrome 3 0.010 None 1.000 1 2013 2013
CUI: C3161106
Disease: Pulmonary interstitial glycogenosis
Pulmonary interstitial glycogenosis
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Respiratory Tract Diseases Disease or Syndrome 3 0.010 None 1.000 1 2014 2014
CUI: C4020895
Disease: Genitourinary dysplasia
Genitourinary dysplasia
disease Anatomical Abnormality 3 0.010 None 1.000 1 1987 1987
CUI: C0346099
Disease: Nevus spilus
Nevus spilus
disease Neoplasms; Skin and Connective Tissue Diseases Neoplastic Process 3 0.100 None 0
CUI: C3280131
Disease: Long eyebrows
Long eyebrows
phenotype Finding 3 0.100 None 0
CUI: C2363750
Disease: MDS transformation
MDS transformation
disease Neoplastic Process 4 0.010 None 1.000 1 2007 2007
Autoimmune Lymphoproliferative Syndrome Type 1, Autosomal Dominant
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Immune System Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 4 0.300 None 1.000 1 2007 2007
Nevus, Keratinocytic, Nonepidermolytic
disease Neoplasms Neoplastic Process 4 0.300 None 0
CUI: C1842036
Disease: GIANT PIGMENTED HAIRY NEVUS
GIANT PIGMENTED HAIRY NEVUS
disease Neoplasms; Skin and Connective Tissue Diseases Neoplastic Process 5 6 0.700 None 1.000 3 3 2009 2014
CUI: C1306726
Disease: Congenital naevus
Congenital naevus
disease Neoplastic Process 5 1 0.010 None 1.000 1 1 2016 2016
CUI: C1511104
Disease: Benign Struma Ovarii
Benign Struma Ovarii
disease Neoplasms Neoplastic Process 5 0.010 None 1.000 1 2007 2007
CUI: C1854978
Disease: Monosomy 7 of Bone Marrow
Monosomy 7 of Bone Marrow
disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Hemic and Lymphatic Diseases Disease or Syndrome 5 1 0.010 None 1.000 1 1994 1994
Inflammatory linear verrucous epidermal nevus
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Nervous System Diseases Neoplastic Process 5 0.300 None 0
CUI: C1858969
Disease: Decreased lymphocyte apoptosis
Decreased lymphocyte apoptosis
phenotype Finding 5 0.100 None 0
CUI: C2749369
Disease: Prominence of the premaxilla
Prominence of the premaxilla
phenotype Finding 5 1 0.100 None 0