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Mucopolysaccharidosis VI
Hierarchy: | ∟ ∟ ∟ ∟ ∟ ∟ Mucopolysaccharidosis VI 5 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Mucopolysaccharidosis VI 5 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Mucopolysaccharidosis VI 5 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Mucopolysaccharidosis VI 5 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Mucopolysaccharidosis VI 5 coordinate concepts∟ ∟ ∟ ∟ ∟ |
Broader terms: | ∟ ∟ ∟ ∟ ∟ ∟ Mucopolysaccharidosis VI ∟ ∟ ∟ ∟ ∟ ∟ Mucopolysaccharidosis VI ∟ ∟ ∟ ∟ ∟ ∟ Mucopolysaccharidosis VI ∟ ∟ ∟ ∟ ∟ ∟ Mucopolysaccharidosis VI ∟ ∟ ∟ ∟ ∟ Mucopolysaccharidosis VI |
Annotation: | do not use /congen & do not coord with INFANT, NEWBORN, DISEASES; DF: MPS VI
X |
History note: | Carbohydrate Metabolism, Inborn Errors (1966-1974) | Chondroitin (1966-1974) | Mucopolysaccharides/metabolism (1966-1974) | Mucopolysaccharidosis (1974)X |
historyNote*: | 92; was MUCOPOLYSACCHARIDOSIS 6 1991; was see under MUCOPOLYSACCHARIDOSIS 1975-90
X |
onlineNote*: | use MUCOPOLYSACCHARIDOSIS VI to search MUCOPOLYSACCHARIDOSIS 6 1975-91
X |
publicMeSHNote*: | 92; was MUCOPOLYSACCHARIDOSIS 6 1991; was see under MUCOPOLYSACCHARIDOSIS 1975-90
X |
Scope note: | Mucopolysaccharidosis with excessive chondroitin sulfate B in urine, characterized by dwarfism and deafness. It is caused by a deficiency of N-acetylgalactosamine-4-sulfatase (arylsulfatase B).
X |
activeMeSHYear*: | 2007X |
dateCreated*: | 1974-12-12X |
dateEstablished*: | 1991-01-01X |
dateRevised*: | 2006-07-05X |
recordAuthorizer*: | sjnX |
recordMaintainer*: | lktX |
recordOriginator*: | NLMX |
Type: | |
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Labels and equivalent concepts: | Mukopolysakkaridoosi VI (fi) XPolydystrophic Dwarfism (en, replaced) Mucopolysaccharidosis 6 (en, replaced) Maroteaux-Lamy Syndrome (en, replaced) Mucopolisacaridosis VI (es) βλεννοπολυσακχαρίδωση VI (el) Mukopolysaccharidose Typ VI (de) mukopolysacharidóza VI (cs) Enanismo Polidistrófico (es, replaced) Síndrome de Maroteaux-Lamy (es, replaced) Polydystropher Zwergwuchs (de, replaced) Maroteaux-Lamy-Krankheit (de, replaced) |
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