GSTT1, glutathione S-transferase theta 1, 2952

N. diseases: 541; N. variants: 0
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: C0744855
Disease: hepatitis immune
hepatitis immune 		disease Disease or Syndrome 4 0.040 None 1.000 4 2001 2018
CUI: C4733575
Disease: newly diagnosed non-small cell lung cancer
newly diagnosed non-small cell lung cancer 		disease Neoplastic Process 4 3 0.010 None 1.000 1 2004 2004
CUI: C1883486
Disease: Uterine Corpus Cancer
Uterine Corpus Cancer 		disease Neoplastic Process 5 0.010 None 1.000 1 2011 2011
CUI: C0338507
Disease: Non-arteritic ischemic optic neuropathy
Non-arteritic ischemic optic neuropathy 		disease Eye Diseases; Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 6 3 0.010 None 1.000 1 2009 2009
CUI: C0860168
Disease: Distal colitis
Distal colitis 		disease Digestive System Diseases Disease or Syndrome 6 3 0.010 None 1.000 1 2011 2011
CUI: C0920506
Disease: Environment-Related Malignant Neoplasm
Environment-Related Malignant Neoplasm 		disease Neoplasms Neoplastic Process 6 2 0.010 None 1.000 1 1998 1998
CUI: C0034734
Disease: Raynaud Disease
Raynaud Disease 		disease Cardiovascular Diseases Disease or Syndrome 7 0.300 None 1.000 1 2006 2006
CUI: C4068743
Disease: Juvenile open angle
Juvenile open angle 		disease Disease or Syndrome 7 1 0.010 None 1.000 1 2017 2017
CUI: C0027663
Disease: Neoplasms, Multiple Primary
Neoplasms, Multiple Primary 		phenotype Neoplasms Neoplastic Process 8 0.010 None 1.000 1 2004 2004
CUI: C1518005
Disease: Low Grade Cervical Squamous Intraepithelial Neoplasia
Low Grade Cervical Squamous Intraepithelial Neoplasia 		disease Pathological Conditions, Signs and Symptoms; Neoplasms; Female Urogenital Diseases and Pregnancy Complications Neoplastic Process 8 0.010 None 1.000 1 1994 1994
CUI: C2880562
Disease: Age-related cortical cataract
Age-related cortical cataract 		disease Acquired Abnormality 9 2 0.010 None 1.000 1 2012 2012
CUI: C3826743
Disease: Anemia in children
Anemia in children 		disease Disease or Syndrome 9 0.010 None 1.000 1 2004 2004
CUI: C0340170
Disease: Complicated pneumoconiosis
Complicated pneumoconiosis 		disease Respiratory Tract Diseases; Occupational Diseases Disease or Syndrome 13 0.010 None 1.000 1 2005 2005
CUI: C0858681
Disease: Vitiligo vulgaris
Vitiligo vulgaris 		disease Skin and Connective Tissue Diseases Disease or Syndrome 13 5 0.010 None 1.000 1 2013 2013
CUI: C1859972
Disease: ADRENOCORTICAL CARCINOMA, HEREDITARY
ADRENOCORTICAL CARCINOMA, HEREDITARY 		disease Neoplasms; Endocrine System Diseases Neoplastic Process 13 7 0.010 None 1.000 1 2015 2015
CUI: C2930617
Disease: Pulmonary Fibrosis - from Asbestos Exposure
Pulmonary Fibrosis - from Asbestos Exposure 		disease Respiratory Tract Diseases; Occupational Diseases Disease or Syndrome 14 0.300 None 1.000 1 2007 2007
CUI: C4324396
Disease: Immune-mediated hepatitis
Immune-mediated hepatitis 		disease Disease or Syndrome 15 0.010 None 1.000 1 2013 2013
CUI: C0004403
Disease: Autosome Abnormalities
Autosome Abnormalities 		group Pathological Conditions, Signs and Symptoms Cell or Molecular Dysfunction 16 0.300 None 1.000 3 2006 2013
CUI: C0008625
Disease: Chromosome Aberrations
Chromosome Aberrations 		group Pathological Conditions, Signs and Symptoms Cell or Molecular Dysfunction 16 0.300 None 1.000 3 2006 2013
CUI: C0004093
Disease: Asthenia
Asthenia 		phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 16 3 0.010 None 1.000 1 2013 2013
CUI: C0334619
Disease: HODGKIN'S AND NON-HODGKIN'S LYMPHOMA
HODGKIN'S AND NON-HODGKIN'S LYMPHOMA 		disease Neoplastic Process 17 1 0.020 None 1.000 2 2007 2013
CUI: C0009373
Disease: Colonic Diseases
Colonic Diseases 		group Digestive System Diseases Disease or Syndrome 17 8 0.010 None 1.000 1 2001 2001
CUI: C0042485
Disease: Venous Insufficiency
Venous Insufficiency 		disease Cardiovascular Diseases Disease or Syndrome 17 1 0.010 None 1.000 1 2013 2013
CUI: C1827377
Disease: Slow acetylator due to N-acetyltransferase enzyme variant
Slow acetylator due to N-acetyltransferase enzyme variant 		disease Disease or Syndrome 20 8 0.040 None 1.000 4 2000 2006
CUI: C0031736
Disease: Polymorphous light eruption
Polymorphous light eruption 		disease Skin and Connective Tissue Diseases; Immune System Diseases Disease or Syndrome 20 0.010 None 1.000 1 2013 2013