OAS1, 2'-5'-oligoadenylate synthetase 1, 4938

N. diseases: 72; N. variants: 11
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: C0002871
Disease: Anemia
Anemia
disease Hemic and Lymphatic Diseases Disease or Syndrome 847 94 0.010 None 1.000 1 2012 2012
CUI: C0016382
Disease: Flushing
Flushing
phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 83 9 0.010 None 1.000 1 2019 2019
CUI: C0023890
Disease: Liver Cirrhosis
Liver Cirrhosis
disease Pathological Conditions, Signs and Symptoms; Digestive System Diseases Disease or Syndrome 1182 189 0.010 None 1.000 1 2009 2009
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma
disease Neoplasms; Male Urogenital Diseases Neoplastic Process 4388 1168 0.020 None 1.000 2 2 2011 2012
CUI: C0751583
Disease: Encephalitis, West Nile Fever
Encephalitis, West Nile Fever
disease Infections; Nervous System Diseases Disease or Syndrome 4 0.020 None 1.000 2 2010 2011
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
disease Neoplasms; Male Urogenital Diseases Neoplastic Process 4502 1082 0.020 None 1.000 2 2 2011 2012
CUI: C0011311
Disease: Dengue Fever
Dengue Fever
disease Infections Disease or Syndrome 360 39 0.020 None 0.500 2 2 2009 2013
CUI: C1175175
Disease: Severe Acute Respiratory Syndrome
Severe Acute Respiratory Syndrome
disease Infections; Respiratory Tract Diseases Disease or Syndrome 117 1 0.020 None 1.000 2 2005 2006
CUI: C0018572
Disease: Hand, Foot and Mouth Disease
Hand, Foot and Mouth Disease
disease Infections Disease or Syndrome 63 13 0.020 None 1.000 2 1 2014 2015
CUI: C0043124
Disease: West Nile Fever
West Nile Fever
disease Infections; Nervous System Diseases Disease or Syndrome 79 0.020 None 1.000 2 2010 2011
CUI: C0019163
Disease: Hepatitis B
Hepatitis B
disease Digestive System Diseases; Infections Disease or Syndrome 1449 519 0.020 None 1.000 2 1 2017 2018
CUI: C1527336
Disease: Sjogren's Syndrome
Sjogren's Syndrome
disease Eye Diseases; Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases; Stomatognathic Diseases Disease or Syndrome 481 47 0.030 None 1.000 3 1 2017 2018
CUI: C0239946
Disease: Fibrosis, Liver
Fibrosis, Liver
disease Pathological Conditions, Signs and Symptoms; Digestive System Diseases Disease or Syndrome 1179 64 0.030 None 1.000 3 2 2009 2017
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
disease Immune System Diseases; Nervous System Diseases Disease or Syndrome 1800 1022 0.040 None 1.000 4 2 2006 2012
CUI: C3714514
Disease: Infection
Infection
group Infections Pathologic Function 491 0.040 None 1.000 4 2002 2005
CUI: C1096184
Disease: West Nile viral infection
West Nile viral infection
disease Infections; Nervous System Diseases Disease or Syndrome 164 2 0.040 None 0.750 4 1 2008 2019
Diabetes Mellitus, Insulin-Dependent
disease Nutritional and Metabolic Diseases; Immune System Diseases; Endocrine System Diseases Disease or Syndrome 1675 954 0.060 None 1.000 6 1 2005 2009
CUI: C0019196
Disease: Hepatitis C
Hepatitis C
disease Digestive System Diseases; Infections Disease or Syndrome 1768 347 0.100 None 1.000 14 3 2003 2018
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement
phenotype Laboratory Procedure 1156 2575 0.100 None 1.000 2 2 2018 2018
Serum gamma-glutamyl transferase measurement
phenotype Laboratory Procedure 54 108 0.100 None 1.000 1 1 2011 2011
CUI: C0202239
Disease: Uric acid measurement (procedure)
Uric acid measurement (procedure)
phenotype Laboratory Procedure 264 1463 0.100 None 1.000 1 1 2019 2019
CUI: C0200635
Disease: Lymphocyte Count measurement
Lymphocyte Count measurement
phenotype Laboratory Procedure 338 456 0.100 None 1.000 1 1 2012 2012
Gamma glutamyl transferase measurement
phenotype Laboratory Procedure 5 7 0.100 None 1.000 1 1 2011 2011
CUI: C0010200
Disease: Coughing
Coughing
phenotype Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases Sign or Symptom 235 16 0.100 None 0
CUI: C0034642
Disease: Rales
Rales
phenotype Pathological Conditions, Signs and Symptoms Finding 23 0.100 None 0