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Mucopolysaccharidosis 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 ∟ Mucopolysaccharidoses ∟ Mucopolysaccharidosis III 5 coordinate concepts ∟ Mucopolysaccharidosis I \| ∟ Mucopolysaccharidosis II \| ∟ Mucopolysaccharidosis IV \| ∟ Mucopolysaccharidosis VI \| ∟ Mucopolysaccharidosis VII Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Metabolism, Inborn Errors ∟ Lysosomal Storage Diseases ∟ Mucopolysaccharidoses ∟ Mucopolysaccharidosis III 5 coordinate concepts ∟ Mucopolysaccharidosis I \| ∟ Mucopolysaccharidosis II \| ∟ Mucopolysaccharidosis IV \| ∟ Mucopolysaccharidosis VI \| ∟ Mucopolysaccharidosis VII Medical Subject Headings (MeSH) ∟ Nutritional and Metabolic Diseases ∟ Metabolic Diseases ∟ Metabolism, Inborn Errors ∟ Carbohydrate Metabolism, Inborn Errors ∟ Mucopolysaccharidoses ∟ Mucopolysaccharidosis III 5 coordinate concepts ∟ Mucopolysaccharidosis I \| ∟ Mucopolysaccharidosis II \| ∟ Mucopolysaccharidosis IV \| ∟ Mucopolysaccharidosis VI \| ∟ Mucopolysaccharidosis VII Medical Subject Headings (MeSH) ∟ Nutritional and Metabolic Diseases ∟ Metabolic Diseases ∟ Metabolism, Inborn Errors ∟ Lysosomal Storage Diseases ∟ Mucopolysaccharidoses ∟ Mucopolysaccharidosis III 5 coordinate concepts ∟ Mucopolysaccharidosis I \| ∟ Mucopolysaccharidosis II \| ∟ Mucopolysaccharidosis IV \| ∟ Mucopolysaccharidosis VI \| ∟ Mucopolysaccharidosis VII Medical Subject Headings (MeSH) ∟ Skin and Connective Tissue Diseases ∟ Connective Tissue Diseases ∟ Mucinoses ∟ Mucopolysaccharidoses ∟ Mucopolysaccharidosis III 5 coordinate concepts ∟ Mucopolysaccharidosis I \| ∟ Mucopolysaccharidosis II \| ∟ Mucopolysaccharidosis IV \| ∟ Mucopolysaccharidosis VI \| ∟ Mucopolysaccharidosis VII 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 III Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Metabolism, Inborn Errors ∟ Lysosomal Storage Diseases ∟ Mucopolysaccharidoses ∟ Mucopolysaccharidosis III Medical Subject Headings (MeSH) ∟ Nutritional and Metabolic Diseases ∟ Metabolic Diseases ∟ Metabolism, Inborn Errors ∟ Carbohydrate Metabolism, Inborn Errors ∟ Mucopolysaccharidoses ∟ Mucopolysaccharidosis III Medical Subject Headings (MeSH) ∟ Nutritional and Metabolic Diseases ∟ Metabolic Diseases ∟ Metabolism, Inborn Errors ∟ Lysosomal Storage Diseases ∟ Mucopolysaccharidoses ∟ Mucopolysaccharidosis III Medical Subject Headings (MeSH) ∟ Skin and Connective Tissue Diseases ∟ Connective Tissue Diseases ∟ Mucinoses ∟ Mucopolysaccharidoses ∟ Mucopolysaccharidosis III 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 III X
History note:	Carbohydrate Metabolism, Inborn Errors (1966-1976) \| Mental Retardation (1966-1976) \| Mucopolysaccharides/metabolism (1966-1974) \| Mucopolysaccharidosis (1974)X
historyNote*:	92; was MUCOPOLYSACCHARIDOSIS 3 1991; was see under MUCOPOLYSACCHARIDOSIS 1975-90 X
onlineNote*:	use MUCOPOLYSACCHARIDOSIS III to search MUCOPOLYSACCHARIDOSIS 3 1975-91 X
publicMeSHNote*:	92; was MUCOPOLYSACCHARIDOSIS 3 1991; was see under MUCOPOLYSACCHARIDOSIS 1975-90 X
Scope note:	Mucopolysaccharidosis characterized by heparitin sulfate in the urine, progressive mental retardation, mild dwarfism, and other skeletal disorders. There are four clinically indistinguishable but biochemically distinct forms, each due to a deficiency of a different enzyme. 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:	Mucopolysaccharidosis I \| Mucopolysaccharidosis II \| Mucopolysaccharidosis IV \| Mucopolysaccharidosis VI \| Mucopolysaccharidosis VII X
URI:	X
Labels and equivalent concepts:	Mukopolysakkaridoosi III (fi) Mukopolysackaridos III (sv) MPS III (sv, replaced) Sanfilippos syndrom (sv, replaced) Sanfilippo's Syndrome (en, replaced) Polydystrophic Oligophrenia (en, replaced) San Filippo's Syndrome (en, replaced) Mucopolysaccharidosis 3 (en, replaced) Mucopolysaccharidosis III (la-FI, replaced) X
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