TAS2R38, taste 2 receptor member 38, 5726

N. diseases: 149; N. variants: 5
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: C0920350
Disease: Autoimmune thyroiditis
Autoimmune thyroiditis
disease Immune System Diseases; Endocrine System Diseases Disease or Syndrome 161 76 0.010 None 1.000 1 2005 2005
CUI: C0949541
Disease: Hurthle Cell Tumor
Hurthle Cell Tumor
disease Neoplasms Neoplastic Process 170 9 0.010 None 1.000 1 2017 2017
Poorly Differentiated Thyroid Carcinoma
disease Neoplasms; Endocrine System Diseases Neoplastic Process 54 2 0.010 None 1.000 1 2019 2019
CUI: C1269955
Disease: Tumor Cell Invasion
Tumor Cell Invasion
phenotype Neoplastic Process 6626 169 0.010 None 1.000 1 2019 2019
CUI: C1302401
Disease: Adenoma of large intestine
Adenoma of large intestine
disease Digestive System Diseases; Neoplasms Neoplastic Process 452 213 0.010 None 1.000 1 3 2013 2013
CUI: C1306460
Disease: Primary malignant neoplasm of lung
Primary malignant neoplasm of lung
disease Neoplasms; Respiratory Tract Diseases Neoplastic Process 3894 981 0.010 None 1.000 1 2014 2014
CUI: C1336750
Disease: Thyroid Gland Oncocytic Adenoma
Thyroid Gland Oncocytic Adenoma
disease Neoplasms; Endocrine System Diseases Neoplastic Process 11 0.010 None 1.000 1 2017 2017
familial non-medullary thyroid cancer
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms Neoplastic Process 17 1 0.010 None 1.000 1 2011 2011
CUI: C0025202
Disease: melanoma
melanoma
disease Neoplasms Neoplastic Process 3087 515 0.010 None 1.000 1 2014 2014
CUI: C0030472
Disease: Paraneoplastic Syndromes
Paraneoplastic Syndromes
group Neoplasms Neoplastic Process 28 0.010 None 1.000 1 2018 2018
CUI: C0010674
Disease: Cystic Fibrosis
Cystic Fibrosis
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Respiratory Tract Diseases Disease or Syndrome 852 704 0.010 None 1.000 1 2016 2016
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
disease Cardiovascular Diseases Disease or Syndrome 1576 1178 0.010 None 1.000 1 2005 2005
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
disease Nervous System Diseases Disease or Syndrome 2078 990 0.010 None 1.000 1 2018 2018
CUI: C0850572
Disease: Adenomatous polyp of colon
Adenomatous polyp of colon
disease Pathological Conditions, Signs and Symptoms Neoplastic Process 7 3 0.010 None 1.000 1 3 2011 2011
CUI: C0032584
Disease: polyps
polyps
phenotype Pathological Conditions, Signs and Symptoms Anatomical Abnormality 390 18 0.010 None 1.000 1 2018 2018
CUI: C0035204
Disease: Respiration Disorders
Respiration Disorders
group Respiratory Tract Diseases Disease or Syndrome 208 6 0.010 None 1.000 1 2016 2016
CUI: C0035242
Disease: Respiratory Tract Diseases
Respiratory Tract Diseases
group Respiratory Tract Diseases Disease or Syndrome 198 109 0.010 None 1.000 1 2016 2016
CUI: C0011389
Disease: Dental Plaque
Dental Plaque
phenotype Stomatognathic Diseases Disease or Syndrome 27 0.010 None 1.000 1 2016 2016
CUI: C0014544
Disease: Epilepsy
Epilepsy
disease Nervous System Diseases Disease or Syndrome 1215 339 0.010 None 1.000 1 2005 2005
CUI: C0025149
Disease: Medulloblastoma
Medulloblastoma
disease Neoplasms Neoplastic Process 862 115 0.010 None 1.000 1 2000 2000
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach
disease Digestive System Diseases; Neoplasms Neoplastic Process 3806 615 0.010 None 1.000 1 2016 2016
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
group Cardiovascular Diseases Disease or Syndrome 2322 1085 0.010 None 1.000 1 2008 2008
CUI: C0020175
Disease: Hunger
Hunger
phenotype Behavior and Behavior Mechanisms Sign or Symptom 70 12 0.010 None 1.000 1 2010 2010
CUI: C0018213
Disease: Graves Disease
Graves Disease
disease Eye Diseases; Immune System Diseases; Endocrine System Diseases Disease or Syndrome 585 352 0.010 None 1.000 1 2003 2003
CUI: C0013264
Disease: Muscular Dystrophy, Duchenne
Muscular Dystrophy, Duchenne
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases Disease or Syndrome 375 170 0.010 None 1.000 1 2017 2017