ONKI3 | Medical Subject Headings

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Mucopolysaccharidosis II

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Hierarchy:	Medical Subject Headings (MeSH) ∟ Behavior and Behavior Mechanisms ∟ Neurobehavioral Manifestations ∟ Mental Retardation ∟ Mental Retardation, X-Linked ∟ Mucopolysaccharidosis II 13 coordinate concepts ∟ Mucopolysaccharidosis I \| ∟ Mucopolysaccharidosis III \| ∟ Mucopolysaccharidosis IV \| ∟ Mucopolysaccharidosis VI \| ∟ Mucopolysaccharidosis VII \| ∟ Adrenoleukodystrophy \| ∟ Coffin-Lowry Syndrome \| ∟ Fragile X Syndrome \| ∟ Glycogen Storage Disease Type IIb \| ∟ Lesch-Nyhan Syndrome \| ∟ Menkes Kinky Hair Syndrome \| ∟ Pyruvate Dehydrogenase Complex Deficiency Disease \| ∟ Rett Syndrome Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Genetic Diseases, X-Linked ∟ Mental Retardation, X-Linked ∟ Mucopolysaccharidosis II 13 coordinate concepts ∟ Mucopolysaccharidosis I \| ∟ Mucopolysaccharidosis III \| ∟ Mucopolysaccharidosis IV \| ∟ Mucopolysaccharidosis VI \| ∟ Mucopolysaccharidosis VII \| ∟ Adrenoleukodystrophy \| ∟ Coffin-Lowry Syndrome \| ∟ Fragile X Syndrome \| ∟ Glycogen Storage Disease Type IIb \| ∟ Lesch-Nyhan Syndrome \| ∟ Menkes Kinky Hair Syndrome \| ∟ Pyruvate Dehydrogenase Complex Deficiency Disease \| ∟ Rett Syndrome Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Heredodegenerative Disorders, Nervous System ∟ Mental Retardation, X-Linked ∟ Mucopolysaccharidosis II 13 coordinate concepts ∟ Mucopolysaccharidosis I \| ∟ Mucopolysaccharidosis III \| ∟ Mucopolysaccharidosis IV \| ∟ Mucopolysaccharidosis VI \| ∟ Mucopolysaccharidosis VII \| ∟ Adrenoleukodystrophy \| ∟ Coffin-Lowry Syndrome \| ∟ Fragile X Syndrome \| ∟ Glycogen Storage Disease Type IIb \| ∟ Lesch-Nyhan Syndrome \| ∟ Menkes Kinky Hair Syndrome \| ∟ Pyruvate Dehydrogenase Complex Deficiency Disease \| ∟ Rett Syndrome Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Metabolism, Inborn Errors ∟ Carbohydrate Metabolism, Inborn Errors ∟ Mucopolysaccharidoses ∟ Mucopolysaccharidosis II 13 coordinate concepts ∟ Mucopolysaccharidosis I \| ∟ Mucopolysaccharidosis III \| ∟ Mucopolysaccharidosis IV \| ∟ Mucopolysaccharidosis VI \| ∟ Mucopolysaccharidosis VII \| ∟ Adrenoleukodystrophy \| ∟ Coffin-Lowry Syndrome \| ∟ Fragile X Syndrome \| ∟ Glycogen Storage Disease Type IIb \| ∟ Lesch-Nyhan Syndrome \| ∟ Menkes Kinky Hair Syndrome \| ∟ Pyruvate Dehydrogenase Complex Deficiency Disease \| ∟ Rett Syndrome Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Metabolism, Inborn Errors ∟ Lysosomal Storage Diseases ∟ Mucopolysaccharidoses ∟ Mucopolysaccharidosis II 13 coordinate concepts ∟ Mucopolysaccharidosis I \| ∟ Mucopolysaccharidosis III \| ∟ Mucopolysaccharidosis IV \| ∟ Mucopolysaccharidosis VI \| ∟ Mucopolysaccharidosis VII \| ∟ Adrenoleukodystrophy \| ∟ Coffin-Lowry Syndrome \| ∟ Fragile X Syndrome \| ∟ Glycogen Storage Disease Type IIb \| ∟ Lesch-Nyhan Syndrome \| ∟ Menkes Kinky Hair Syndrome \| ∟ Pyruvate Dehydrogenase Complex Deficiency Disease \| ∟ Rett Syndrome Medical Subject Headings (MeSH) ∟ Mental Disorders ∟ Mental Disorders Diagnosed in Childhood ∟ Mental Retardation ∟ Mental Retardation, X-Linked ∟ Mucopolysaccharidosis II 13 coordinate concepts ∟ Mucopolysaccharidosis I \| ∟ Mucopolysaccharidosis III \| ∟ Mucopolysaccharidosis IV \| ∟ Mucopolysaccharidosis VI \| ∟ Mucopolysaccharidosis VII \| ∟ Adrenoleukodystrophy \| ∟ Coffin-Lowry Syndrome \| ∟ Fragile X Syndrome \| ∟ Glycogen Storage Disease Type IIb \| ∟ Lesch-Nyhan Syndrome \| ∟ Menkes Kinky Hair Syndrome \| ∟ Pyruvate Dehydrogenase Complex Deficiency Disease \| ∟ Rett Syndrome Medical Subject Headings (MeSH) ∟ Nervous System Diseases ∟ Neurodegenerative Diseases ∟ Heredodegenerative Disorders, Nervous System ∟ Mental Retardation, X-Linked ∟ Mucopolysaccharidosis II 13 coordinate concepts ∟ Mucopolysaccharidosis I \| ∟ Mucopolysaccharidosis III \| ∟ Mucopolysaccharidosis IV \| ∟ Mucopolysaccharidosis VI \| ∟ Mucopolysaccharidosis VII \| ∟ Adrenoleukodystrophy \| ∟ Coffin-Lowry Syndrome \| ∟ Fragile X Syndrome \| ∟ Glycogen Storage Disease Type IIb \| ∟ Lesch-Nyhan Syndrome \| ∟ Menkes Kinky Hair Syndrome \| ∟ Pyruvate Dehydrogenase Complex Deficiency Disease \| ∟ Rett Syndrome Medical Subject Headings (MeSH) ∟ Nervous System Diseases ∟ Neurologic Manifestations ∟ Neurobehavioral Manifestations ∟ Mental Retardation ∟ Mental Retardation, X-Linked ∟ Mucopolysaccharidosis II 13 coordinate concepts ∟ Mucopolysaccharidosis I \| ∟ Mucopolysaccharidosis III \| ∟ Mucopolysaccharidosis IV \| ∟ Mucopolysaccharidosis VI \| ∟ Mucopolysaccharidosis VII \| ∟ Adrenoleukodystrophy \| ∟ Coffin-Lowry Syndrome \| ∟ Fragile X Syndrome \| ∟ Glycogen Storage Disease Type IIb \| ∟ Lesch-Nyhan Syndrome \| ∟ Menkes Kinky Hair Syndrome \| ∟ Pyruvate Dehydrogenase Complex Deficiency Disease \| ∟ Rett Syndrome Medical Subject Headings (MeSH) ∟ Nutritional and Metabolic Diseases ∟ Metabolic Diseases ∟ Metabolism, Inborn Errors ∟ Carbohydrate Metabolism, Inborn Errors ∟ Mucopolysaccharidoses ∟ Mucopolysaccharidosis II 13 coordinate concepts ∟ Mucopolysaccharidosis I \| ∟ Mucopolysaccharidosis III \| ∟ Mucopolysaccharidosis IV \| ∟ Mucopolysaccharidosis VI \| ∟ Mucopolysaccharidosis VII \| ∟ Adrenoleukodystrophy \| ∟ Coffin-Lowry Syndrome \| ∟ Fragile X Syndrome \| ∟ Glycogen Storage Disease Type IIb \| ∟ Lesch-Nyhan Syndrome \| ∟ Menkes Kinky Hair Syndrome \| ∟ Pyruvate Dehydrogenase Complex Deficiency Disease \| ∟ Rett Syndrome Medical Subject Headings (MeSH) ∟ Nutritional and Metabolic Diseases ∟ Metabolic Diseases ∟ Metabolism, Inborn Errors ∟ Lysosomal Storage Diseases ∟ Mucopolysaccharidoses ∟ Mucopolysaccharidosis II 13 coordinate concepts ∟ Mucopolysaccharidosis I \| ∟ Mucopolysaccharidosis III \| ∟ Mucopolysaccharidosis IV \| ∟ Mucopolysaccharidosis VI \| ∟ Mucopolysaccharidosis VII \| ∟ Adrenoleukodystrophy \| ∟ Coffin-Lowry Syndrome \| ∟ Fragile X Syndrome \| ∟ Glycogen Storage Disease Type IIb \| ∟ Lesch-Nyhan Syndrome \| ∟ Menkes Kinky Hair Syndrome \| ∟ Pyruvate Dehydrogenase Complex Deficiency Disease \| ∟ Rett Syndrome Medical Subject Headings (MeSH) ∟ Pathological Conditions, Signs and Symptoms ∟ Signs and Symptoms ∟ Neurologic Manifestations ∟ Neurobehavioral Manifestations ∟ Mental Retardation ∟ Mental Retardation, X-Linked ∟ Mucopolysaccharidosis II 13 coordinate concepts ∟ Mucopolysaccharidosis I \| ∟ Mucopolysaccharidosis III \| ∟ Mucopolysaccharidosis IV \| ∟ Mucopolysaccharidosis VI \| ∟ Mucopolysaccharidosis VII \| ∟ Adrenoleukodystrophy \| ∟ Coffin-Lowry Syndrome \| ∟ Fragile X Syndrome \| ∟ Glycogen Storage Disease Type IIb \| ∟ Lesch-Nyhan Syndrome \| ∟ Menkes Kinky Hair Syndrome \| ∟ Pyruvate Dehydrogenase Complex Deficiency Disease \| ∟ Rett Syndrome Medical Subject Headings (MeSH) ∟ Skin and Connective Tissue Diseases ∟ Connective Tissue Diseases ∟ Mucinoses ∟ Mucopolysaccharidoses ∟ Mucopolysaccharidosis II 13 coordinate concepts ∟ Mucopolysaccharidosis I \| ∟ Mucopolysaccharidosis III \| ∟ Mucopolysaccharidosis IV \| ∟ Mucopolysaccharidosis VI \| ∟ Mucopolysaccharidosis VII \| ∟ Adrenoleukodystrophy \| ∟ Coffin-Lowry Syndrome \| ∟ Fragile X Syndrome \| ∟ Glycogen Storage Disease Type IIb \| ∟ Lesch-Nyhan Syndrome \| ∟ Menkes Kinky Hair Syndrome \| ∟ Pyruvate Dehydrogenase Complex Deficiency Disease \| ∟ Rett Syndrome X
Broader terms:	Medical Subject Headings (MeSH) ∟ Behavior and Behavior Mechanisms ∟ Neurobehavioral Manifestations ∟ Mental Retardation ∟ Mental Retardation, X-Linked ∟ Mucopolysaccharidosis II Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Genetic Diseases, X-Linked ∟ Mental Retardation, X-Linked ∟ Mucopolysaccharidosis II Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Heredodegenerative Disorders, Nervous System ∟ Mental Retardation, X-Linked ∟ Mucopolysaccharidosis II Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Metabolism, Inborn Errors ∟ Carbohydrate Metabolism, Inborn Errors ∟ Mucopolysaccharidoses ∟ Mucopolysaccharidosis II Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Metabolism, Inborn Errors ∟ Lysosomal Storage Diseases ∟ Mucopolysaccharidoses ∟ Mucopolysaccharidosis II Medical Subject Headings (MeSH) ∟ Mental Disorders ∟ Mental Disorders Diagnosed in Childhood ∟ Mental Retardation ∟ Mental Retardation, X-Linked ∟ Mucopolysaccharidosis II Medical Subject Headings (MeSH) ∟ Nervous System Diseases ∟ Neurodegenerative Diseases ∟ Heredodegenerative Disorders, Nervous System ∟ Mental Retardation, X-Linked ∟ Mucopolysaccharidosis II Medical Subject Headings (MeSH) ∟ Nervous System Diseases ∟ Neurologic Manifestations ∟ Neurobehavioral Manifestations ∟ Mental Retardation ∟ Mental Retardation, X-Linked ∟ Mucopolysaccharidosis II Medical Subject Headings (MeSH) ∟ Nutritional and Metabolic Diseases ∟ Metabolic Diseases ∟ Metabolism, Inborn Errors ∟ Carbohydrate Metabolism, Inborn Errors ∟ Mucopolysaccharidoses ∟ Mucopolysaccharidosis II Medical Subject Headings (MeSH) ∟ Nutritional and Metabolic Diseases ∟ Metabolic Diseases ∟ Metabolism, Inborn Errors ∟ Lysosomal Storage Diseases ∟ Mucopolysaccharidoses ∟ Mucopolysaccharidosis II Medical Subject Headings (MeSH) ∟ Pathological Conditions, Signs and Symptoms ∟ Signs and Symptoms ∟ Neurologic Manifestations ∟ Neurobehavioral Manifestations ∟ Mental Retardation ∟ Mental Retardation, X-Linked ∟ Mucopolysaccharidosis II Medical Subject Headings (MeSH) ∟ Skin and Connective Tissue Diseases ∟ Connective Tissue Diseases ∟ Mucinoses ∟ Mucopolysaccharidoses ∟ Mucopolysaccharidosis II Mental Retardation, X-Linked > Mental Retardation > Neurobehavioral Manifestations > Behavior and Behavior Mechanisms > Medical Subject Headings (MeSH) Mental Retardation, X-Linked > Genetic Diseases, X-Linked > Genetic Diseases, Inborn > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Medical Subject Headings (MeSH) Mental Retardation, X-Linked > Heredodegenerative Disorders, Nervous System > Genetic Diseases, Inborn > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Medical Subject Headings (MeSH) 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) Mental Retardation, X-Linked > Mental Retardation > Mental Disorders Diagnosed in Childhood > Mental Disorders > Medical Subject Headings (MeSH) Mental Retardation, X-Linked > Heredodegenerative Disorders, Nervous System > Neurodegenerative Diseases > Nervous System Diseases > Medical Subject Headings (MeSH) Mental Retardation, X-Linked > Mental Retardation > Neurobehavioral Manifestations > Neurologic Manifestations > Nervous System Diseases > 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) Mental Retardation, X-Linked > Mental Retardation > Neurobehavioral Manifestations > Neurologic Manifestations > Signs and Symptoms > Pathological Conditions, Signs and Symptoms > Medical Subject Headings (MeSH) Mucopolysaccharidoses > Mucinoses > Connective Tissue Diseases > Skin and Connective Tissue Diseases > Medical Subject Headings (MeSH) X
Annotation:	DF: MPS II X
History note:	Mucopolysaccharidosis I (1966-1991)X
historyNote*:	92; MUCOPOLYSACCHARIDOSIS 2 and HUNTER'S SYNDROME were see LIPOCHONDRODYSTROPHY 1976-91 X
onlineNote*:	use MUCOPOLYSACCHARIDOSIS II to search MUCOPOLYSACCHARIDOSIS 2 & HUNTER'S SYNDROME 1976-91 X
publicMeSHNote*:	92; MUCOPOLYSACCHARIDOSIS 2 and HUNTER'S SYNDROME were see LIPOCHONDRODYSTROPHY 1976-91 X
Scope note:	Systemic lysosomal storage disease marked by progressive physical deterioration and caused by a deficiency of L-sulfoiduronate sulfatase. This disease differs from MUCOPOLYSACCHARIDOSIS I by slower progression, lack of corneal clouding, and X-linked rather than autosomal recessive inheritance. The mild form produces near-normal intelligence and life span. The severe form usually causes death by age 15. X
activeMeSHYear*:	2007X
dateCreated*:	1991-06-21X
dateEstablished*:	1992-01-01X
dateRevised*:	2006-07-05X
recordAuthorizer*:	sjnX
recordMaintainer*:	lktX
recordOriginator*:	AGSX
Related term:	Mucopolysaccharidosis I X
Type:	Concept X
Coordinate terms:	Mucopolysaccharidosis I \| Mucopolysaccharidosis III \| Mucopolysaccharidosis IV \| Mucopolysaccharidosis VI \| Mucopolysaccharidosis VII \| Adrenoleukodystrophy \| Coffin-Lowry Syndrome \| Fragile X Syndrome \| Glycogen Storage Disease Type IIb \| Lesch-Nyhan Syndrome \| Menkes Kinky Hair Syndrome \| Pyruvate Dehydrogenase Complex Deficiency Disease \| Rett Syndrome X
URI:	X
Labels and equivalent concepts:	Mukopolysakkaridoosi II (fi) Hunterin syndrooma (fi, replaced) Hunterin oireyhtymä (fi, replaced) Mukopolysackaridos II (sv) Hunters syndrom (sv, replaced) MPS II (sv, replaced) Hunter Syndrome Gargoylism (en, replaced) Hunter's Syndrome (en, replaced) Mucopolysaccharidosis 2 (en, replaced) Gargoylism, Hunter Syndrome (en, replaced) Mucopolysaccharidosis II (la-FI, replaced) X
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