ONKI3 | Medical Subject Headings

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Lysosomal Storage Diseases, Nervous System

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Hierarchy:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Metabolism, Inborn Errors ∟ Brain Diseases, Metabolic, Inborn ∟ Lysosomal Storage Diseases, Nervous System 27 coordinate concepts 5 subordinate concepts ∟ Fucosidosis \| ∟ Glycogen Storage Disease Type II \| ∟ Mucolipidoses \| ∟ Sialic Acid Storage Disease \| ∟ Sphingolipidoses ∟ Carbamoyl-Phosphate Synthase I Deficiency Disease \| ∟ Cerebral Amyloid Angiopathy, Familial \| ∟ Citrullinemia \| ∟ Galactosemias \| ∟ Hartnup Disease \| ∟ Hepatolenticular Degeneration \| ∟ Homocystinuria \| ∟ Hyperargininemia \| ∟ Hyperglycinemia, Nonketotic \| ∟ Hyperlysinemias \| ∟ Leigh Disease \| ∟ Lesch-Nyhan Syndrome \| ∟ Maple Syrup Urine Disease \| ∟ MELAS Syndrome \| ∟ Menkes Kinky Hair Syndrome \| ∟ MERRF Syndrome \| ∟ Oculocerebrorenal Syndrome \| ∟ Ornithine Carbamoyltransferase Deficiency Disease \| ∟ Peroxisomal Disorders \| ∟ Phenylketonurias \| ∟ Pyruvate Carboxylase Deficiency Disease \| ∟ Pyruvate Dehydrogenase Complex Deficiency Disease \| ∟ Tyrosinemias \| ∟ Cholesterol Ester Storage Disease \| ∟ Cystinosis \| ∟ Mannosidase Deficiency Diseases \| ∟ Mucopolysaccharidoses Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Metabolism, Inborn Errors ∟ Lysosomal Storage Diseases ∟ Lysosomal Storage Diseases, Nervous System 27 coordinate concepts 5 subordinate concepts ∟ Fucosidosis \| ∟ Glycogen Storage Disease Type II \| ∟ Mucolipidoses \| ∟ Sialic Acid Storage Disease \| ∟ Sphingolipidoses ∟ Carbamoyl-Phosphate Synthase I Deficiency Disease \| ∟ Cerebral Amyloid Angiopathy, Familial \| ∟ Citrullinemia \| ∟ Galactosemias \| ∟ Hartnup Disease \| ∟ Hepatolenticular Degeneration \| ∟ Homocystinuria \| ∟ Hyperargininemia \| ∟ Hyperglycinemia, Nonketotic \| ∟ Hyperlysinemias \| ∟ Leigh Disease \| ∟ Lesch-Nyhan Syndrome \| ∟ Maple Syrup Urine Disease \| ∟ MELAS Syndrome \| ∟ Menkes Kinky Hair Syndrome \| ∟ MERRF Syndrome \| ∟ Oculocerebrorenal Syndrome \| ∟ Ornithine Carbamoyltransferase Deficiency Disease \| ∟ Peroxisomal Disorders \| ∟ Phenylketonurias \| ∟ Pyruvate Carboxylase Deficiency Disease \| ∟ Pyruvate Dehydrogenase Complex Deficiency Disease \| ∟ Tyrosinemias \| ∟ Cholesterol Ester Storage Disease \| ∟ Cystinosis \| ∟ Mannosidase Deficiency Diseases \| ∟ Mucopolysaccharidoses Medical Subject Headings (MeSH) ∟ Nervous System Diseases ∟ Central Nervous System Diseases ∟ Brain Diseases ∟ Brain Diseases, Metabolic ∟ Brain Diseases, Metabolic, Inborn ∟ Lysosomal Storage Diseases, Nervous System 27 coordinate concepts 5 subordinate concepts ∟ Fucosidosis \| ∟ Glycogen Storage Disease Type II \| ∟ Mucolipidoses \| ∟ Sialic Acid Storage Disease \| ∟ Sphingolipidoses ∟ Carbamoyl-Phosphate Synthase I Deficiency Disease \| ∟ Cerebral Amyloid Angiopathy, Familial \| ∟ Citrullinemia \| ∟ Galactosemias \| ∟ Hartnup Disease \| ∟ Hepatolenticular Degeneration \| ∟ Homocystinuria \| ∟ Hyperargininemia \| ∟ Hyperglycinemia, Nonketotic \| ∟ Hyperlysinemias \| ∟ Leigh Disease \| ∟ Lesch-Nyhan Syndrome \| ∟ Maple Syrup Urine Disease \| ∟ MELAS Syndrome \| ∟ Menkes Kinky Hair Syndrome \| ∟ MERRF Syndrome \| ∟ Oculocerebrorenal Syndrome \| ∟ Ornithine Carbamoyltransferase Deficiency Disease \| ∟ Peroxisomal Disorders \| ∟ Phenylketonurias \| ∟ Pyruvate Carboxylase Deficiency Disease \| ∟ Pyruvate Dehydrogenase Complex Deficiency Disease \| ∟ Tyrosinemias \| ∟ Cholesterol Ester Storage Disease \| ∟ Cystinosis \| ∟ Mannosidase Deficiency Diseases \| ∟ Mucopolysaccharidoses Medical Subject Headings (MeSH) ∟ Nutritional and Metabolic Diseases ∟ Metabolic Diseases ∟ Brain Diseases, Metabolic ∟ Brain Diseases, Metabolic, Inborn ∟ Lysosomal Storage Diseases, Nervous System 27 coordinate concepts 5 subordinate concepts ∟ Fucosidosis \| ∟ Glycogen Storage Disease Type II \| ∟ Mucolipidoses \| ∟ Sialic Acid Storage Disease \| ∟ Sphingolipidoses ∟ Carbamoyl-Phosphate Synthase I Deficiency Disease \| ∟ Cerebral Amyloid Angiopathy, Familial \| ∟ Citrullinemia \| ∟ Galactosemias \| ∟ Hartnup Disease \| ∟ Hepatolenticular Degeneration \| ∟ Homocystinuria \| ∟ Hyperargininemia \| ∟ Hyperglycinemia, Nonketotic \| ∟ Hyperlysinemias \| ∟ Leigh Disease \| ∟ Lesch-Nyhan Syndrome \| ∟ Maple Syrup Urine Disease \| ∟ MELAS Syndrome \| ∟ Menkes Kinky Hair Syndrome \| ∟ MERRF Syndrome \| ∟ Oculocerebrorenal Syndrome \| ∟ Ornithine Carbamoyltransferase Deficiency Disease \| ∟ Peroxisomal Disorders \| ∟ Phenylketonurias \| ∟ Pyruvate Carboxylase Deficiency Disease \| ∟ Pyruvate Dehydrogenase Complex Deficiency Disease \| ∟ Tyrosinemias \| ∟ Cholesterol Ester Storage Disease \| ∟ Cystinosis \| ∟ Mannosidase Deficiency Diseases \| ∟ Mucopolysaccharidoses Medical Subject Headings (MeSH) ∟ Nutritional and Metabolic Diseases ∟ Metabolic Diseases ∟ Metabolism, Inborn Errors ∟ Brain Diseases, Metabolic, Inborn ∟ Lysosomal Storage Diseases, Nervous System 27 coordinate concepts 5 subordinate concepts ∟ Fucosidosis \| ∟ Glycogen Storage Disease Type II \| ∟ Mucolipidoses \| ∟ Sialic Acid Storage Disease \| ∟ Sphingolipidoses ∟ Carbamoyl-Phosphate Synthase I Deficiency Disease \| ∟ Cerebral Amyloid Angiopathy, Familial \| ∟ Citrullinemia \| ∟ Galactosemias \| ∟ Hartnup Disease \| ∟ Hepatolenticular Degeneration \| ∟ Homocystinuria \| ∟ Hyperargininemia \| ∟ Hyperglycinemia, Nonketotic \| ∟ Hyperlysinemias \| ∟ Leigh Disease \| ∟ Lesch-Nyhan Syndrome \| ∟ Maple Syrup Urine Disease \| ∟ MELAS Syndrome \| ∟ Menkes Kinky Hair Syndrome \| ∟ MERRF Syndrome \| ∟ Oculocerebrorenal Syndrome \| ∟ Ornithine Carbamoyltransferase Deficiency Disease \| ∟ Peroxisomal Disorders \| ∟ Phenylketonurias \| ∟ Pyruvate Carboxylase Deficiency Disease \| ∟ Pyruvate Dehydrogenase Complex Deficiency Disease \| ∟ Tyrosinemias \| ∟ Cholesterol Ester Storage Disease \| ∟ Cystinosis \| ∟ Mannosidase Deficiency Diseases \| ∟ Mucopolysaccharidoses Medical Subject Headings (MeSH) ∟ Nutritional and Metabolic Diseases ∟ Metabolic Diseases ∟ Metabolism, Inborn Errors ∟ Lysosomal Storage Diseases ∟ Lysosomal Storage Diseases, Nervous System 27 coordinate concepts 5 subordinate concepts ∟ Fucosidosis \| ∟ Glycogen Storage Disease Type II \| ∟ Mucolipidoses \| ∟ Sialic Acid Storage Disease \| ∟ Sphingolipidoses ∟ Carbamoyl-Phosphate Synthase I Deficiency Disease \| ∟ Cerebral Amyloid Angiopathy, Familial \| ∟ Citrullinemia \| ∟ Galactosemias \| ∟ Hartnup Disease \| ∟ Hepatolenticular Degeneration \| ∟ Homocystinuria \| ∟ Hyperargininemia \| ∟ Hyperglycinemia, Nonketotic \| ∟ Hyperlysinemias \| ∟ Leigh Disease \| ∟ Lesch-Nyhan Syndrome \| ∟ Maple Syrup Urine Disease \| ∟ MELAS Syndrome \| ∟ Menkes Kinky Hair Syndrome \| ∟ MERRF Syndrome \| ∟ Oculocerebrorenal Syndrome \| ∟ Ornithine Carbamoyltransferase Deficiency Disease \| ∟ Peroxisomal Disorders \| ∟ Phenylketonurias \| ∟ Pyruvate Carboxylase Deficiency Disease \| ∟ Pyruvate Dehydrogenase Complex Deficiency Disease \| ∟ Tyrosinemias \| ∟ Cholesterol Ester Storage Disease \| ∟ Cystinosis \| ∟ Mannosidase Deficiency Diseases \| ∟ Mucopolysaccharidoses X
Broader terms:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Metabolism, Inborn Errors ∟ Brain Diseases, Metabolic, Inborn ∟ Lysosomal Storage Diseases, Nervous System Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Metabolism, Inborn Errors ∟ Lysosomal Storage Diseases ∟ Lysosomal Storage Diseases, Nervous System Medical Subject Headings (MeSH) ∟ Nervous System Diseases ∟ Central Nervous System Diseases ∟ Brain Diseases ∟ Brain Diseases, Metabolic ∟ Brain Diseases, Metabolic, Inborn ∟ Lysosomal Storage Diseases, Nervous System Medical Subject Headings (MeSH) ∟ Nutritional and Metabolic Diseases ∟ Metabolic Diseases ∟ Brain Diseases, Metabolic ∟ Brain Diseases, Metabolic, Inborn ∟ Lysosomal Storage Diseases, Nervous System Medical Subject Headings (MeSH) ∟ Nutritional and Metabolic Diseases ∟ Metabolic Diseases ∟ Metabolism, Inborn Errors ∟ Brain Diseases, Metabolic, Inborn ∟ Lysosomal Storage Diseases, Nervous System Medical Subject Headings (MeSH) ∟ Nutritional and Metabolic Diseases ∟ Metabolic Diseases ∟ Metabolism, Inborn Errors ∟ Lysosomal Storage Diseases ∟ Lysosomal Storage Diseases, Nervous System Brain Diseases, Metabolic, Inborn > 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) Brain Diseases, Metabolic, Inborn > Brain Diseases, Metabolic > Brain Diseases > Central Nervous System Diseases > Nervous System Diseases > Medical Subject Headings (MeSH) Brain Diseases, Metabolic, Inborn > Brain Diseases, Metabolic > Metabolic Diseases > Nutritional and Metabolic Diseases > Medical Subject Headings (MeSH) Brain Diseases, Metabolic, Inborn > 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:	Fucosidosis \| Glycogen Storage Disease Type II \| Mucolipidoses \| Sialic Acid Storage Disease \| Sphingolipidoses X
Annotation:	GEN: prefer specifics X
History note:	Brain Diseases (1964-1999) \| Lysosomal Storage Diseases (1992-1999) \| Lysosomes (1964-1999) \| Sphingolipidoses (1974-1999)X
historyNote*:	2000 X
publicMeSHNote*:	2000 X
Scope note:	A group of enzymatic disorders affecting the nervous system and to a variable degree the skeletal system, lymphoreticular system, and other organs. The conditions are marked by an abnormal accumulation of catabolic material within lysosomes. X
activeMeSHYear*:	2007X
dateCreated*:	1999-11-03X
dateEstablished*:	2000-01-01X
dateRevised*:	2006-07-05X
recordAuthorizer*:	sjnX
recordMaintainer*:	lktX
recordOriginator*:	KEVX
Type:	Concept X
Coordinate terms:	Carbamoyl-Phosphate Synthase I Deficiency Disease \| Cerebral Amyloid Angiopathy, Familial \| Citrullinemia \| Galactosemias \| Hartnup Disease \| Hepatolenticular Degeneration \| Homocystinuria \| Hyperargininemia \| Hyperglycinemia, Nonketotic \| Hyperlysinemias \| Leigh Disease \| Lesch-Nyhan Syndrome \| Maple Syrup Urine Disease \| MELAS Syndrome \| Menkes Kinky Hair Syndrome \| MERRF Syndrome \| Oculocerebrorenal Syndrome \| Ornithine Carbamoyltransferase Deficiency Disease \| Peroxisomal Disorders \| Phenylketonurias \| Pyruvate Carboxylase Deficiency Disease \| Pyruvate Dehydrogenase Complex Deficiency Disease \| Tyrosinemias \| Cholesterol Ester Storage Disease \| Cystinosis \| Mannosidase Deficiency Diseases \| Mucopolysaccharidoses X
URI:	X
Labels and equivalent concepts:	Hermoston lysosomaaliset varastoitumissairaudet (fi) Hermoston lysosomaaliset varastoitumistaudit (fi, replaced) Nervous System Lysosomal Storage Diseases (en, replaced) Nervous System Lysosomal Enzyme Disorders (en, replaced) Lysosomal Enzyme Disorders, Nervous System (en, replaced) X
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