PPARGC1B, PPARG coactivator 1 beta, 133522

N. diseases: 102; N. variants: 16
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: C3547188
Disease: response to fenofibrate
response to fenofibrate
phenotype Cell Function 4 5 0.100 None 1.000 1 1 2012 2012
CUI: C0264122
Disease: Atrophy, Disuse
Atrophy, Disuse
disease Musculoskeletal Diseases; Nervous System Diseases Disease or Syndrome 16 0.020 None 1.000 2 2012 2017
Benign Paroxysmal Positional Vertigo
disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Otorhinolaryngologic Diseases Disease or Syndrome 16 1 0.010 None 1.000 1 2016 2016
CUI: C1706412
Disease: Lipidemias
Lipidemias
phenotype Nutritional and Metabolic Diseases Finding 18 0.300 None 1.000 1 2007 2007
CUI: C0025209
Disease: Melanosis
Melanosis
disease Skin and Connective Tissue Diseases Disease or Syndrome 26 23 0.100 None 1.000 1 1 2018 2018
Left ventricular diastolic dysfunction
disease Cardiovascular Diseases Disease or Syndrome 31 1 0.010 None 1.000 1 2019 2019
Malignant melanoma of skin of upper limb
disease Neoplasms; Skin and Connective Tissue Diseases Neoplastic Process 32 42 0.100 None 1.000 1 1 2018 2018
Malignant melanoma of skin of lower limb
disease Neoplasms; Skin and Connective Tissue Diseases Neoplastic Process 32 42 0.100 None 1.000 1 1 2018 2018
CUI: C0347950
Disease: Asthma attack
Asthma attack
disease Respiratory Tract Diseases; Immune System Diseases Disease or Syndrome 32 1 0.010 None 1.000 1 2016 2016
CUI: C0026857
Disease: Musculoskeletal Diseases
Musculoskeletal Diseases
group Musculoskeletal Diseases Disease or Syndrome 38 5 0.010 None 1.000 1 2014 2014
CUI: C0271708
Disease: Fasting Hypoglycemia
Fasting Hypoglycemia
phenotype Nutritional and Metabolic Diseases Disease or Syndrome 39 1 0.010 None 1.000 1 2004 2004
CUI: C0151798
Disease: Hepatic necrosis
Hepatic necrosis
phenotype Digestive System Diseases Disease or Syndrome 44 0.010 None 1.000 1 2019 2019
CUI: C0856727
Disease: Cholesterol gallstones
Cholesterol gallstones
disease Digestive System Diseases Disease or Syndrome 51 12 0.010 None 1.000 1 2006 2006
CUI: C0406208
Disease: Suntan
Suntan
phenotype Organ or Tissue Function 53 94 0.100 None 1.000 1 1 2018 2018
CUI: C0206710
Disease: Basal Cell Neoplasm
Basal Cell Neoplasm
disease Neoplasms Neoplastic Process 58 109 0.100 None 1.000 1 1 2019 2019
CUI: C0155765
Disease: Disease of capillaries
Disease of capillaries
group Cardiovascular Diseases Disease or Syndrome 61 5 0.010 None 1.000 1 2018 2018
CUI: C0751676
Disease: Basal Cell Cancer
Basal Cell Cancer
disease Neoplasms Neoplastic Process 64 109 0.100 None 1.000 1 1 2019 2019
CUI: C2745963
Disease: Kashin-Beck Disease
Kashin-Beck Disease
disease Musculoskeletal Diseases Disease or Syndrome 77 43 0.010 None 1.000 1 2016 2016
CUI: C0007117
Disease: Basal cell carcinoma
Basal cell carcinoma
disease Neoplasms Neoplastic Process 108 109 0.100 None 1.000 1 1 2019 2019
CUI: C0276138
Disease: Viral myocarditis
Viral myocarditis
disease Infections; Cardiovascular Diseases Disease or Syndrome 129 2 0.010 None 1.000 1 2018 2018
CUI: C3642345
Disease: Luminal A Breast Carcinoma
Luminal A Breast Carcinoma
disease Neoplastic Process 153 11 0.010 None 1.000 1 2016 2016
CUI: C0947622
Disease: Cholecystolithiasis
Cholecystolithiasis
disease Digestive System Diseases Disease or Syndrome 156 62 0.010 None 1.000 1 2006 2006
CUI: C0750952
Disease: Biliary Tract Cancer
Biliary Tract Cancer
disease Digestive System Diseases; Neoplasms Neoplastic Process 167 11 0.010 None < 0.001 1 2020 2020
CUI: C1512127
Disease: HER2 gene amplification
HER2 gene amplification
disease Disease or Syndrome 170 14 0.010 None 1.000 1 2016 2016
CUI: C0917801
Disease: Sleeplessness
Sleeplessness
phenotype Nervous System Diseases; Mental Disorders Sign or Symptom 174 30 0.010 None 1.000 1 2012 2012