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... > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Metabolism, Inborn Errors > Carbohydrate Metabolism, Inborn Errors > Mucopolysaccharidoses > Mucopolysaccharidosis VI
... > Nutritional and Metabolic Diseases > Metabolic Diseases > Metabolism, Inborn Errors > Carbohydrate Metabolism, Inborn Errors > Mucopolysaccharidoses > Mucopolysaccharidosis VI
Skin and Connective Tissue Diseases > Connective Tissue Diseases > Mucinoses > Mucopolysaccharidoses > Mucopolysaccharidosis VI
... > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Metabolism, Inborn Errors > Lysosomal Storage Diseases > Mucopolysaccharidoses > Mucopolysaccharidosis VI
... > Nutritional and Metabolic Diseases > Metabolic Diseases > Metabolism, Inborn Errors > Lysosomal Storage Diseases > Mucopolysaccharidoses > Mucopolysaccharidosis VI

Preferred term

Mucopolysaccharidosis VI  

Type

  • mesh:Descriptor

Definition

  • 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).

Broader concept

Entry terms

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

Allowable Qualifier(s)

In other languages

  • Mucopolysaccharidose de type VI

    French

  • Déficit en arylsulfatase B
  • Maladie de Maroteaux-Lamy
  • MPS VI
  • Mucopolysaccharidose de type 6
  • Nanisme polydystrophique de Maroteaux-Lamy
  • Syndrome de Maroteaux-Lamy

URI

http://data.loterre.fr/ark:/67375/JVR-GMCP4SXC-K

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