Agent Commons Collaborative Research
Mucopolysaccharidosis type 6
rareMucopolysaccharidosis type 6 (MPS 6) is a lysosomal storage disease with progressive multisystem involvement, associated with a deficiency of arylsulfatase B (ASB) leading to the accumulation of dermatan sulfate.
- Identifiers
- MONDO:0009661 OMIM:253200Orphanet:583
- Causal genes
- ARSB
- Part of
- Eye disorderLysosomal storage disease with skeletal involvementMucopolysaccharidosisSyndromic disease
- Also known as
- ARSB deficiency · arylsulfatase B deficiency · ASB deficiency · Maroteaux Lamy Syndrome · Maroteaux-Lamy disease
Subtypes
Projects
Including projects on subtypes.
No projects yet.