TCF7L2, transcription factor 7 like 2, 6934

N. diseases: 257; N. variants: 70
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: C0271651
Disease: Impaired glucose tolerance in obese
Impaired glucose tolerance in obese
phenotype Nutritional and Metabolic Diseases Disease or Syndrome 1 0.010 None 1.000 1 2008 2008
CUI: C3896643
Disease: New Onset Diabetes After Transplant
New Onset Diabetes After Transplant
disease Nutritional and Metabolic Diseases; Endocrine System Diseases Disease or Syndrome 6 1 0.010 None 1.000 1 2009 2009
CUI: C0271638
Disease: Type 2 diabetes mellitus in obese
Type 2 diabetes mellitus in obese
disease Nutritional and Metabolic Diseases; Endocrine System Diseases Disease or Syndrome 7 4 0.010 None 1.000 1 1 2008 2008
Ankle brachial pressure index (observable entity)
phenotype Clinical Attribute 7 40 0.100 None 1.000 1 1 2012 2012
CUI: C0155826
Disease: Chronic nasopharyngitis
Chronic nasopharyngitis
disease Infections; Respiratory Tract Diseases; Stomatognathic Diseases; Otorhinolaryngologic Diseases Disease or Syndrome 12 0.010 None 1.000 1 2019 2019
CUI: C0020875
Disease: Ileal Diseases
Ileal Diseases
group Digestive System Diseases Disease or Syndrome 14 7 0.010 None 1.000 1 2007 2007
CUI: C0202098
Disease: Insulin measurement
Insulin measurement
phenotype Laboratory Procedure 15 25 0.100 None 1.000 1 1 2011 2011
CUI: C0017741
Disease: Glucose tolerance test
Glucose tolerance test
phenotype Laboratory Procedure 17 28 0.100 None 1.000 1 1 2010 2010
CUI: C0342546
Disease: Premature adrenarche
Premature adrenarche
disease Disease or Syndrome 18 11 0.010 None < 0.001 1 2 2009 2009
CUI: C0600520
Disease: Left Ventricle Remodeling
Left Ventricle Remodeling
phenotype Pathological Conditions, Signs and Symptoms Organ or Tissue Function 21 0.300 None 1.000 1 2018 2018
CUI: C0600519
Disease: Ventricular Remodeling
Ventricular Remodeling
phenotype Pathological Conditions, Signs and Symptoms Organ or Tissue Function 24 0.300 None 1.000 1 2018 2018
CUI: C1842402
Disease: TROPICAL CALCIFIC PANCREATITIS
TROPICAL CALCIFIC PANCREATITIS
disease Digestive System Diseases; Nutritional and Metabolic Diseases Disease or Syndrome 24 13 0.010 None 1.000 1 2 2008 2008
CUI: C1272321
Disease: Autoantibody measurement
Autoantibody measurement
phenotype Laboratory Procedure 27 52 0.100 None 1.000 1 1 2009 2009
CUI: C4703555
Disease: Decreased waist to hip ratio
Decreased waist to hip ratio
phenotype Finding 28 0.100 None 0
CUI: C0746556
Disease: metabolic disturbance
metabolic disturbance
disease Disease or Syndrome 29 4 0.020 None 1.000 2 1 2015 2018
CUI: C0259749
Disease: Autonomic neuropathy
Autonomic neuropathy
disease Nervous System Diseases Disease or Syndrome 29 7 0.010 None 1.000 1 1 2013 2013
CUI: C0015306
Disease: Hereditary Multiple Exostoses
Hereditary Multiple Exostoses
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Musculoskeletal Diseases Congenital Abnormality 32 51 0.010 None 1.000 1 1 2015 2015
Adenocarcinoma of the gastroesophageal junction
disease Digestive System Diseases; Neoplasms Neoplastic Process 32 6 0.010 None 1.000 1 2 2019 2019
CUI: C0742132
Disease: cervical cancer metastasis
cervical cancer metastasis
disease Neoplastic Process 35 0.010 None 1.000 1 2017 2017
CUI: C4524040
Disease: Atherogenic dyslipidaemia
Atherogenic dyslipidaemia
disease Disease or Syndrome 36 9 0.010 None 1.000 1 1 2009 2009
CUI: C1442903
Disease: Exostoses
Exostoses
phenotype Musculoskeletal Diseases Disease or Syndrome 37 0.010 None 1.000 1 2015 2015
Latent Autoimmune Diabetes in Adults
disease Nutritional and Metabolic Diseases; Immune System Diseases; Endocrine System Diseases Disease or Syndrome 39 12 0.040 None 1.000 4 1 2010 2019
CUI: C2985290
Disease: Fetal Alcohol Spectrum Disorders
Fetal Alcohol Spectrum Disorders
group Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Chemically-Induced Disorders Disease or Syndrome; Congenital Abnormality 46 2 0.010 None 1.000 1 2019 2019
Latent autoimmune diabetes mellitus in adult
disease Nutritional and Metabolic Diseases; Immune System Diseases; Endocrine System Diseases Disease or Syndrome 49 12 0.080 None 1.000 8 1 2008 2019
CUI: C0017979
Disease: Glycosuria
Glycosuria
phenotype Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Finding 53 7 0.100 None 1.000 1 1 2019 2019