ONKI3 | Medical Subject Headings


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 ∟ Sphingolipidoses ∟ Sulfatidosis 6 coordinate concepts 2 subordinate concepts ∟ Leukodystrophy, Metachromatic \| ∟ Multiple Sulfatase Deficiency Disease ∟ Fabry Disease \| ∟ Gangliosidoses \| ∟ Gaucher Disease \| ∟ Leukodystrophy, Globoid Cell \| ∟ Niemann-Pick Diseases \| ∟ Sea-Blue Histiocyte Syndrome Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Metabolism, Inborn Errors ∟ Lipid Metabolism, Inborn Errors ∟ Lipidoses ∟ Sphingolipidoses ∟ Sulfatidosis 6 coordinate concepts 2 subordinate concepts ∟ Leukodystrophy, Metachromatic \| ∟ Multiple Sulfatase Deficiency Disease ∟ Fabry Disease \| ∟ Gangliosidoses \| ∟ Gaucher Disease \| ∟ Leukodystrophy, Globoid Cell \| ∟ Niemann-Pick Diseases \| ∟ Sea-Blue Histiocyte Syndrome 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 ∟ Sphingolipidoses ∟ Sulfatidosis 6 coordinate concepts 2 subordinate concepts ∟ Leukodystrophy, Metachromatic \| ∟ Multiple Sulfatase Deficiency Disease ∟ Fabry Disease \| ∟ Gangliosidoses \| ∟ Gaucher Disease \| ∟ Leukodystrophy, Globoid Cell \| ∟ Niemann-Pick Diseases \| ∟ Sea-Blue Histiocyte Syndrome 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 ∟ Sphingolipidoses ∟ Sulfatidosis 6 coordinate concepts 2 subordinate concepts ∟ Leukodystrophy, Metachromatic \| ∟ Multiple Sulfatase Deficiency Disease ∟ Fabry Disease \| ∟ Gangliosidoses \| ∟ Gaucher Disease \| ∟ Leukodystrophy, Globoid Cell \| ∟ Niemann-Pick Diseases \| ∟ Sea-Blue Histiocyte Syndrome Medical Subject Headings (MeSH) ∟ Nutritional and Metabolic Diseases ∟ Metabolic Diseases ∟ Brain Diseases, Metabolic ∟ Brain Diseases, Metabolic, Inborn ∟ Lysosomal Storage Diseases, Nervous System ∟ Sphingolipidoses ∟ Sulfatidosis 6 coordinate concepts 2 subordinate concepts ∟ Leukodystrophy, Metachromatic \| ∟ Multiple Sulfatase Deficiency Disease ∟ Fabry Disease \| ∟ Gangliosidoses \| ∟ Gaucher Disease \| ∟ Leukodystrophy, Globoid Cell \| ∟ Niemann-Pick Diseases \| ∟ Sea-Blue Histiocyte Syndrome Medical Subject Headings (MeSH) ∟ Nutritional and Metabolic Diseases ∟ Metabolic Diseases ∟ Lipid Metabolism Disorders ∟ Lipidoses ∟ Sphingolipidoses ∟ Sulfatidosis 6 coordinate concepts 2 subordinate concepts ∟ Leukodystrophy, Metachromatic \| ∟ Multiple Sulfatase Deficiency Disease ∟ Fabry Disease \| ∟ Gangliosidoses \| ∟ Gaucher Disease \| ∟ Leukodystrophy, Globoid Cell \| ∟ Niemann-Pick Diseases \| ∟ Sea-Blue Histiocyte Syndrome Medical Subject Headings (MeSH) ∟ Nutritional and Metabolic Diseases ∟ Metabolic Diseases ∟ Metabolism, Inborn Errors ∟ Brain Diseases, Metabolic, Inborn ∟ Lysosomal Storage Diseases, Nervous System ∟ Sphingolipidoses ∟ Sulfatidosis 6 coordinate concepts 2 subordinate concepts ∟ Leukodystrophy, Metachromatic \| ∟ Multiple Sulfatase Deficiency Disease ∟ Fabry Disease \| ∟ Gangliosidoses \| ∟ Gaucher Disease \| ∟ Leukodystrophy, Globoid Cell \| ∟ Niemann-Pick Diseases \| ∟ Sea-Blue Histiocyte Syndrome Medical Subject Headings (MeSH) ∟ Nutritional and Metabolic Diseases ∟ Metabolic Diseases ∟ Metabolism, Inborn Errors ∟ Lipid Metabolism, Inborn Errors ∟ Lipidoses ∟ Sphingolipidoses ∟ Sulfatidosis 6 coordinate concepts 2 subordinate concepts ∟ Leukodystrophy, Metachromatic \| ∟ Multiple Sulfatase Deficiency Disease ∟ Fabry Disease \| ∟ Gangliosidoses \| ∟ Gaucher Disease \| ∟ Leukodystrophy, Globoid Cell \| ∟ Niemann-Pick Diseases \| ∟ Sea-Blue Histiocyte Syndrome Medical Subject Headings (MeSH) ∟ Nutritional and Metabolic Diseases ∟ Metabolic Diseases ∟ Metabolism, Inborn Errors ∟ Lysosomal Storage Diseases ∟ Lysosomal Storage Diseases, Nervous System ∟ Sphingolipidoses ∟ Sulfatidosis 6 coordinate concepts 2 subordinate concepts ∟ Leukodystrophy, Metachromatic \| ∟ Multiple Sulfatase Deficiency Disease ∟ Fabry Disease \| ∟ Gangliosidoses \| ∟ Gaucher Disease \| ∟ Leukodystrophy, Globoid Cell \| ∟ Niemann-Pick Diseases \| ∟ Sea-Blue Histiocyte Syndrome 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 ∟ Sphingolipidoses ∟ Sulfatidosis Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Metabolism, Inborn Errors ∟ Lipid Metabolism, Inborn Errors ∟ Lipidoses ∟ Sphingolipidoses ∟ Sulfatidosis 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 ∟ Sphingolipidoses ∟ Sulfatidosis 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 ∟ Sphingolipidoses ∟ Sulfatidosis Medical Subject Headings (MeSH) ∟ Nutritional and Metabolic Diseases ∟ Metabolic Diseases ∟ Brain Diseases, Metabolic ∟ Brain Diseases, Metabolic, Inborn ∟ Lysosomal Storage Diseases, Nervous System ∟ Sphingolipidoses ∟ Sulfatidosis Medical Subject Headings (MeSH) ∟ Nutritional and Metabolic Diseases ∟ Metabolic Diseases ∟ Lipid Metabolism Disorders ∟ Lipidoses ∟ Sphingolipidoses ∟ Sulfatidosis Medical Subject Headings (MeSH) ∟ Nutritional and Metabolic Diseases ∟ Metabolic Diseases ∟ Metabolism, Inborn Errors ∟ Brain Diseases, Metabolic, Inborn ∟ Lysosomal Storage Diseases, Nervous System ∟ Sphingolipidoses ∟ Sulfatidosis Medical Subject Headings (MeSH) ∟ Nutritional and Metabolic Diseases ∟ Metabolic Diseases ∟ Metabolism, Inborn Errors ∟ Lipid Metabolism, Inborn Errors ∟ Lipidoses ∟ Sphingolipidoses ∟ Sulfatidosis Medical Subject Headings (MeSH) ∟ Nutritional and Metabolic Diseases ∟ Metabolic Diseases ∟ Metabolism, Inborn Errors ∟ Lysosomal Storage Diseases ∟ Lysosomal Storage Diseases, Nervous System ∟ Sphingolipidoses ∟ Sulfatidosis Sphingolipidoses > 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) Sphingolipidoses > Lipidoses > Lipid Metabolism, Inborn Errors > Metabolism, Inborn Errors > Genetic Diseases, Inborn > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Medical Subject Headings (MeSH) Sphingolipidoses > Lysosomal Storage Diseases, Nervous System > Lysosomal Storage Diseases > Metabolism, Inborn Errors > Genetic Diseases, Inborn > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Medical Subject Headings (MeSH) Sphingolipidoses > Lysosomal Storage Diseases, Nervous System > Brain Diseases, Metabolic, Inborn > Brain Diseases, Metabolic > Brain Diseases > Central Nervous System Diseases > Nervous System Diseases > Medical Subject Headings (MeSH) Sphingolipidoses > Lysosomal Storage Diseases, Nervous System > Brain Diseases, Metabolic, Inborn > Brain Diseases, Metabolic > Metabolic Diseases > Nutritional and Metabolic Diseases > Medical Subject Headings (MeSH) Sphingolipidoses > Lipidoses > Lipid Metabolism Disorders > Metabolic Diseases > Nutritional and Metabolic Diseases > Medical Subject Headings (MeSH) Sphingolipidoses > Lysosomal Storage Diseases, Nervous System > Brain Diseases, Metabolic, Inborn > Metabolism, Inborn Errors > Metabolic Diseases > Nutritional and Metabolic Diseases > Medical Subject Headings (MeSH) Sphingolipidoses > Lipidoses > Lipid Metabolism, Inborn Errors > Metabolism, Inborn Errors > Metabolic Diseases > Nutritional and Metabolic Diseases > Medical Subject Headings (MeSH) Sphingolipidoses > Lysosomal Storage Diseases, Nervous System > Lysosomal Storage Diseases > Metabolism, Inborn Errors > Metabolic Diseases > Nutritional and Metabolic Diseases > Medical Subject Headings (MeSH) X
Narrower terms:	Leukodystrophy, Metachromatic \| Multiple Sulfatase Deficiency Disease X
historyNote*:	2007; use LEUKODYSTROPHY, METACHROMATIC 1974-2006 X
publicMeSHNote*:	2007; see LEUKODYSTROPHY, METACHROMATIC 1974-2006 X
Scope note:	A group of inherited metabolic disorders characterized by the intralysosomal accumulation of sulfur-containing lipids (SULFATIDES), including SULFOGLYCOSPHINGOLIPIDS normally found in the MYELIN SHEATH of the brain. These disorders are caused by defective degradative enzymes leading to substrate accumulation (or storage). X
activeMeSHYear*:	2007X
dateCreated*:	2006-07-05X
dateEstablished*:	2007-01-01X
recordAuthorizer*:	sjnX
recordMaintainer*:	lktX
recordOriginator*:	lktX
Type:	Concept X
Coordinate terms:	Fabry Disease \| Gangliosidoses \| Gaucher Disease \| Leukodystrophy, Globoid Cell \| Niemann-Pick Diseases \| Sea-Blue Histiocyte Syndrome X
URI:	X
Labels and equivalent concepts:	Sulfatidoosi (fi) X
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