ONKI3 | Medical Subject Headings

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Mannosidase Deficiency Diseases

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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 ∟ Mannosidase Deficiency Diseases 15 coordinate concepts 2 subordinate concepts ∟ alpha-Mannosidosis \| ∟ beta-Mannosidosis ∟ Cholesterol Ester Storage Disease \| ∟ Cystinosis \| ∟ Lysosomal Storage Diseases, Nervous System \| ∟ Mucopolysaccharidoses \| ∟ 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 ∟ Mannosidase Deficiency Diseases 15 coordinate concepts 2 subordinate concepts ∟ alpha-Mannosidosis \| ∟ beta-Mannosidosis ∟ Cholesterol Ester Storage Disease \| ∟ Cystinosis \| ∟ Lysosomal Storage Diseases, Nervous System \| ∟ Mucopolysaccharidoses \| ∟ 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 ∟ Mannosidase Deficiency Diseases 15 coordinate concepts 2 subordinate concepts ∟ alpha-Mannosidosis \| ∟ beta-Mannosidosis ∟ Cholesterol Ester Storage Disease \| ∟ Cystinosis \| ∟ Lysosomal Storage Diseases, Nervous System \| ∟ Mucopolysaccharidoses \| ∟ 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 ∟ Mannosidase Deficiency Diseases 15 coordinate concepts 2 subordinate concepts ∟ alpha-Mannosidosis \| ∟ beta-Mannosidosis ∟ Cholesterol Ester Storage Disease \| ∟ Cystinosis \| ∟ Lysosomal Storage Diseases, Nervous System \| ∟ Mucopolysaccharidoses \| ∟ 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 ∟ Mannosidase Deficiency Diseases Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Metabolism, Inborn Errors ∟ Lysosomal Storage Diseases ∟ Mannosidase Deficiency Diseases Medical Subject Headings (MeSH) ∟ Nutritional and Metabolic Diseases ∟ Metabolic Diseases ∟ Metabolism, Inborn Errors ∟ Carbohydrate Metabolism, Inborn Errors ∟ Mannosidase Deficiency Diseases Medical Subject Headings (MeSH) ∟ Nutritional and Metabolic Diseases ∟ Metabolic Diseases ∟ Metabolism, Inborn Errors ∟ Lysosomal Storage Diseases ∟ Mannosidase Deficiency Diseases 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) X
Narrower terms:	alpha-Mannosidosis \| beta-Mannosidosis X
History note:	Mannosidosis (1984-2003)X
historyNote*:	2004; use MANNOSIDOSIS, ALPHA B, LYSOSOMAL 1984-2003 X
publicMeSHNote*:	2004; see MANNOSIDOSIS 1984-2003 X
Scope note:	Diseases caused by the loss of one or more enzymes involved in the hydrolysis of mannoside linkages (MANNOSIDASES). The defects in enzyme activity are primarily associated with genetic mutation of the genes that codes for a particular mannosidase isoenzyme. X
activeMeSHYear*:	2007X
dateCreated*:	2003-07-09X
dateEstablished*:	2004-01-01X
dateRevised*:	2006-07-05X
recordAuthorizer*:	sjnX
recordMaintainer*:	lktX
recordOriginator*:	jmpX
Related term:	Mannosidases X
Type:	Concept X
Coordinate terms:	Cholesterol Ester Storage Disease \| Cystinosis \| Lysosomal Storage Diseases, Nervous System \| Mucopolysaccharidoses \| 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:	Mannosidoosit (fi) Mannosidaasipuutossairaus (fi, replaced) Mannosidoosi (fi, replaced) Mannosidaasipuutossairaudet (fi, replaced) Mannosidaasipuutesairaus (fi, replaced) Mannosidaasipuutesairaudet (fi, replaced) Mannosidasbristsjukdomar (sv) Mannosidos (sv, replaced) Mannosidosis (en, replaced) Mannosidase Deficiency Syndromes (en, replaced) X
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