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).

Also Known As:

Syndrome, Maroteaux-Lamy; ARSB Deficiency; Arylsulfatase B Deficiency; Mucopolysaccharidosis 6; Mucopolysaccharidosis Type 6; Mucopolysaccharidosis Type VI; N-Acetylgalactosamine-4-Sulfatase Deficiency; ARSB Deficiencies; Arylsulfatase B Deficiencies; 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; N-Acetylgalactosamine-4-Sulfatase Deficiencies; Type 6, Mucopolysaccharidosis; Type VI, Mucopolysaccharidosis; Maroteaux-Lamy Syndrome; Polydystrophic Dwarfism

Congenital, Hereditary, and Neonatal Diseases and Abnormalities: 933
- Inborn Genetic Diseases: 11939
  - Inborn Errors Metabolism: 1162
    - Lysosomal Storage Diseases: 2132
      - Mucopolysaccharidoses: 1610
        Mucopolysaccharidosis VI: 321
    - Inborn Errors Carbohydrate Metabolism
      - Mucopolysaccharidoses: 1610
        Mucopolysaccharidosis VI: 321
Skin and Connective Tissue Diseases
- Connective Tissue Diseases: 3269
  - Mucinoses: 170
    - Mucopolysaccharidoses: 1610
      - Mucopolysaccharidosis VI: 321
Nutritional and Metabolic Diseases: 15
- Metabolic Diseases: 10142
  - Inborn Errors Metabolism: 1162
    - Lysosomal Storage Diseases: 2132
      - Mucopolysaccharidoses: 1610
        Mucopolysaccharidosis VI: 321
    - Inborn Errors Carbohydrate Metabolism
      - Mucopolysaccharidoses: 1610
        Mucopolysaccharidosis VI: 321

Danniel da Silva Selected Research

Danniel da Silva Research Topics

Disease

Drug/Important Bio-Agent (IBA)