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: C0085426
Disease: Gram-Positive Bacterial Infections
Gram-Positive Bacterial Infections 		group Infections Disease or Syndrome 17 1 0.010 None 1.000 1 2013 2013
CUI: C0432291
Disease: Mandibuloacral dysostosis
Mandibuloacral dysostosis 		disease Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases; Musculoskeletal Diseases Disease or Syndrome 17 16 0.010 None 1.000 1 2014 2014
CUI: C4022459
Disease: Decreased adipose tissue
Decreased adipose tissue 		phenotype Sign or Symptom 17 0.010 None 1.000 1 2018 2018
CUI: C0020564
Disease: Hypertrophy
Hypertrophy 		phenotype Pathological Conditions, Signs and Symptoms Pathologic Function 18 0.300 None 1.000 1 2013 2013
CUI: C0039503
Disease: Tendinitis
Tendinitis 		disease Musculoskeletal Diseases; Wounds and Injuries Disease or Syndrome 18 0.010 None 1.000 1 2012 2012
CUI: C4551902
Disease: Craniosynostosis, Type 1
Craniosynostosis, Type 1 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases Disease or Syndrome 18 28 0.010 None 1.000 1 7 2019 2019
CUI: C0796135
Disease: Renpenning syndrome 1
Renpenning syndrome 1 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Disease or Syndrome 19 5 0.010 None 1.000 1 2010 2010
CUI: C0085696
Disease: Chronic prostatitis
Chronic prostatitis 		disease Male Urogenital Diseases Disease or Syndrome 20 1 0.010 None 1.000 1 2017 2017
CUI: C2242703
Disease: Cardio-Renal Syndrome
Cardio-Renal Syndrome 		disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Cardiovascular Diseases Disease or Syndrome 21 0.020 None 1.000 2 2018 2019
CUI: C0043020
Disease: Wallerian Degeneration
Wallerian Degeneration 		phenotype Pathological Conditions, Signs and Symptoms Cell or Molecular Dysfunction 21 0.300 None 1.000 1 2014 2014
CUI: C0233488
Disease: Feeling despair
Feeling despair 		phenotype Behavior and Behavior Mechanisms Sign or Symptom 21 3 0.010 None 1.000 1 2019 2019
CUI: C1868773
Disease: Diabetic encephalopathy
Diabetic encephalopathy 		disease Disease or Syndrome 21 0.010 None 1.000 1 2018 2018
CUI: C0011876
Disease: Cataract due to diabetes mellitus
Cataract due to diabetes mellitus 		disease Eye Diseases Disease or Syndrome 22 0.020 None 1.000 2 2017 2018
CUI: C0268281
Disease: Infantile neuronal ceroid lipofuscinosis
Infantile neuronal ceroid lipofuscinosis 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases Disease or Syndrome 22 4 0.010 None 1.000 1 2011 2011
CUI: C0577573
Disease: Mass of body region
Mass of body region 		phenotype Sign or Symptom 22 0.010 None 1.000 1 2019 2019
CUI: C1516061
Disease: Astler-Coller B1 Rectal Carcinoma
Astler-Coller B1 Rectal Carcinoma 		disease Neoplastic Process 22 1 0.010 None 1.000 1 2018 2018
CUI: C0017920
Disease: Glycogen Storage Disease Type I
Glycogen Storage Disease Type I 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 24 33 0.010 None 1.000 1 2018 2018
CUI: C0236848
Disease: Age-related cognitive decline
Age-related cognitive decline 		disease Mental Disorders Mental or Behavioral Dysfunction 24 3 0.010 None 1.000 1 2018 2018
CUI: C1963961
Disease: Testosterone deficiency
Testosterone deficiency 		disease Disease or Syndrome 24 1 0.010 None 1.000 1 2012 2012
CUI: C0282528
Disease: Peroxisomal Disorders
Peroxisomal Disorders 		group Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 25 1 0.010 None 1.000 1 2019 2019
CUI: C1834523
Disease: ARTHROGRYPOSIS, DISTAL, TYPE 2B
ARTHROGRYPOSIS, DISTAL, TYPE 2B 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases Disease or Syndrome 25 6 0.010 None 1.000 1 2010 2010
CUI: C0036939
Disease: Shared Paranoid Disorder
Shared Paranoid Disorder 		disease Mental Disorders Mental or Behavioral Dysfunction 27 10 0.310 None < 0.001 1 1 2011 2011
CUI: C0746556
Disease: metabolic disturbance
metabolic disturbance 		disease Disease or Syndrome 29 4 0.010 None 1.000 1 2019 2019
CUI: C1849699
Disease: Progesterone Resistance
Progesterone Resistance 		disease Female Urogenital Diseases and Pregnancy Complications Disease or Syndrome 29 0.010 None 1.000 1 2017 2017
CUI: C0025309
Disease: Meningoencephalitis
Meningoencephalitis 		disease Infections; Nervous System Diseases Disease or Syndrome 30 3 0.010 None 1.000 1 2017 2017