GCK, glucokinase, 2645

N. diseases: 210; N. variants: 182
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.
Hyperinsulinemic hypoglycemia, familial, 3
disease Nutritional and Metabolic Diseases Disease or Syndrome 1 11 0.700 strong 1.000 9 11 1998 2017
CUI: C2609269
Disease: Fasting hyperglycaemia
Fasting hyperglycaemia
phenotype Finding 1 0.300 strong 0
DIABETES MELLITUS, NONINSULIN-DEPENDENT, LATE-ONSET
disease Finding 1 1 0.100 None 0 1
CUI: C0271702
Disease: Iatrogenic hyperinsulinism
Iatrogenic hyperinsulinism
phenotype Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases Disease or Syndrome 2 0.010 None 1.000 1 2019 2019
Hyperinsulinemic hypoglycemia, familial, 1
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases Disease or Syndrome 3 147 0.300 None 1.000 1 2004 2004
Hyperinsulinemic hypoglycemia, familial, 2
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases Disease or Syndrome 3 50 0.300 None 1.000 1 2004 2004
Abnormality of the autonomic nervous system
phenotype Anatomical Abnormality 3 0.100 None 0
CUI: C0342317
Disease: Loss of hypoglycemic warning
Loss of hypoglycemic warning
disease Disease or Syndrome 4 1 0.010 None 1.000 1 2008 2008
CUI: C3825462
Disease: Diabetes in youth
Diabetes in youth
disease Disease or Syndrome 4 2 0.010 None 1.000 1 2013 2013
CUI: C0149670
Disease: Disorder of carbohydrate metabolism
Disorder of carbohydrate metabolism
group Nutritional and Metabolic Diseases Disease or Syndrome 5 0.010 None 1.000 1 1992 1992
Transient hypothyroxinaemia of prematurity
disease Disease or Syndrome 6 0.010 None 1.000 1 2017 2017
CUI: C1969875
Disease: Beta-cell dysfunction
Beta-cell dysfunction
phenotype Finding 6 0.100 None 0
CUI: C4330695
Disease: Mitochondrial Diabetes
Mitochondrial Diabetes
disease Nutritional and Metabolic Diseases; Endocrine System Diseases Disease or Syndrome 7 0.010 None 1.000 1 1996 1996
CUI: C1856904
Disease: Reduced pancreatic beta cells
Reduced pancreatic beta cells
phenotype Finding 7 0.100 None 0
Diabetes mellitus autosomal dominant type II (disorder)
disease Nutritional and Metabolic Diseases; Endocrine System Diseases Disease or Syndrome 8 139 1.000 strong 1.000 82 137 1992 2019
CUI: C4020778
Disease: maternal hyperglycemia
maternal hyperglycemia
disease Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases Disease or Syndrome 8 0.020 None 1.000 2 2012 2018
CUI: C4321446
Disease: K ATP Permanent Neonatal Diabetes
K ATP Permanent Neonatal Diabetes
disease Disease or Syndrome 8 2 0.020 None 1.000 2 1 2014 2015
CUI: C0745153
Disease: Hypoglycaemic episode
Hypoglycaemic episode
disease Disease or Syndrome 8 2 0.010 None 1.000 1 1 2009 2009
CUI: C0017926
Disease: Glycogen Storage Disease Type VII
Glycogen Storage Disease Type VII
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases; Nervous System Diseases Disease or Syndrome 9 9 0.010 None 1.000 1 2000 2000
CUI: C1864954
Disease: Fasting hyperinsulinemia
Fasting hyperinsulinemia
phenotype Nutritional and Metabolic Diseases Finding 10 0.100 None 0
CUI: C1969879
Disease: Limb joint contracture
Limb joint contracture
phenotype Finding 10 1 0.100 None 0
Neonatal insulin-dependent diabetes mellitus
phenotype Finding 10 6 0.100 None 0
MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 3 (disorder)
disease Nutritional and Metabolic Diseases; Endocrine System Diseases Disease or Syndrome 12 48 0.060 None 1.000 6 1997 2014
CUI: C0300948
Disease: Caudal Regression Syndrome
Caudal Regression Syndrome
disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases Congenital Abnormality 12 1 0.010 None 1.000 1 2019 2019
CUI: C0027773
Disease: Nesidioblastosis
Nesidioblastosis
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases Disease or Syndrome 12 0.200 None 0