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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