Mucopolysaccharidosis type 6 (Q40079)
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Mucopolysaccharidosis type 6 (MPS VI) is a lysosomal storage disease with progressive multisystem involvement, associated with a deficiency of arylsulfatase B (ASB) leading to the accumulation of dermatan sulfate. The disorder shows a wide spectrum of symptoms from slowly to rapidly progressing forms.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | 5C56.33 |
||
| English | Mucopolysaccharidosis type 6 |
Mucopolysaccharidosis type 6 (MPS VI) is a lysosomal storage disease with progressive multisystem involvement, associated with a deficiency of arylsulfatase B (ASB) leading to the accumulation of dermatan sulfate. The disorder shows a wide spectrum of symptoms from slowly to rapidly progressing forms. |
Statements
CID11:5C56.33
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dki-india-5C56.33
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Concluído
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13 August 2026
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