ONKI3 | Medical Subject Headings

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Glycogen Storage Disease Type III

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Hierarchy:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Metabolism, Inborn Errors ∟ Carbohydrate Metabolism, Inborn Errors ∟ Glycogen Storage Disease ∟ Glycogen Storage Disease Type III 8 coordinate concepts ∟ Glycogen Storage Disease Type I \| ∟ Glycogen Storage Disease Type II \| ∟ Glycogen Storage Disease Type IIb \| ∟ Glycogen Storage Disease Type IV \| ∟ Glycogen Storage Disease Type V \| ∟ Glycogen Storage Disease Type VI \| ∟ Glycogen Storage Disease Type VII \| ∟ Glycogen Storage Disease Type VIII Medical Subject Headings (MeSH) ∟ Nutritional and Metabolic Diseases ∟ Metabolic Diseases ∟ Metabolism, Inborn Errors ∟ Carbohydrate Metabolism, Inborn Errors ∟ Glycogen Storage Disease ∟ Glycogen Storage Disease Type III 8 coordinate concepts ∟ Glycogen Storage Disease Type I \| ∟ Glycogen Storage Disease Type II \| ∟ Glycogen Storage Disease Type IIb \| ∟ Glycogen Storage Disease Type IV \| ∟ Glycogen Storage Disease Type V \| ∟ Glycogen Storage Disease Type VI \| ∟ Glycogen Storage Disease Type VII \| ∟ Glycogen Storage Disease Type VIII X
Broader terms:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Metabolism, Inborn Errors ∟ Carbohydrate Metabolism, Inborn Errors ∟ Glycogen Storage Disease ∟ Glycogen Storage Disease Type III Medical Subject Headings (MeSH) ∟ Nutritional and Metabolic Diseases ∟ Metabolic Diseases ∟ Metabolism, Inborn Errors ∟ Carbohydrate Metabolism, Inborn Errors ∟ Glycogen Storage Disease ∟ Glycogen Storage Disease Type III Glycogen Storage Disease > Carbohydrate Metabolism, Inborn Errors > Metabolism, Inborn Errors > Genetic Diseases, Inborn > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Medical Subject Headings (MeSH) Glycogen Storage Disease > Carbohydrate Metabolism, Inborn Errors > Metabolism, Inborn Errors > Metabolic Diseases > Nutritional and Metabolic Diseases > Medical Subject Headings (MeSH) X
Annotation:	do not use /congen & do not coord with INFANT, NEWBORN, DISEASES X
History note:	Glucosidases/metabolism (1966-1974) \| Glycogenosis (1966-1974) \| Liver Diseases (1966-1974)X
historyNote*:	91(89); was see under GLYCOGEN STORAGE DISEASE 1989-90; was GLYCOGENOSIS 3 see under GLYCOGENOSIS 1975-88 X
onlineNote*:	use GLYCOGEN STORAGE DISEASE TYPE III to search GLYCOGENOSIS 3 1975-88 X
publicMeSHNote*:	91; was see under GLYCOGEN STORAGE DISEASE 1989-90; was GLYCOGENOSIS 3 see under GLYCOGENOSIS 1975-88 X
Scope note:	An autosomal recessive metabolic disorder due to deficient expression of amylo-1,6-glucosidase (one part of the glycogen debranching enzyme system). The clinical course of the disease is similar to that of glycogen storage disease type I, but milder. Massive hepatomegaly, which is present in young children, diminishes and occasionally disappears with age. Levels of glycogen with short outer branches are elevated in muscle, liver, and erythrocytes. Six subgroups have been identified, with subgroups Type IIIa and Type IIIb being the most prevalent. X
activeMeSHYear*:	2007X
dateCreated*:	1974-12-12X
dateEstablished*:	1991-01-01X
dateRevised*:	2006-07-05X
recordAuthorizer*:	sjnX
recordMaintainer*:	lktX
recordOriginator*:	NLMX
Type:	Concept X
Coordinate terms:	Glycogen Storage Disease Type I \| Glycogen Storage Disease Type II \| Glycogen Storage Disease Type IIb \| Glycogen Storage Disease Type IV \| Glycogen Storage Disease Type V \| Glycogen Storage Disease Type VI \| Glycogen Storage Disease Type VII \| Glycogen Storage Disease Type VIII X
URI:	X
Labels and equivalent concepts:	Glykogenoosi III (fi) Tyypin III dekstrinoosi (fi, replaced) Glykogenoosi tyyppi III (fi, replaced) Dekstrinoosi tyyppi III (fi, replaced) Tyypin III glykogenoosi (fi, replaced) Tyyppi III dekstrinoosi (fi, replaced) Tyyppi III glykogenoosi (fi, replaced) Dekstrinoosi III (fi, replaced) Corin tauti (fi, replaced) Glykogenupplagringssjukdom typ III (sv) Glykogenos 3 (sv, replaced) Deficiency, Debrancher (en, replaced) Debrancher Deficiency (en, replaced) Cori's Disease (en, replaced) Forbes Disease (en, replaced) Glycogen Debranching Enzyme Deficiency (en, replaced) Limit Dextrinosis (en, replaced) Glycogenosis 3 (en, replaced) Cori Disease (en, replaced) Morbus Cor (la-FI, replaced) X
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