ONKI3 | Medical Subject Headings

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Glycogen Storage Disease Type VII

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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 VII 16 coordinate concepts ∟ Glycogen Storage Disease Type I \| ∟ Glycogen Storage Disease Type II \| ∟ Glycogen Storage Disease Type IIb \| ∟ Glycogen Storage Disease Type III \| ∟ Glycogen Storage Disease Type IV \| ∟ Glycogen Storage Disease Type V \| ∟ Glycogen Storage Disease Type VI \| ∟ Glycogen Storage Disease Type VIII \| ∟ D009136Q000662* \| ∟ Distal Myopathies \| ∟ Muscular Dystrophies, Limb-Girdle \| ∟ Muscular Dystrophy, Duchenne \| ∟ Muscular Dystrophy, Emery-Dreifuss \| ∟ Muscular Dystrophy, Facioscapulohumeral \| ∟ Muscular Dystrophy, Oculopharyngeal \| ∟ Myotonic Dystrophy Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Muscular Dystrophies ∟ Glycogen Storage Disease Type VII 16 coordinate concepts ∟ Glycogen Storage Disease Type I \| ∟ Glycogen Storage Disease Type II \| ∟ Glycogen Storage Disease Type IIb \| ∟ Glycogen Storage Disease Type III \| ∟ Glycogen Storage Disease Type IV \| ∟ Glycogen Storage Disease Type V \| ∟ Glycogen Storage Disease Type VI \| ∟ Glycogen Storage Disease Type VIII \| ∟ D009136Q000662* \| ∟ Distal Myopathies \| ∟ Muscular Dystrophies, Limb-Girdle \| ∟ Muscular Dystrophy, Duchenne \| ∟ Muscular Dystrophy, Emery-Dreifuss \| ∟ Muscular Dystrophy, Facioscapulohumeral \| ∟ Muscular Dystrophy, Oculopharyngeal \| ∟ Myotonic Dystrophy Medical Subject Headings (MeSH) ∟ Musculoskeletal Diseases ∟ Muscular Diseases ∟ Muscular Disorders, Atrophic ∟ Muscular Dystrophies ∟ Glycogen Storage Disease Type VII 16 coordinate concepts ∟ Glycogen Storage Disease Type I \| ∟ Glycogen Storage Disease Type II \| ∟ Glycogen Storage Disease Type IIb \| ∟ Glycogen Storage Disease Type III \| ∟ Glycogen Storage Disease Type IV \| ∟ Glycogen Storage Disease Type V \| ∟ Glycogen Storage Disease Type VI \| ∟ Glycogen Storage Disease Type VIII \| ∟ D009136Q000662* \| ∟ Distal Myopathies \| ∟ Muscular Dystrophies, Limb-Girdle \| ∟ Muscular Dystrophy, Duchenne \| ∟ Muscular Dystrophy, Emery-Dreifuss \| ∟ Muscular Dystrophy, Facioscapulohumeral \| ∟ Muscular Dystrophy, Oculopharyngeal \| ∟ Myotonic Dystrophy Medical Subject Headings (MeSH) ∟ Nervous System Diseases ∟ Neuromuscular Diseases ∟ Muscular Diseases ∟ Muscular Disorders, Atrophic ∟ Muscular Dystrophies ∟ Glycogen Storage Disease Type VII 16 coordinate concepts ∟ Glycogen Storage Disease Type I \| ∟ Glycogen Storage Disease Type II \| ∟ Glycogen Storage Disease Type IIb \| ∟ Glycogen Storage Disease Type III \| ∟ Glycogen Storage Disease Type IV \| ∟ Glycogen Storage Disease Type V \| ∟ Glycogen Storage Disease Type VI \| ∟ Glycogen Storage Disease Type VIII \| ∟ D009136Q000662* \| ∟ Distal Myopathies \| ∟ Muscular Dystrophies, Limb-Girdle \| ∟ Muscular Dystrophy, Duchenne \| ∟ Muscular Dystrophy, Emery-Dreifuss \| ∟ Muscular Dystrophy, Facioscapulohumeral \| ∟ Muscular Dystrophy, Oculopharyngeal \| ∟ Myotonic Dystrophy Medical Subject Headings (MeSH) ∟ Nervous System Diseases ∟ Neuromuscular Diseases ∟ Muscular Disorders, Atrophic ∟ Muscular Dystrophies ∟ Glycogen Storage Disease Type VII 16 coordinate concepts ∟ Glycogen Storage Disease Type I \| ∟ Glycogen Storage Disease Type II \| ∟ Glycogen Storage Disease Type IIb \| ∟ Glycogen Storage Disease Type III \| ∟ Glycogen Storage Disease Type IV \| ∟ Glycogen Storage Disease Type V \| ∟ Glycogen Storage Disease Type VI \| ∟ Glycogen Storage Disease Type VIII \| ∟ D009136Q000662* \| ∟ Distal Myopathies \| ∟ Muscular Dystrophies, Limb-Girdle \| ∟ Muscular Dystrophy, Duchenne \| ∟ Muscular Dystrophy, Emery-Dreifuss \| ∟ Muscular Dystrophy, Facioscapulohumeral \| ∟ Muscular Dystrophy, Oculopharyngeal \| ∟ Myotonic Dystrophy Medical Subject Headings (MeSH) ∟ Nutritional and Metabolic Diseases ∟ Metabolic Diseases ∟ Metabolism, Inborn Errors ∟ Carbohydrate Metabolism, Inborn Errors ∟ Glycogen Storage Disease ∟ Glycogen Storage Disease Type VII 16 coordinate concepts ∟ Glycogen Storage Disease Type I \| ∟ Glycogen Storage Disease Type II \| ∟ Glycogen Storage Disease Type IIb \| ∟ Glycogen Storage Disease Type III \| ∟ Glycogen Storage Disease Type IV \| ∟ Glycogen Storage Disease Type V \| ∟ Glycogen Storage Disease Type VI \| ∟ Glycogen Storage Disease Type VIII \| ∟ D009136Q000662* \| ∟ Distal Myopathies \| ∟ Muscular Dystrophies, Limb-Girdle \| ∟ Muscular Dystrophy, Duchenne \| ∟ Muscular Dystrophy, Emery-Dreifuss \| ∟ Muscular Dystrophy, Facioscapulohumeral \| ∟ Muscular Dystrophy, Oculopharyngeal \| ∟ Myotonic Dystrophy 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 VII Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Muscular Dystrophies ∟ Glycogen Storage Disease Type VII Medical Subject Headings (MeSH) ∟ Musculoskeletal Diseases ∟ Muscular Diseases ∟ Muscular Disorders, Atrophic ∟ Muscular Dystrophies ∟ Glycogen Storage Disease Type VII Medical Subject Headings (MeSH) ∟ Nervous System Diseases ∟ Neuromuscular Diseases ∟ Muscular Diseases ∟ Muscular Disorders, Atrophic ∟ Muscular Dystrophies ∟ Glycogen Storage Disease Type VII Medical Subject Headings (MeSH) ∟ Nervous System Diseases ∟ Neuromuscular Diseases ∟ Muscular Disorders, Atrophic ∟ Muscular Dystrophies ∟ Glycogen Storage Disease Type VII Medical Subject Headings (MeSH) ∟ Nutritional and Metabolic Diseases ∟ Metabolic Diseases ∟ Metabolism, Inborn Errors ∟ Carbohydrate Metabolism, Inborn Errors ∟ Glycogen Storage Disease ∟ Glycogen Storage Disease Type VII Glycogen Storage Disease > Carbohydrate Metabolism, Inborn Errors > Metabolism, Inborn Errors > Genetic Diseases, Inborn > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Medical Subject Headings (MeSH) Muscular Dystrophies > Genetic Diseases, Inborn > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Medical Subject Headings (MeSH) Muscular Dystrophies > Muscular Disorders, Atrophic > Muscular Diseases > Musculoskeletal Diseases > Medical Subject Headings (MeSH) Muscular Dystrophies > Muscular Disorders, Atrophic > Muscular Diseases > Neuromuscular Diseases > Nervous System Diseases > Medical Subject Headings (MeSH) Muscular Dystrophies > Muscular Disorders, Atrophic > Neuromuscular Diseases > Nervous System Diseases > 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:	Glycogenosis (1966-1974)X
historyNote*:	91(89); was see under GLYCOGEN STORAGE DISEASE 1989-90; was GLYCOGENOSIS 7 see under GLYCOGENOSIS 1975-88 X
onlineNote*:	use GLYCOGEN STORAGE DISEASE TYPE VII to search GLYCOGENOSIS 7 1975-88 X
publicMeSHNote*:	91; was see under GLYCOGEN STORAGE DISEASE 1989-90; was GLYCOGENOSIS 7 see under GLYCOGENOSIS 1975-88 X
Scope note:	An autosomal recessive glycogen storage disease in which there is deficient expression of 6-phosphofructose 1-kinase in muscle (PHOSPHOFRUCTOKINASE-1, MUSCLE TYPE) resulting in abnormal deposition of glycogen in muscle tissue. These patients have severe congenital muscular dystrophy and are exercise intolerant. 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 III \| Glycogen Storage Disease Type IV \| Glycogen Storage Disease Type V \| Glycogen Storage Disease Type VI \| Glycogen Storage Disease Type VIII \| D009136Q000662* \| Distal Myopathies \| Muscular Dystrophies, Limb-Girdle \| Muscular Dystrophy, Duchenne \| Muscular Dystrophy, Emery-Dreifuss \| Muscular Dystrophy, Facioscapulohumeral \| Muscular Dystrophy, Oculopharyngeal \| Myotonic Dystrophy X
URI:	X
Labels and equivalent concepts:	Glykogenoosi VII (fi) Tyypin VII glykogenoosi (fi, replaced) Tyypin VII dekstrinoosi (fi, replaced) Tyyppi VII dekstrinoosi (fi, replaced) Tyyppi VII glykogenoosi (fi, replaced) Glykogenoosi tyyppi VII (fi, replaced) Dekstrinoosi VII (fi, replaced) Dekstrinoosi tyyppi VII (fi, replaced) Glykogenupplagringssjukdom typ VII (sv) Glykogenos 7 (sv, replaced) Muscle Phosphofructokinase Deficiency (en, replaced) Glycogenosis 7 (en, replaced) Tarui Disease (en, replaced) Tarui's Disease (en, replaced) Deficiency, Muscle Phosphofructokinase (en, replaced) X
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