| Descriptor English: | Mucopolysaccharidosis VI | ||||||
| Descriptor Spanish: |
Mucopolisacaridosis VI
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| Descriptor Portuguese: | Mucopolissacaridose VI | ||||||
| Descriptor French: | Mucopolysaccharidose de type VI | ||||||
| Entry term(s): |
ARSB Deficiencies ARSB Deficiency Arylsulfatase B Deficiencies Arylsulfatase B Deficiency Deficiencies, ARSB Deficiencies, Arylsulfatase B Deficiencies, N-Acetylgalactosamine-4-Sulfatase Deficiency, ARSB Deficiency, Arylsulfatase B Deficiency, N-Acetylgalactosamine-4-Sulfatase Dwarfism, Polydystrophic Maroteaux Lamy Syndrome Maroteaux-Lamy Syndrome Mucopolysaccharidosis 6 Mucopolysaccharidosis Type 6 Mucopolysaccharidosis Type VI N-Acetylgalactosamine-4-Sulfatase Deficiencies N-Acetylgalactosamine-4-Sulfatase Deficiency Polydystrophic Dwarfism Syndrome, Maroteaux-Lamy Type 6, Mucopolysaccharidosis Type VI, Mucopolysaccharidosis |
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| Tree number(s): |
C16.320.565.202.715.670 C16.320.565.595.600.670 C17.300.550.575.670 C18.452.648.202.715.670 C18.452.648.595.600.670 |
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| RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D009087 | ||||||
| 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). |
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| Allowable Qualifiers: |
BL blood CF cerebrospinal fluid CI chemically induced CL classification CO complications DG diagnostic imaging DH diet therapy DI diagnosis DT drug therapy EC economics EH ethnology EM embryology EN enzymology EP epidemiology ET etiology GE genetics HI history IM immunology ME metabolism MI microbiology MO mortality NU nursing PA pathology PC prevention & control PP physiopathology PS parasitology PX psychology RH rehabilitation RT radiotherapy SU surgery TH therapy UR urine VE veterinary VI virology |
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| Previous Indexing: |
Carbohydrate Metabolism, Inborn Errors (1966-1974) Chondroitin (1966-1974) Mucopolysaccharides/metabolism (1966-1974) Mucopolysaccharidosis (1974) |
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| Public MeSH Note: | 92; was MUCOPOLYSACCHARIDOSIS 6 1991; was see under MUCOPOLYSACCHARIDOSIS 1975-90 |
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| Online Note: | use MUCOPOLYSACCHARIDOSIS VI to search MUCOPOLYSACCHARIDOSIS 6 1975-91 |
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| History Note: | 92; was MUCOPOLYSACCHARIDOSIS 6 1991; was see under MUCOPOLYSACCHARIDOSIS 1975-90 |
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| Entry Version: | MPS VI |
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| DeCS ID: | 30391 | ||||||
| Unique ID: | D009087 | ||||||
| Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||||
| Date Established: | 1991/01/01 | ||||||
| Date of Entry: | 1974/12/12 | ||||||
| Revision Date: | 2013/07/08 |
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Mucopolysaccharidosis VI
- Preferred
| Concept UI |
M0014176 |
| 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). |
| Preferred term | Mucopolysaccharidosis VI |
| Entry term(s) |
ARSB Deficiencies ARSB Deficiency Arylsulfatase B Deficiencies Arylsulfatase B Deficiency Deficiencies, ARSB Deficiencies, Arylsulfatase B Deficiencies, N-Acetylgalactosamine-4-Sulfatase Deficiency, ARSB Deficiency, Arylsulfatase B Deficiency, N-Acetylgalactosamine-4-Sulfatase Dwarfism, Polydystrophic Maroteaux Lamy Syndrome Maroteaux-Lamy Syndrome Mucopolysaccharidosis 6 Mucopolysaccharidosis Type 6 Mucopolysaccharidosis Type VI N-Acetylgalactosamine-4-Sulfatase Deficiencies N-Acetylgalactosamine-4-Sulfatase Deficiency Polydystrophic Dwarfism Syndrome, Maroteaux-Lamy Type 6, Mucopolysaccharidosis Type VI, Mucopolysaccharidosis |
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