GCG, glucagon, 2641

N. diseases: 441; N. variants: 10
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: C0271712
Disease: Hypoglycemia of childhood
Hypoglycemia of childhood 		disease Nutritional and Metabolic Diseases Disease or Syndrome 1 0.020 None 1.000 2 2018 2020
CUI: C0007397
Disease: Catastrophic Illness
Catastrophic Illness 		disease Pathological Conditions, Signs and Symptoms Disease or Syndrome 1 0.010 None 1.000 1 2017 2017
CUI: C0341274
Disease: Acute radiation enteritis
Acute radiation enteritis 		disease Digestive System Diseases; Wounds and Injuries Disease or Syndrome 1 0.010 None 1.000 1 2019 2019
CUI: C1881406
Disease: Lipase Hypersecretion Syndrome
Lipase Hypersecretion Syndrome 		phenotype Pathological Conditions, Signs and Symptoms Disease or Syndrome 1 0.010 None 1.000 1 2019 2019
CUI: C4476847
Disease: Short bowel
Short bowel 		disease Congenital Abnormality 1 0.010 None 1.000 1 2017 2017
CUI: C0221243
Disease: Necrolytic Migratory Erythema
Necrolytic Migratory Erythema 		disease Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases Disease or Syndrome 2 0.020 None 1.000 2 2017 2018
CUI: C0151911
Disease: Generalized Spasms
Generalized Spasms 		phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases Finding 2 0.300 None 1.000 1 1980 1980
CUI: C0235229
Disease: Ciliary Body Spasm
Ciliary Body Spasm 		phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases Finding 2 0.300 None 1.000 1 1980 1980
CUI: C0239233
Disease: Early satiety
Early satiety 		phenotype Mental Disorders Sign or Symptom 2 0.010 None 1.000 1 2017 2017
CUI: C4476813
Disease: Class I obesity
Class I obesity 		phenotype Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases Disease or Syndrome 2 3 0.010 None 1.000 1 2017 2017
CUI: C0271719
Disease: Glucagon resistance
Glucagon resistance 		disease Disease or Syndrome 3 0.020 None 1.000 2 2018 2019
CUI: C0271706
Disease: Hyperplasia of pancreatic islet beta cell
Hyperplasia of pancreatic islet beta cell 		disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases Disease or Syndrome 3 0.010 None 1.000 1 2017 2017
CUI: C0342311
Disease: Neuroglycopenia
Neuroglycopenia 		disease Nutritional and Metabolic Diseases Disease or Syndrome 3 0.010 None 1.000 1 2019 2019
CUI: C4274352
Disease: Chronic intestinal failure
Chronic intestinal failure 		disease Disease or Syndrome 3 0.010 None 1.000 1 2018 2018
CUI: C1834014
Disease: Oculopharyngodistal Myopathy
Oculopharyngodistal Myopathy 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases Disease or Syndrome 4 0.020 None 1.000 2 2001 2004
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: C0235430
Disease: Ketonemia
Ketonemia 		phenotype Nutritional and Metabolic Diseases Disease or Syndrome 4 0.010 None 1.000 1 2017 2017
CUI: C1740821
Disease: Slowly progressive insulin dependent diabetes
Slowly progressive insulin dependent diabetes 		disease Disease or Syndrome 4 0.010 None 1.000 1 2019 2019
CUI: C3495840
Disease: Pancreatic steatosis
Pancreatic steatosis 		disease Disease or Syndrome 4 0.010 None 1.000 1 2017 2017
CUI: C0271885
Disease: Hypothalamic obesity
Hypothalamic obesity 		disease Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases Disease or Syndrome 5 0.010 None 1.000 1 2020 2020
CUI: C0860634
Disease: Psychogenic coma
Psychogenic coma 		phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases Mental or Behavioral Dysfunction 5 0.300 None 1.000 1 1999 1999
CUI: C0877173
Disease: Food aversion
Food aversion 		disease Mental or Behavioral Dysfunction 5 0.010 None 1.000 1 2018 2018
CUI: C1257861
Disease: Colonic Inertia
Colonic Inertia 		phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 6 0.300 None 1.000 1 2002 2002
CUI: C4324584
Disease: Periprocedural myocardial infarction
Periprocedural myocardial infarction 		disease Disease or Syndrome 6 1 0.010 None 1.000 1 2019 2019
CUI: C0237326
Disease: Dyschezia
Dyschezia 		phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 7 0.300 None 1.000 1 2002 2002