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5C51.3 Glycogen storage disease

International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01

The term Glycogen storage disease characterises a group of heterogeneous diseases resulting from defects in the process of glycogen synthesis or breakdown within muscles, liver, and other cell types.

inclusions

• Glycogen storage disease due to LAMP-2 deficiency
• Glycogen storage disease due to glycogen debranching enzyme deficiency
• Glycogen storage disease due to muscle glycogen phosphorylase deficiency
• Glycogen storage disease due to liver glycogen phosphorylase deficiency
• Glycogen storage disease due to GLUT2 deficiency
• Glycogen storage disease due to aldolase A deficiency
• Glycogen storage disease due to muscle beta-enolase deficiency
• Glycogen storage disease due to phosphoglucomutase deficiency
• Glycogen storage disease due to glycogenin deficiency
• Glycogen storage disease due to phosphoglycerate kinase 1 deficiency
• Glycogen storage disease due to lactate dehydrogenase deficiency
• Glycogen storage disease due to muscle pyruvate kinase deficiency
• Dilated cardiomyopathy due to glycogen branching enzyme deficiency

synonyms

• Glycogen storage disease
• Glycogenosis
• GSD - [Glycogen storage disease]
• glycogen thesaurismosis
• diffuse glycogenosis
• generalised glycogen storage disease
• generalised glycogenosis
• generalised glycogen storage disease of infants
• glycogen synthase deficiency
• Glycogen storage disease due to glycogen synthase deficiency
• Glycogen storage disease type 0
• Glycogenosis type 0
• GSD type 0
• deficiency of glycogen synthetase
• Glycogen storage disease due to liver glycogen synthase deficiency
• GSD type 0A
• Glycogen storage disease type 0A
• Glycogenosis type 0A
• Glycogen storage disease due to muscle or heart glycogen synthase deficiency
• Glycogen storage disease type 0B
• Glycogenosis type 0B
• GSD type 0B
• Cardiomyopathy-exercise intolerance due to muscle and heart glycogen deficiency
• Glycogen storage disease due to glucose-6-phosphate system deficiency
• Glycogen storage disease type 1
• Glycogenosis type 1
• GSD type 1
• Hepatorenal glycogenosis
• Von Gierke disease
• HERS - [hepatorenal glycogen storage disease]
• glycogen storage disease of liver and kidney
• hepatorenal glycogen storage disease
• Glycogen storage disease due to glucose-6-phosphatase deficiency
• Glycogen storage disease type 1A
• Glycogenosis type 1A
• GSD type 1A
• g6pd - [glucose-6-phosphate dehydrogenase deficiency]
• glucose-6-phosphatase deficiency
• deficiency of g-6pd
• Glycogen storage disease due to glucose-6-phosphate transport defect
• Glycogen storage disease type 1B
• Glycogenosis type 1B
• GSD1B
• Glycogen storage disease type non-1A
• Glycogenosis type non-1A
• Glycogen storage disease due to glucose-6-phosphate translocase deficiency
• Glucose-6-phosphate dehydrogenase deficiency
• Glycogen storage disease due to acid maltase deficiency
• Glycogen storage disease type 2
• Glycogenosis type 2
• GSD type 2
• Acid maltase deficiency
• Pompe disease
• Acid alpha-1,4-glucosidase deficiency
• alpha-glucosidase deficiency
• deficiency of amyloglucosidase
• Glycogen storage disease due to acid maltase deficiency, infantile onset
• Glycogen storage disease type 2, infantile onset
• Glycogenosis type 2, infantile onset
• GSD2, infantile onset
• Glycogen storage disease due to acid alpha-1,4-glucosidase deficiency, infantile onset
• Infantile Pompe disease
• lysosomal alpha-1,4-glucosidase deficiency (disorder)
• Glycogen storage disease due to acid maltase deficiency, juvenile onset
• Glycogen storage disease due to acid maltase deficiency, adult onset
• Deficiency of exo-1,4-alpha-glucosidase
• Deficiency of glucan 1,4-alpha-glucosidase
• Deficiency of gamma-amylase
• Deficiency of glucoamylase
• Deficiency of glucoinvertase
• Deficiency of glucosidosucrase
• Deficiency of maltase
• Glycogen storage disease due to LAMP-2 deficiency
• Glycogen storage disease type 2B
• Glycogenosis type 2B
• GSD type 2B
• Lysosomal glycogen storage disease with normal acid maltase activity
• Danon disease
• Glycogen storage disease due to glycogen debranching enzyme deficiency
• Glycogen storage disease type 3
• Glycogenosis type 3
• GSD type 3
• Amylo-1,6-glucosidase deficiency
• Glycogen debranching deficiency
• Cori-Forbes disease
• Cori disease
• Forbes disease
• Forbes glycogen storage disease
• debrancher deficiency glycogen storage disease
• debrancher enzyme deficiency
• deficiency of 6-alpha-d-glucosidase
• amylo-1,6-glucosidase deficiency disorder
• Glycogen storage disease due to muscle glycogen phosphorylase deficiency
• Glycogen storage disease type 5
• Glycogenosis type 5
• GSD type 5
• Myophosphorylase deficiency
• McArdle disease
• myophosphorylase deficiency glycogenosis
• Glycogen storage disease due to liver glycogen phosphorylase deficiency
• Glycogenosis due to liver phosphorylase deficiency
• Glycogen storage disease type 6
• Glycogenosis type 6
• GSD type 6
• Glycogen storage disease type 6B
• Glycogenosis type 6B
• GSD type 6B
• Hers disease
• deficiency of hepatophosphorylase
• Glycogen storage disease due to muscle phosphofructokinase deficiency
• Glycogen storage disease type 7
• Glycogenosis type 7
• GSD type 7
• Muscle phosphofructokinase deficiency
• Tarui disease
• anaemia due to phosphofructo-aldolase deficiency
• Glycogen storage disease due to glycogen phosphorylase kinase deficiency
• Glycogenosis due to phosphorylase kinase deficiency
• GSD due to phosphorylase kinase deficiency
• Glycogen storage disease due to liver glycogen phosphorylase kinase deficiency
• Hepatic phosphorylase kinase deficiency
• Glycogen storage disease type 8
• Glycogenosis type 8
• GSD8 - [glycogen storage disease type 8]
• Glycogen storage disease type 6A
• Glycogen storage disease type 9A
• Glycogen storage disease type 9C
• Glycogenosis type 6A
• Glycogenosis type 9A
• Glycogenosis type 9C
• GSD type 9C - [glycogen storage disease type 9C]
• GSD6A - [glycogen storage disease type 6A]
• GSD9A - [glycogen storage disease type 9A]
• Glycogen storage disease due to liver or muscle glycogen phosphorylase kinase deficiency
• Glycogen storage disease type 9B
• Glycogenosis type 9B
• GSD type 9B
• Glycogen storage disease type 9
• Glycogenosis type 9
• GSD9 - [glycogen storage disease type 9]
• Glycogen storage disease due to heart glycogen phosphorylase kinase deficiency
• Glycogen storage disease of heart
• Cardiac glycogenosis
• Glycogen storage disease type 9F
• Glycogenosis type 9F
• GSD9F
• glycogen heart disease
• glycogenic myocardial infiltration
• glycogenic myocardium infiltration
• cardiomegalia glycogenica diffusa
• Glycogen storage disease due to muscle glycogen phosphorylase kinase deficiency
• GSD9D - [glycogen storage disease type IXD]
• Glycogen storage disease type 9D
• Glycogen storage disease type 9E
• Glycogenosis type 9D
• Glycogenosis type 9E
• GSD9E
• muscle glycogen phosphorylase deficiency
• glycogenosis type IXE
• Glycogen storage disease due to muscle phosphoglycerate mutase deficiency
• Glycogen storage disease type 10
• Glycogenosis type 10
• GSD type 10
• Di Mauro disease
• Glycogen storage disease due to GLUT2 deficiency
• Glycogen storage disease type 11
• Glycogenosis type 11
• GSD type 11
• Fanconi-Bickel glycogenosis
• Bickel-Fanconi disease
• Facilitated glucose transporter protein type 2 deficiency
• Fanconi-Bickel syndrome
• Glycogen storage disease due to aldolase A deficiency
• Glycogen storage disease type 12
• Glycogenosis type 12
• GSD type 12
• Glycogen storage disease due to muscle beta-enolase deficiency
• Glycogen storage disease type 13
• Glycogenosis type 13
• GSD type 13
• Glycogen storage disease due to phosphoglucomutase deficiency
• Glycogen storage disease type 14
• Glycogenosis type 14
• GSD type 14
• Glycogen storage disease due to glycogenin deficiency
• Glycogen storage disease type 15
• GSD type 15
• Glocogenosis type 15
• Glycogen storage disease due to phosphoglycerate kinase 1 deficiency
• Glycogenosis due to phosphoglycerate kinase 1 deficiency
• GSD due to phosphoglycerate kinase 1 deficiency
• Glycogen storage disease due to lactate dehydrogenase deficiency
• Glycogenosis due to lactate dehydrogenase deficiency
• GSD due to lactate dehydrogenase deficiency
• Glycogen storage disease due to muscle pyruvate kinase deficiency
• Glycogenosis due to muscle pyruvate kinase deficiency
• GSD due to muscle pyruvate kinase deficiency
• Glycogen storage liver disease
• hepatomegalia glycogenica diffusa
• liver glycogen disease
• liver phosphorylase deficiency
• Glycogen storage disease due to branching-transferase deficiency
• Andersen disease
• brancher deficiency glycogen storage disease
• branching enzyme deficiency
• branching-transferase deficiency glycogenosis
• deficiency of 1,4-alpha-glucan branching enzyme
• deficiency of amylo-(1,4,6)-transglycosylase
• Glycogen storage disease type 4
• Glycogenosis type 4
• GSD- [Glycogen storage disease] type 4
• Dilated cardiomyopathy due to glycogen branching enzyme deficiency
• Amylopectinosis
• dilated cardiomyopathy due to Andersen's disease
• dilated cardiomyopathy due to glycogen storage disease type 4 (GSD4)

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