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: C0273115
Disease: Lung Injury
Lung Injury 		disease Respiratory Tract Diseases; Wounds and Injuries Injury or Poisoning 30 0.300 None 1.000 1 2014 2014
CUI: C0235272
Disease: Retinal damage
Retinal damage 		phenotype Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases; Wounds and Injuries Disease or Syndrome 32 1 0.010 None 1.000 1 2018 2018
CUI: C0270952
Disease: Muscular Dystrophy, Oculopharyngeal
Muscular Dystrophy, Oculopharyngeal 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases Disease or Syndrome 33 4 0.010 None 1.000 1 2008 2008
CUI: C0852733
Disease: Completed Suicide
Completed Suicide 		phenotype Mental or Behavioral Dysfunction 33 33 0.010 None < 0.001 1 2019 2019
CUI: C1955934
Disease: Trichothiodystrophy Syndromes
Trichothiodystrophy Syndromes 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases Disease or Syndrome 33 15 0.010 None 1.000 1 2014 2014
CUI: C2350344
Disease: Chronic Lung Injury
Chronic Lung Injury 		disease Respiratory Tract Diseases; Wounds and Injuries Disease or Syndrome 33 0.300 None 1.000 1 2014 2014
CUI: C0877009
Disease: Muscle fibrosis
Muscle fibrosis 		phenotype Sign or Symptom 34 0.010 None 1.000 1 2019 2019
CUI: C0752130
Disease: Spinal Cord Ischemia
Spinal Cord Ischemia 		disease Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 35 3 0.020 None 1.000 2 2019 2019
CUI: C0160390
Disease: Injury of liver
Injury of liver 		disease Digestive System Diseases; Wounds and Injuries Injury or Poisoning 36 0.200 None 1.000 1 2014 2014
CUI: C0178264
Disease: Inflammatory disease of the central nervous system
Inflammatory disease of the central nervous system 		group Nervous System Diseases Disease or Syndrome 36 0.010 None 1.000 1 2019 2019
CUI: C1858556
Disease: OVERLAP CONNECTIVE TISSUE DISEASE
OVERLAP CONNECTIVE TISSUE DISEASE 		disease Eye Diseases; Skin and Connective Tissue Diseases; Cardiovascular Diseases Disease or Syndrome 36 31 0.010 None < 0.001 1 2017 2017
CUI: C4324374
Disease: Renal tubular injury
Renal tubular injury 		disease Disease or Syndrome 36 1 0.010 None 1.000 1 2018 2018
CUI: C0023486
Disease: Prolymphocytic Leukemia
Prolymphocytic Leukemia 		disease Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases Neoplastic Process 37 2 0.010 None 1.000 1 2016 2016
CUI: C0221238
Disease: Mesangial proliferative glomerulonephritis
Mesangial proliferative glomerulonephritis 		disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 37 0.010 None 1.000 1 2018 2018
CUI: C0740903
Disease: allergic symptom
allergic symptom 		phenotype Sign or Symptom 37 2 0.010 None 1.000 1 2018 2018
CUI: C0206172
Disease: Diabetic Foot
Diabetic Foot 		disease Skin and Connective Tissue Diseases; Endocrine System Diseases; Cardiovascular Diseases Disease or Syndrome 39 13 0.010 None 1.000 1 2 2018 2018
CUI: C0265004
Disease: Dilatation of aorta
Dilatation of aorta 		phenotype Cardiovascular Diseases Disease or Syndrome 39 2 0.010 None 1.000 1 2016 2016
CUI: C0750977
Disease: Recurrent Brain Neoplasm
Recurrent Brain Neoplasm 		disease Neoplasms; Nervous System Diseases Neoplastic Process 39 0.300 None 1.000 1 2012 2012
CUI: C0751733
Disease: Degenerative Diseases, Spinal Cord
Degenerative Diseases, Spinal Cord 		group Nervous System Diseases Disease or Syndrome 40 0.300 None 1.000 2 2007 2007
CUI: C0149896
Disease: Primary gout
Primary gout 		disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases Disease or Syndrome 40 5 0.010 None 1.000 1 2019 2019
CUI: C0238052
Disease: Xanthomatosis, Cerebrotendinous
Xanthomatosis, Cerebrotendinous 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 40 71 0.010 None 1.000 1 2019 2019
CUI: C0031029
Disease: Periapical Granuloma
Periapical Granuloma 		disease Stomatognathic Diseases Disease or Syndrome 41 0.020 None 1.000 2 2018 2018
CUI: C0036982
Disease: Shock, Hemorrhagic
Shock, Hemorrhagic 		phenotype Pathological Conditions, Signs and Symptoms Pathologic Function 41 0.200 None 1.000 2 2011 2012
CUI: C0021171
Disease: Bloch Sulzberger syndrome
Bloch Sulzberger syndrome 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases Disease or Syndrome 41 10 0.010 None 1.000 1 2017 2017
CUI: C0496899
Disease: Benign neoplasm of brain, unspecified
Benign neoplasm of brain, unspecified 		disease Neoplasms; Nervous System Diseases Neoplastic Process 41 0.300 None 1.000 1 2012 2012