SIRT3, sirtuin 3, 23410

N. diseases: 227; 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: C1269955
Disease: Tumor Cell Invasion
Tumor Cell Invasion
phenotype Neoplastic Process 6626 169 0.060 None 1.000 6 2014 2020
CUI: C0856169
Disease: Endothelial dysfunction
Endothelial dysfunction
phenotype Disease or Syndrome 716 25 0.030 None 1.000 3 2017 2019
CUI: C1397307
Disease: Cardiac fibrosis
Cardiac fibrosis
disease Disease or Syndrome 297 3 0.020 None 1.000 2 2017 2019
CUI: C2242776
Disease: Plexiform leiomyoma
Plexiform leiomyoma
disease Neoplastic Process 41 103 0.100 None 1.000 2 2 2018 2019
CUI: C4020732
Disease: Mitochondrial abnormalities
Mitochondrial abnormalities
disease Anatomical Abnormality 83 20 0.020 None 1.000 2 2017 2017
CUI: C0236734
Disease: Caffeine related disorders
Caffeine related disorders
group Mental or Behavioral Dysfunction 360 56 0.010 None 1.000 1 2018 2018
CUI: C0263009
Disease: Sclerosis of the skin
Sclerosis of the skin
disease Disease or Syndrome 22 0.010 None 1.000 1 2016 2016
CUI: C0340757
Disease: Inferior vena cava stenosis
Inferior vena cava stenosis
disease Disease or Syndrome 3 0.010 None 1.000 1 2017 2017
CUI: C1262048
Disease: Glial scar
Glial scar
phenotype Acquired Abnormality 51 0.010 None 1.000 1 2017 2017
Metastasis from malignant tumor of prostate
disease Neoplastic Process 342 18 0.010 None < 0.001 1 2018 2018
CUI: C1561826
Disease: Overweight and obesity
Overweight and obesity
disease Disease or Syndrome 81 29 0.010 None 1.000 1 2019 2019
CUI: C1868702
Disease: Diabetic keratopathy
Diabetic keratopathy
disease Disease or Syndrome 5 0.010 None 1.000 1 2019 2019
CUI: C1969372
Disease: Tubulointerstitial fibrosis
Tubulointerstitial fibrosis
phenotype Disease or Syndrome 328 0.010 None 1.000 1 2018 2018
FATTY LIVER DISEASE, NONALCOHOLIC, SUSCEPTIBILITY TO, 1
disease Finding 63 2 0.200 None 1.000 1 2012 2012
LIVER DISEASE, ALCOHOLIC, SUSCEPTIBILITY TO, 1
phenotype Finding 63 0.200 None 1.000 1 2012 2012
Long chain/very long chain acyl CoA dehydrogenase deficiency
disease Disease or Syndrome 1 0.010 None 1.000 1 2018 2018
FATTY LIVER DISEASE, NONALCOHOLIC, SUSCEPTIBILITY TO, 2
phenotype Finding 63 0.200 None 1.000 1 2012 2012
CUI: C3160887
Disease: Node-positive breast cancer
Node-positive breast cancer
disease Neoplastic Process 40 3 0.010 None 1.000 1 2006 2006
CUI: C3642346
Disease: Luminal B Breast Carcinoma
Luminal B Breast Carcinoma
disease Neoplastic Process 103 7 0.010 None 1.000 1 2016 2016
CUI: C3825201
Disease: Mitochondrial pathology
Mitochondrial pathology
phenotype Disease or Syndrome 20 6 0.010 None 1.000 1 2018 2018
CUI: C4049446
Disease: Neointimal hyperplasia
Neointimal hyperplasia
disease Disease or Syndrome 198 0.010 None 1.000 1 2020 2020
Neutrophil extracellular trap formation
disease Disease or Syndrome 55 0.010 None 1.000 1 2018 2018
Heart failure with preserved ejection fraction [HFpEF]
disease Disease or Syndrome 89 4 0.010 None 1.000 1 2019 2019
CUI: C4529962
Disease: Fatty Liver Disease
Fatty Liver Disease
disease Disease or Syndrome 741 81 0.010 None 1.000 1 2017 2017
Malignant neoplasm of colon and/or rectum
disease Neoplastic Process 3669 502 0.010 None 1.000 1 2018 2018