Mucopolysaccharidosis VI
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).
Year introduced: 1992
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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
MeSH Unique ID: D009087
Entry Terms:
- ARSB Deficiency
- ARSB Deficiencies
- Deficiencies, ARSB
- Deficiency, ARSB
- Arylsulfatase B Deficiency
- Arylsulfatase B Deficiencies
- Deficiencies, Arylsulfatase B
- Deficiency, Arylsulfatase B
- Maroteaux-Lamy Syndrome
- Maroteaux Lamy Syndrome
- Syndrome, Maroteaux-Lamy
- N-Acetylgalactosamine-4-Sulfatase Deficiency
- Deficiencies, N-Acetylgalactosamine-4-Sulfatase
- Deficiency, N-Acetylgalactosamine-4-Sulfatase
- N-Acetylgalactosamine-4-Sulfatase Deficiencies
- Polydystrophic Dwarfism
- Dwarfism, Polydystrophic
- Mucopolysaccharidosis Type VI
- Type VI, Mucopolysaccharidosis
- Mucopolysaccharidosis 6
- Mucopolysaccharidosis Type 6
- Type 6, Mucopolysaccharidosis
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