ONKI3 | Medical Subject Headings

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Mucopolysaccharidosis 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 ∟ Mucopolysaccharidoses ∟ Mucopolysaccharidosis VII 5 coordinate concepts ∟ Mucopolysaccharidosis I \| ∟ Mucopolysaccharidosis II \| ∟ Mucopolysaccharidosis III \| ∟ Mucopolysaccharidosis IV \| ∟ Mucopolysaccharidosis VI Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Metabolism, Inborn Errors ∟ Lysosomal Storage Diseases ∟ Mucopolysaccharidoses ∟ Mucopolysaccharidosis VII 5 coordinate concepts ∟ Mucopolysaccharidosis I \| ∟ Mucopolysaccharidosis II \| ∟ Mucopolysaccharidosis III \| ∟ Mucopolysaccharidosis IV \| ∟ Mucopolysaccharidosis VI Medical Subject Headings (MeSH) ∟ Nutritional and Metabolic Diseases ∟ Metabolic Diseases ∟ Metabolism, Inborn Errors ∟ Carbohydrate Metabolism, Inborn Errors ∟ Mucopolysaccharidoses ∟ Mucopolysaccharidosis VII 5 coordinate concepts ∟ Mucopolysaccharidosis I \| ∟ Mucopolysaccharidosis II \| ∟ Mucopolysaccharidosis III \| ∟ Mucopolysaccharidosis IV \| ∟ Mucopolysaccharidosis VI Medical Subject Headings (MeSH) ∟ Nutritional and Metabolic Diseases ∟ Metabolic Diseases ∟ Metabolism, Inborn Errors ∟ Lysosomal Storage Diseases ∟ Mucopolysaccharidoses ∟ Mucopolysaccharidosis VII 5 coordinate concepts ∟ Mucopolysaccharidosis I \| ∟ Mucopolysaccharidosis II \| ∟ Mucopolysaccharidosis III \| ∟ Mucopolysaccharidosis IV \| ∟ Mucopolysaccharidosis VI Medical Subject Headings (MeSH) ∟ Skin and Connective Tissue Diseases ∟ Connective Tissue Diseases ∟ Mucinoses ∟ Mucopolysaccharidoses ∟ Mucopolysaccharidosis VII 5 coordinate concepts ∟ Mucopolysaccharidosis I \| ∟ Mucopolysaccharidosis II \| ∟ Mucopolysaccharidosis III \| ∟ Mucopolysaccharidosis IV \| ∟ Mucopolysaccharidosis VI X
Broader terms:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Metabolism, Inborn Errors ∟ Carbohydrate Metabolism, Inborn Errors ∟ Mucopolysaccharidoses ∟ Mucopolysaccharidosis VII Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Metabolism, Inborn Errors ∟ Lysosomal Storage Diseases ∟ Mucopolysaccharidoses ∟ Mucopolysaccharidosis VII Medical Subject Headings (MeSH) ∟ Nutritional and Metabolic Diseases ∟ Metabolic Diseases ∟ Metabolism, Inborn Errors ∟ Carbohydrate Metabolism, Inborn Errors ∟ Mucopolysaccharidoses ∟ Mucopolysaccharidosis VII Medical Subject Headings (MeSH) ∟ Nutritional and Metabolic Diseases ∟ Metabolic Diseases ∟ Metabolism, Inborn Errors ∟ Lysosomal Storage Diseases ∟ Mucopolysaccharidoses ∟ Mucopolysaccharidosis VII Medical Subject Headings (MeSH) ∟ Skin and Connective Tissue Diseases ∟ Connective Tissue Diseases ∟ Mucinoses ∟ Mucopolysaccharidoses ∟ Mucopolysaccharidosis VII Mucopolysaccharidoses > Carbohydrate Metabolism, Inborn Errors > Metabolism, Inborn Errors > Genetic Diseases, Inborn > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Medical Subject Headings (MeSH) Mucopolysaccharidoses > Lysosomal Storage Diseases > Metabolism, Inborn Errors > Genetic Diseases, Inborn > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Medical Subject Headings (MeSH) Mucopolysaccharidoses > Carbohydrate Metabolism, Inborn Errors > Metabolism, Inborn Errors > Metabolic Diseases > Nutritional and Metabolic Diseases > Medical Subject Headings (MeSH) Mucopolysaccharidoses > Lysosomal Storage Diseases > Metabolism, Inborn Errors > Metabolic Diseases > Nutritional and Metabolic Diseases > Medical Subject Headings (MeSH) Mucopolysaccharidoses > Mucinoses > Connective Tissue Diseases > Skin and Connective Tissue Diseases > Medical Subject Headings (MeSH) X
Annotation:	do not use /congen & do not coord with INFANT, NEWBORN, DISEASES; DF: MPS VII X
History note:	Mucopolysaccharidoses (1974-1991)X
historyNote*:	92 X
publicMeSHNote*:	92 X
Scope note:	Mucopolysaccharidosis characterized by excessive dermatan and heparan sulfates in the urine and Hurler-like features. It is caused by a deficiency of beta-glucuronidase. X
activeMeSHYear*:	2007X
dateCreated*:	1991-06-21X
dateEstablished*:	1992-01-01X
dateRevised*:	2006-07-05X
recordAuthorizer*:	sjnX
recordMaintainer*:	lktX
recordOriginator*:	AGSX
Type:	Concept X
Coordinate terms:	Mucopolysaccharidosis I \| Mucopolysaccharidosis II \| Mucopolysaccharidosis III \| Mucopolysaccharidosis IV \| Mucopolysaccharidosis VI X
URI:	X
Labels and equivalent concepts:	Mukopolysakkaridoosi VII (fi) Mukopolysackaridos VII (sv) Slys syndrom (sv, replaced) Sly Syndrome (en, replaced) Sly Disease (en, replaced) Mucopolysaccharidosis 7 (en, replaced) Mucopolysaccharidosis VII (la-FI, replaced) X
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