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Gsd Type I
GSD type I
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Inborn errors of metabolism
GSD type III
GSD type V
GSD type II
Galactose-- 1-phosphate uridylyltransferase galactosemia
Glycogen storage disease
Essential fructosuria
Inborn error of metabolism
Hepatology
(8)
GSD type IV
GSD type 0
Glycogen
Hepatomegaly
Cirrhosis
Cirrhosis
GSD type III
GSD type II
Glycogen storage disease
more...
Autosomal recessive disorders
Galactose epimerase deficiency
Glycogen storage disease type vii
GSD type III
GSD type V
GSD type II
Galactose-- 1-phosphate uridylyltransferase galactosemia
Essential fructosuria
Genetic disorders
(9)
Inherited diseases
GSD type III
GSD type IV
GSD type V
GSD type II
GSD type II
Galactose-- 1-phosphate uridylyltransferase galactosemia
Galactose epimerase deficiency
Glycogen storage disease type vii
Essential fructosuria
more...
Genetic disorder
GSD type III
GSD type IV
Galactose-- 1-phosphate uridylyltransferase galactosemia
Galactose epimerase deficiency
Glycogen storage disease type vii
Nutrition disorder
Hers' Disease
GSD type IV
GSD type 0
Essential fructosuria
Nutrition
Galactose metabolism
Fructose
Glycogen
EC 2.4.1
Glycogen debranching enzyme
Myophosphorylase
Branching enzyme
Carbohydrates
Glycolysis
Glucosidase
Glycogen
Diseases and disorders
(14)
Fructose bisphosphatase deficiency
Hematologic disease
Hyperlipidemia
Diabetes mellitus type 1
Low blood sugar
Low blood sugar
Hyperuricemia
GSD type IV
GSD type II
Galactose-- 1-phosphate uridylyltransferase galactosemia
Glycogen storage disease
Glycogen storage disease type vii
Essential fructosuria
Inborn error of metabolism
Cirrhosis
more...
Signs and tests
Biopsy of liver
Blood sugar test
Lactic acid blood test
Triglyceride level
Uric acid blood test
See also
(20)
Enzymes
Glucose 6-phosphatase
Metabolism
Pentose phosphate pathway
PFKM
PFKM
Acid alpha-glucosidase
Type VII
Autosomal recessive
Disaccharide
Acid maltase
Pyruvate carboxylase deficiency
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Myeloid
Emedicine
Genetic counseling
Catabolism
Hepatic
Lysosomal
Ketotic hypoglycemia
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