MGMT, O-6-methylguanine-DNA methyltransferase, 4255

N. diseases: 293; N. variants: 14
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: C0032584
Disease: polyps
polyps
phenotype Pathological Conditions, Signs and Symptoms Anatomical Abnormality 284 19 0.100 1.000 10 2001 2014
CUI: C0009376
Disease: Colonic Polyps
Colonic Polyps
phenotype Pathological Conditions, Signs and Symptoms Anatomical Abnormality 46 2 0.010 1.000 1 2011 2011
CUI: C4021976
Disease: Abnormality of the lymphatic system
Abnormality of the lymphatic system
phenotype Anatomical Abnormality 15 0.100 0
CUI: C3546688
Disease: response to temozolomide
response to temozolomide
phenotype Cell Function 1 1 0.100 1 1 2013 2013
CUI: C0041107
Disease: Trisomy
Trisomy
group Pathological Conditions, Signs and Symptoms Cell or Molecular Dysfunction 208 1 0.010 1.000 1 2011 2011
CUI: C0078918
Disease: Albinism, Oculocutaneous
Albinism, Oculocutaneous
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases Congenital Abnormality 32 28 0.010 1.000 1 1 2018 2018
CUI: C0175754
Disease: Agenesis of corpus callosum
Agenesis of corpus callosum
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Pathological Conditions, Signs and Symptoms Congenital Abnormality 316 19 0.010 1.000 1 2005 2005
CUI: C0282160
Disease: Aplasia Cutis Congenita
Aplasia Cutis Congenita
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases Congenital Abnormality 198 7 0.010 1.000 1 2005 2005
Rash and Dermatitis Adverse Event Associated with Chemoradiation
disease Disease or Syndrome 99 27 0.050 1.000 5 2004 2016
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis
disease Digestive System Diseases Disease or Syndrome 914 696 0.030 1.000 3 2003 2011
CUI: C0024814
Disease: Marinesco-Sjogren syndrome
Marinesco-Sjogren syndrome
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Disease or Syndrome 77 12 0.030 0.667 3 2002 2007
CUI: C0023890
Disease: Liver Cirrhosis
Liver Cirrhosis
disease Digestive System Diseases Disease or Syndrome 682 71 0.020 1.000 2 1997 1997
CUI: C0033036
Disease: Atrial Premature Complexes
Atrial Premature Complexes
disease Cardiovascular Diseases; Pathological Conditions, Signs and Symptoms Disease or Syndrome 105 9 0.020 0.500 2 2008 2009
CUI: C0265325
Disease: Turcot syndrome (disorder)
Turcot syndrome (disorder)
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Neoplasms; Nervous System Diseases Disease or Syndrome 49 40 0.020 1.000 2 2008 2015
Infection caused by Helicobacter pylori
disease Disease or Syndrome 307 53 0.020 1.000 2 2009 2010
CUI: C0001857
Disease: AIDS related complex
AIDS related complex
disease Immune System Diseases; Virus Diseases Disease or Syndrome 40 10 0.010 1.000 1 2015 2015
CUI: C0004763
Disease: Barrett Esophagus
Barrett Esophagus
disease Digestive System Diseases; Neoplasms Disease or Syndrome 322 40 0.010 1.000 1 2009 2009
CUI: C0009319
Disease: Colitis
Colitis
disease Digestive System Diseases Disease or Syndrome 607 6 0.010 1.000 1 2008 2008
CUI: C0009447
Disease: Common Variable Immunodeficiency
Common Variable Immunodeficiency
disease Immune System Diseases Disease or Syndrome 151 50 0.010 1.000 1 2003 2003
CUI: C0011615
Disease: Dermatitis, Atopic
Dermatitis, Atopic
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Immune System Diseases; Skin and Connective Tissue Diseases Disease or Syndrome 483 173 0.100 1 1 2015 2015
CUI: C0015625
Disease: Fanconi Anemia
Fanconi Anemia
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases; Nutritional and Metabolic Diseases Disease or Syndrome 289 91 0.010 1.000 1 2009 2009
CUI: C0017168
Disease: Gastroesophageal reflux disease
Gastroesophageal reflux disease
disease Digestive System Diseases Disease or Syndrome 245 13 0.010 1.000 1 1 2008 2008
CUI: C0018133
Disease: Graft-vs-Host Disease
Graft-vs-Host Disease
disease Immune System Diseases Disease or Syndrome 225 8 0.010 1.000 1 2013 2013
CUI: C0019158
Disease: Hepatitis
Hepatitis
disease Digestive System Diseases Disease or Syndrome 316 7 0.010 1 2003 2003
CUI: C0019159
Disease: Hepatitis A
Hepatitis A
disease Digestive System Diseases; Virus Diseases Disease or Syndrome 260 8 0.010 1.000 1 2003 2003