GLP1R, glucagon like peptide 1 receptor, 2740

N. diseases: 288; N. variants: 7
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: C0016807
Disease: Functional disorder of intestine
Functional disorder of intestine 		disease Digestive System Diseases Disease or Syndrome 4 0.010 None 1.000 1 2019 2019
CUI: C4021982
Disease: Abnormal eating behavior
Abnormal eating behavior 		phenotype Mental or Behavioral Dysfunction 8 0.010 None 1.000 1 2018 2018
CUI: C2004461
Disease: Bowel dysfunction
Bowel dysfunction 		disease Digestive System Diseases Disease or Syndrome 16 1 0.010 None 1.000 1 2019 2019
CUI: C4054325
Disease: Obesity Related Glomerulopathy
Obesity Related Glomerulopathy 		disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 16 0.010 None 1.000 1 2018 2018
CUI: C0948908
Disease: Nephrotoxic serum nephritis
Nephrotoxic serum nephritis 		disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 17 1 0.010 None 1.000 1 2020 2020
CUI: C0036992
Disease: Short Bowel Syndrome
Short Bowel Syndrome 		disease Pathological Conditions, Signs and Symptoms; Digestive System Diseases Disease or Syndrome 21 1 0.020 None 1.000 2 2017 2019
CUI: C1704374
Disease: Carcinoma of Endocrine Gland
Carcinoma of Endocrine Gland 		disease Neoplasms; Endocrine System Diseases Neoplastic Process 22 0.010 None 1.000 1 2019 2019
CUI: C0271710
Disease: Reactive hypoglycemia
Reactive hypoglycemia 		disease Nutritional and Metabolic Diseases Disease or Syndrome 23 0.020 None 1.000 2 2017 2019
CUI: C0017689
Disease: Glucagonoma
Glucagonoma 		disease Digestive System Diseases; Neoplasms; Endocrine System Diseases Neoplastic Process 23 1 0.010 None 1.000 1 1985 1985
CUI: C0043207
Disease: Wolfram Syndrome
Wolfram Syndrome 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Eye Diseases; Male Urogenital Diseases; Nervous System Diseases; Endocrine System Diseases; Otorhinolaryngologic Diseases Disease or Syndrome 28 7 0.020 None 1.000 2 2018 2019
CUI: C3160761
Disease: Diabetic dyslipidaemia
Diabetic dyslipidaemia 		disease Disease or Syndrome 28 11 0.010 None 1.000 1 2018 2018
CUI: C1442837
Disease: Myocardial necrosis
Myocardial necrosis 		disease Cardiovascular Diseases Disease or Syndrome 30 2 0.010 None 1.000 1 2018 2018
CUI: C0342190
Disease: C-cell hyperplasia of thyroid
C-cell hyperplasia of thyroid 		disease Pathological Conditions, Signs and Symptoms; Endocrine System Diseases Disease or Syndrome 35 16 0.030 None 1.000 3 2010 2017
CUI: C4728082
Disease: Severe hypoglycaemia
Severe hypoglycaemia 		disease Disease or Syndrome 36 2 0.020 None 1.000 2 2017 2018
CUI: C0271708
Disease: Fasting Hypoglycemia
Fasting Hypoglycemia 		phenotype Nutritional and Metabolic Diseases Disease or Syndrome 39 1 0.010 None 1.000 1 2012 2012
CUI: C0858600
Disease: Taste sweet
Taste sweet 		phenotype Sign or Symptom 41 3 0.010 None 1.000 1 2017 2017
CUI: C0016977
Disease: Gall Bladder Diseases
Gall Bladder Diseases 		group Digestive System Diseases Disease or Syndrome 42 4 0.010 None 1.000 1 2017 2017
CUI: C1854520
Disease: SEBASTIAN SYNDROME
SEBASTIAN SYNDROME 		disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Otorhinolaryngologic Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 42 13 0.010 None 1.000 1 2017 2017
CUI: C4721209
Disease: Metastatic human epidermal growth factor 2 positive carcinoma of breast
Metastatic human epidermal growth factor 2 positive carcinoma of breast 		disease Neoplasms; Skin and Connective Tissue Diseases Neoplastic Process 42 0.010 None 1.000 1 2018 2018
CUI: C1857941
Disease: Brooke-Spiegler syndrome
Brooke-Spiegler syndrome 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Skin and Connective Tissue Diseases Disease or Syndrome 45 8 0.010 None 1.000 1 2017 2017
CUI: C3845502
Disease: Myocardial infarction, stroke
Myocardial infarction, stroke 		disease Disease or Syndrome 46 3 0.010 None 1.000 1 2018 2018
CUI: C2960127
Disease: Heart failure with normal ejection fraction
Heart failure with normal ejection fraction 		disease Cardiovascular Diseases Disease or Syndrome 47 0.010 None 1.000 1 2018 2018
CUI: C1864903
Disease: Hyperinsulinemic hypoglycemia
Hyperinsulinemic hypoglycemia 		disease Nutritional and Metabolic Diseases Disease or Syndrome 52 6 0.040 None 1.000 4 2017 2019
CUI: C0008325
Disease: Cholecystitis
Cholecystitis 		disease Digestive System Diseases Disease or Syndrome 55 3 0.010 None 1.000 1 2019 2019
CUI: C3665365
Disease: Arteriosclerotic cardiovascular disease, NOS
Arteriosclerotic cardiovascular disease, NOS 		disease Cardiovascular Diseases Disease or Syndrome 58 5 0.010 None 1.000 1 2019 2019