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bn:03519278n
Noun Concept
Categories: Proteoglycan metabolism disorders
EN
mucopolysaccharidosis VI  Maroteaux–Lamy syndrome  deficiency of N-acetylgalactosamine-4-sulfatase  ARSB deficiency  arylsulfatase B deficiency
EN
Maroteaux–Lamy syndrome, or Mucopolysaccharidosis Type VI, is an inherited disease caused by a deficiency in the enzyme arylsulfatase B. Wikipedia
Definitions
Relations
Sources
EN
Maroteaux–Lamy syndrome, or Mucopolysaccharidosis Type VI, is an inherited disease caused by a deficiency in the enzyme arylsulfatase B. Wikipedia
Lysosomal storage disease Wikidata
IS A
rare disease
mucopolysaccharidosis
GENETIC ASSOCIATION
arylsulfatase B
HEALTH SPECIALTY
endocrinology
MODE OF INHERITANCE
dominance
NAMED AFTER
Pierre Maroteaux
Wikipedia
EN
Maroteaux–Lamy syndrome
Wikidata
EN
mucopolysaccharidosis VI
Wikipedia Redirections
EN
Maroteaux-Lamy, Maroteaux-Lamy Syndrome, Maroteaux Lamy disease, MPS6, MPS 6, MPS VI, Mucopolysaccharidosis type 6, Mucopolysaccharidosis Type VI, Mucopolysaccharidosis type VI Maroteaux-Lamy - severe, intermediate, Mucopolysaccharidosis VI, Mucopolysaccharidosis vi, Polydystrophic dwarfism
Wikidata Alias
EN
ARSB deficiency, arylsulfatase B deficiency, ASB deficiency, deficiency of N-acetylgalactosamine-4-sulfatase, Maroteaux-Lamy disease, Maroteaux-Lamy syndrome, Maroteaux - Lamy syndrome, MPS6, Mps 6, MPS VI, MPS VI - Maroteaux-Lamy syndrome, MPSVI, Mucopolysaccharidosis type VI, MUCOPOLYSACCHARIDOSIS TYPE VI; MPS6, mucopolysaccharidosis VI, N-Acetylgalactosamine-4-Sulfatase Deficiency, N-acetylgalactosamine 4-sulfatase deficiency

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