ONKI3 | Medical Subject Headings

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Mucopolysaccharidoses

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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 20 coordinate concepts 6 subordinate concepts ∟ Mucopolysaccharidosis I \| ∟ Mucopolysaccharidosis II \| ∟ Mucopolysaccharidosis III \| ∟ Mucopolysaccharidosis IV \| ∟ Mucopolysaccharidosis VI \| ∟ Mucopolysaccharidosis VII ∟ Cholesterol Ester Storage Disease \| ∟ Cystinosis \| ∟ Lysosomal Storage Diseases, Nervous System \| ∟ Mannosidase Deficiency Diseases \| ∟ Ganglion Cysts \| ∟ Mucinosis, Follicular \| ∟ Myxedema \| ∟ Scleredema Adultorum \| ∟ Scleromyxedema \| ∟ Carbohydrate-Deficient Glycoprotein Syndrome \| ∟ Fructose Metabolism, Inborn Errors \| ∟ Fucosidosis \| ∟ Galactosemias \| ∟ Glucosephosphate Dehydrogenase Deficiency \| ∟ Glycogen Storage Disease \| ∟ Hyperoxaluria, Primary \| ∟ Lactose Intolerance \| ∟ Mucolipidoses \| ∟ Multiple Carboxylase Deficiency \| ∟ Pyruvate Metabolism, Inborn Errors Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Metabolism, Inborn Errors ∟ Lysosomal Storage Diseases ∟ Mucopolysaccharidoses 20 coordinate concepts 6 subordinate concepts ∟ Mucopolysaccharidosis I \| ∟ Mucopolysaccharidosis II \| ∟ Mucopolysaccharidosis III \| ∟ Mucopolysaccharidosis IV \| ∟ Mucopolysaccharidosis VI \| ∟ Mucopolysaccharidosis VII ∟ Cholesterol Ester Storage Disease \| ∟ Cystinosis \| ∟ Lysosomal Storage Diseases, Nervous System \| ∟ Mannosidase Deficiency Diseases \| ∟ Ganglion Cysts \| ∟ Mucinosis, Follicular \| ∟ Myxedema \| ∟ Scleredema Adultorum \| ∟ Scleromyxedema \| ∟ Carbohydrate-Deficient Glycoprotein Syndrome \| ∟ Fructose Metabolism, Inborn Errors \| ∟ Fucosidosis \| ∟ Galactosemias \| ∟ Glucosephosphate Dehydrogenase Deficiency \| ∟ Glycogen Storage Disease \| ∟ Hyperoxaluria, Primary \| ∟ Lactose Intolerance \| ∟ Mucolipidoses \| ∟ Multiple Carboxylase Deficiency \| ∟ Pyruvate Metabolism, Inborn Errors Medical Subject Headings (MeSH) ∟ Nutritional and Metabolic Diseases ∟ Metabolic Diseases ∟ Metabolism, Inborn Errors ∟ Carbohydrate Metabolism, Inborn Errors ∟ Mucopolysaccharidoses 20 coordinate concepts 6 subordinate concepts ∟ Mucopolysaccharidosis I \| ∟ Mucopolysaccharidosis II \| ∟ Mucopolysaccharidosis III \| ∟ Mucopolysaccharidosis IV \| ∟ Mucopolysaccharidosis VI \| ∟ Mucopolysaccharidosis VII ∟ Cholesterol Ester Storage Disease \| ∟ Cystinosis \| ∟ Lysosomal Storage Diseases, Nervous System \| ∟ Mannosidase Deficiency Diseases \| ∟ Ganglion Cysts \| ∟ Mucinosis, Follicular \| ∟ Myxedema \| ∟ Scleredema Adultorum \| ∟ Scleromyxedema \| ∟ Carbohydrate-Deficient Glycoprotein Syndrome \| ∟ Fructose Metabolism, Inborn Errors \| ∟ Fucosidosis \| ∟ Galactosemias \| ∟ Glucosephosphate Dehydrogenase Deficiency \| ∟ Glycogen Storage Disease \| ∟ Hyperoxaluria, Primary \| ∟ Lactose Intolerance \| ∟ Mucolipidoses \| ∟ Multiple Carboxylase Deficiency \| ∟ Pyruvate Metabolism, Inborn Errors Medical Subject Headings (MeSH) ∟ Nutritional and Metabolic Diseases ∟ Metabolic Diseases ∟ Metabolism, Inborn Errors ∟ Lysosomal Storage Diseases ∟ Mucopolysaccharidoses 20 coordinate concepts 6 subordinate concepts ∟ Mucopolysaccharidosis I \| ∟ Mucopolysaccharidosis II \| ∟ Mucopolysaccharidosis III \| ∟ Mucopolysaccharidosis IV \| ∟ Mucopolysaccharidosis VI \| ∟ Mucopolysaccharidosis VII ∟ Cholesterol Ester Storage Disease \| ∟ Cystinosis \| ∟ Lysosomal Storage Diseases, Nervous System \| ∟ Mannosidase Deficiency Diseases \| ∟ Ganglion Cysts \| ∟ Mucinosis, Follicular \| ∟ Myxedema \| ∟ Scleredema Adultorum \| ∟ Scleromyxedema \| ∟ Carbohydrate-Deficient Glycoprotein Syndrome \| ∟ Fructose Metabolism, Inborn Errors \| ∟ Fucosidosis \| ∟ Galactosemias \| ∟ Glucosephosphate Dehydrogenase Deficiency \| ∟ Glycogen Storage Disease \| ∟ Hyperoxaluria, Primary \| ∟ Lactose Intolerance \| ∟ Mucolipidoses \| ∟ Multiple Carboxylase Deficiency \| ∟ Pyruvate Metabolism, Inborn Errors Medical Subject Headings (MeSH) ∟ Skin and Connective Tissue Diseases ∟ Connective Tissue Diseases ∟ Mucinoses ∟ Mucopolysaccharidoses 20 coordinate concepts 6 subordinate concepts ∟ Mucopolysaccharidosis I \| ∟ Mucopolysaccharidosis II \| ∟ Mucopolysaccharidosis III \| ∟ Mucopolysaccharidosis IV \| ∟ Mucopolysaccharidosis VI \| ∟ Mucopolysaccharidosis VII ∟ Cholesterol Ester Storage Disease \| ∟ Cystinosis \| ∟ Lysosomal Storage Diseases, Nervous System \| ∟ Mannosidase Deficiency Diseases \| ∟ Ganglion Cysts \| ∟ Mucinosis, Follicular \| ∟ Myxedema \| ∟ Scleredema Adultorum \| ∟ Scleromyxedema \| ∟ Carbohydrate-Deficient Glycoprotein Syndrome \| ∟ Fructose Metabolism, Inborn Errors \| ∟ Fucosidosis \| ∟ Galactosemias \| ∟ Glucosephosphate Dehydrogenase Deficiency \| ∟ Glycogen Storage Disease \| ∟ Hyperoxaluria, Primary \| ∟ Lactose Intolerance \| ∟ Mucolipidoses \| ∟ Multiple Carboxylase Deficiency \| ∟ Pyruvate Metabolism, Inborn Errors 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 Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Metabolism, Inborn Errors ∟ Lysosomal Storage Diseases ∟ Mucopolysaccharidoses Medical Subject Headings (MeSH) ∟ Nutritional and Metabolic Diseases ∟ Metabolic Diseases ∟ Metabolism, Inborn Errors ∟ Carbohydrate Metabolism, Inborn Errors ∟ Mucopolysaccharidoses Medical Subject Headings (MeSH) ∟ Nutritional and Metabolic Diseases ∟ Metabolic Diseases ∟ Metabolism, Inborn Errors ∟ Lysosomal Storage Diseases ∟ Mucopolysaccharidoses Medical Subject Headings (MeSH) ∟ Skin and Connective Tissue Diseases ∟ Connective Tissue Diseases ∟ Mucinoses ∟ Mucopolysaccharidoses Carbohydrate Metabolism, Inborn Errors > Metabolism, Inborn Errors > Genetic Diseases, Inborn > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Medical Subject Headings (MeSH) Lysosomal Storage Diseases > Metabolism, Inborn Errors > Genetic Diseases, Inborn > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Medical Subject Headings (MeSH) Carbohydrate Metabolism, Inborn Errors > Metabolism, Inborn Errors > Metabolic Diseases > Nutritional and Metabolic Diseases > Medical Subject Headings (MeSH) Lysosomal Storage Diseases > Metabolism, Inborn Errors > Metabolic Diseases > Nutritional and Metabolic Diseases > Medical Subject Headings (MeSH) Mucinoses > Connective Tissue Diseases > Skin and Connective Tissue Diseases > Medical Subject Headings (MeSH) X
Narrower terms:	Mucopolysaccharidosis I \| Mucopolysaccharidosis II \| Mucopolysaccharidosis III \| Mucopolysaccharidosis IV \| Mucopolysaccharidosis VI \| Mucopolysaccharidosis VII X
Annotation:	lysosomal storage dis; types I through VII except V are available as main headings: V = MUCOPOLYSACCHARIDOSIS V see MUCOPOLYSACCHARIDOSIS I; do not use /congen & do not coord with INFANT, NEWBORN, DISEASES X
historyNote*:	92; was MUCOPOLYSACCHARIDOSIS 1974-91 X
onlineNote*:	use MUCOPOLYSACCHARIDOSES to search MUCOPOLYSACCHARIDOSIS 1974-91 X
publicMeSHNote*:	92; was MUCOPOLYSACCHARIDOSIS 1974-91 X
Scope note:	Group of lysosomal storage diseases each caused by an inherited deficiency of an enzyme involved in the degradation of glycosaminoglycans (mucopolysaccharides). The diseases are progressive and often display a wide spectrum of clinical severity within one enzyme deficiency. X
activeMeSHYear*:	2007X
dateCreated*:	1999-01-01X
dateEstablished*:	1974-01-01X
dateRevised*:	2006-07-05X
recordAuthorizer*:	sjnX
recordMaintainer*:	lktX
recordOriginator*:	NLMX
Type:	Concept X
Coordinate terms:	Cholesterol Ester Storage Disease \| Cystinosis \| Lysosomal Storage Diseases, Nervous System \| Mannosidase Deficiency Diseases \| Ganglion Cysts \| Mucinosis, Follicular \| Myxedema \| Scleredema Adultorum \| Scleromyxedema \| Carbohydrate-Deficient Glycoprotein Syndrome \| Fructose Metabolism, Inborn Errors \| Fucosidosis \| Galactosemias \| Glucosephosphate Dehydrogenase Deficiency \| Glycogen Storage Disease \| Hyperoxaluria, Primary \| Lactose Intolerance \| Mucolipidoses \| Multiple Carboxylase Deficiency \| Pyruvate Metabolism, Inborn Errors X
URI:	X
Labels and equivalent concepts:	Mukopolysakkaridoosit (fi) Mukopolysakkaridoosi (fi, replaced) Mukopolysackaridoser (sv) Mukopolysackaridossjukdomar (sv, replaced) MPS-sjukdomar (sv, replaced) Mucopolysaccharidosis (en, replaced) Mucopolysaccharidosis (la-FI, replaced) X
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