PPARGC1A, PPARG coactivator 1 alpha, 10891

N. diseases: 350; N. variants: 42
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: C3875179
Disease: Abnormal lipid deposits
Abnormal lipid deposits 		disease Disease or Syndrome 1 0.010 None 1.000 1 2019 2019
CUI: C0026851
Disease: Muscular Dystrophy, Animal
Muscular Dystrophy, Animal 		disease Animal Diseases Disease or Syndrome 2 0.300 None 1.000 1 2013 2013
CUI: C4087316
Disease: Muscle hypoxia
Muscle hypoxia 		disease Disease or Syndrome 3 0.010 None 1.000 1 2018 2018
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 0.010 None 1.000 1 2017 2017
CUI: C0853892
Disease: Catabolic state
Catabolic state 		phenotype Disease or Syndrome 8 0.010 None 1.000 1 2019 2019
CUI: C3830518
Disease: Diabetic embryopathy
Diabetic embryopathy 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications Disease or Syndrome 9 0.010 None 1.000 1 2017 2017
CUI: C2749515
Disease: Collapsing glomerulopathy
Collapsing glomerulopathy 		disease Disease or Syndrome 10 0.010 None 1.000 1 2018 2018
CUI: C2930930
Disease: Abdominal obesity metabolic syndrome
Abdominal obesity metabolic syndrome 		disease Nutritional and Metabolic Diseases Disease or Syndrome 10 0.200 None 1.000 1 2012 2012
CUI: C3888461
Disease: Dry age-related macular degeneration
Dry age-related macular degeneration 		phenotype Anatomical Abnormality 11 1 0.010 None 1.000 1 2019 2019
CUI: C2931673
Disease: Ceroid lipofuscinosis, neuronal 1, infantile
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: C0264122
Disease: Atrophy, Disuse
Atrophy, Disuse 		disease Musculoskeletal Diseases; Nervous System Diseases Disease or Syndrome 16 0.020 None 1.000 2 2012 2016
CUI: C0155502
Disease: Benign Paroxysmal Positional Vertigo
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: C0278506
Disease: Non-small cell lung cancer stage III
Non-small cell lung cancer stage III 		disease Neoplastic Process 16 1 0.010 None 1.000 1 2017 2017
CUI: C0268095
Disease: Keshan disease
Keshan disease 		disease Infections; Cardiovascular Diseases Disease or Syndrome 17 1 0.010 None 1.000 1 2013 2013
CUI: C0677950
Disease: Stage IV Colorectal Cancer
Stage IV Colorectal Cancer 		disease Digestive System Diseases; Neoplasms Neoplastic Process 19 2 0.010 None 1.000 1 2019 2019
CUI: C3146251
Disease: Stage IV Colorectal Cancer AJCC v7
Stage IV Colorectal Cancer AJCC v7 		disease Neoplastic Process 19 2 0.010 None 1.000 1 2019 2019
CUI: C0038441
Disease: Stress Disorders, Traumatic
Stress Disorders, Traumatic 		group Mental Disorders Mental or Behavioral Dysfunction 20 0.010 None 1.000 1 2019 2019
CUI: C0238478
Disease: Transient erythroblastopenia of childhood
Transient erythroblastopenia of childhood 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 23 0.010 None 1.000 1 2019 2019
CUI: C0032708
Disease: Disorders of Porphyrin Metabolism
Disorders of Porphyrin Metabolism 		group Nutritional and Metabolic Diseases Disease or Syndrome 26 7 0.010 None 1.000 1 2005 2005
CUI: C0342200
Disease: Endemic Cretinism
Endemic Cretinism 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Endocrine System Diseases Disease or Syndrome 26 0.200 None 1.000 1 2010 2010
CUI: C0022541
Disease: Kearns-Sayre syndrome
Kearns-Sayre syndrome 		disease Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases; Eye Diseases; Musculoskeletal Diseases; Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 29 5 0.010 None 1.000 1 2016 2016
CUI: C0151785
Disease: Disease of mucous membrane
Disease of mucous membrane 		group Pathological Conditions, Signs and Symptoms Disease or Syndrome 30 0.010 None 1.000 1 2016 2016
CUI: C1096458
Disease: Vascular occlusion
Vascular occlusion 		disease Cardiovascular Diseases Disease or Syndrome 30 2 0.010 None 1.000 1 2013 2013
CUI: C1273070
Disease: Left ventricular diastolic dysfunction
Left ventricular diastolic dysfunction 		disease Cardiovascular Diseases Disease or Syndrome 31 1 0.020 None 1.000 2 1 2008 2019
CUI: C0746731
Disease: Acute myocardial ischemia
Acute myocardial ischemia 		disease Cardiovascular Diseases Disease or Syndrome 32 2 0.010 None 1.000 1 2017 2017