SIRT1, sirtuin 1, 23411

N. diseases: 675; N. variants: 21
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: C0392662
Disease: Angiostrongyliasis
Angiostrongyliasis
disease Infections Disease or Syndrome 2 0.010 None 1.000 1 2017 2017
CUI: C4316792
Disease: Angiostrongylus Infections
Angiostrongylus Infections
disease Infections Disease or Syndrome 2 0.010 None 1.000 1 2017 2017
CUI: C0556346
Disease: Binge Drinking
Binge Drinking
phenotype Chemically-Induced Disorders; Mental Disorders; Behavior and Behavior Mechanisms Individual Behavior 3 0.200 None 1.000 1 2014 2014
CUI: C0744474
Disease: Gram-positive bacteremia
Gram-positive bacteremia
disease Disease or Syndrome 3 0.010 None 1.000 1 2013 2013
Anterior Cerebral Circulation Infarction
phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 5 0.300 None 1.000 1 2012 2012
Anterior Circulation Brain Infarction
phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 5 0.300 None 1.000 1 2012 2012
Brain Infarction, Posterior Circulation
phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 5 0.300 None 1.000 1 2012 2012
CUI: C0751954
Disease: Venous Infarction, Brain
Venous Infarction, Brain
phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 5 0.300 None 1.000 1 2012 2012
CUI: C0919532
Disease: Genomic Instability
Genomic Instability
phenotype Pathological Conditions, Signs and Symptoms Cell or Molecular Dysfunction 5 0.300 None 1.000 1 2012 2012
CUI: C0033587
Disease: Prosthesis Loosening
Prosthesis Loosening
disease Pathological Conditions, Signs and Symptoms Disease or Syndrome 6 0.020 None 1.000 2 2017 2017
CUI: C1850625
Disease: Native American myopathy
Native American myopathy
disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases; Stomatognathic Diseases Disease or Syndrome 6 3 0.020 None 1.000 2 2013 2017
Proliferative diabetic retinopathy - quiescent
disease Disease or Syndrome 6 0.010 None 1.000 1 2019 2019
CUI: C1281373
Disease: Intercritical gout
Intercritical gout
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases Disease or Syndrome 6 0.010 None 1.000 1 2019 2019
CUI: C0019296
Disease: Inguinal Hernia, Indirect
Inguinal Hernia, Indirect
disease Pathological Conditions, Signs and Symptoms Disease or Syndrome 7 2 0.010 None 1.000 1 2 2014 2014
CUI: C4317126
Disease: Niacin deficiency
Niacin deficiency
disease Nutritional and Metabolic Diseases Disease or Syndrome 7 1 0.010 None 1.000 1 2009 2009
CUI: C0011304
Disease: Demyelination
Demyelination
phenotype Nervous System Diseases Pathologic Function 9 0.300 None 1.000 1 2013 2013
CUI: C0848255
Disease: female puberty
female puberty
phenotype Sign or Symptom 9 0.010 None 1.000 1 2018 2018
Clinically Isolated Syndrome, CNS Demyelinating
disease Nervous System Diseases Disease or Syndrome 9 0.300 None 1.000 1 2013 2013
Cervical Intraepithelial Neoplasia Grade 2/3
disease Neoplastic Process 9 0.010 None 1.000 1 2017 2017
CUI: C0234544
Disease: Todd Paralysis
Todd Paralysis
phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases Sign or Symptom 10 0.300 None 1.000 1 2013 2013
CUI: C0581377
Disease: Decompensated cardiac failure
Decompensated cardiac failure
disease Cardiovascular Diseases Disease or Syndrome 12 0.010 None 1.000 1 2015 2015
CUI: C0920715
Disease: Myocardial hypoxia
Myocardial hypoxia
disease Disease or Syndrome 13 0.010 None 1.000 1 2019 2019
Ceroid lipofuscinosis, neuronal 1, infantile
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases Disease or Syndrome 14 1 0.300 None 1.000 1 2011 2011
CUI: C0238669
Disease: Aortic root dilatation
Aortic root dilatation
disease Cardiovascular Diseases Anatomical Abnormality 15 0.010 None 1.000 1 2016 2016
Benign Paroxysmal Positional Vertigo
disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Otorhinolaryngologic Diseases Disease or Syndrome 16 1 0.020 None 1.000 2 2015 2016