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MeSH 搜索器

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).
推出的年份: 1992
副标题
树号: 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 单一 ID: D009087
进入的组:
  • Arylsulfatase B Deficiency
  • Arylsulfatase B Deficiencies
  • Deficiencies, Arylsulfatase B
  • Deficiency, Arylsulfatase B
  • Maroteaux-Lamy Syndrome
  • Maroteaux Lamy Syndrome
  • Syndrome, Maroteaux-Lamy
  • Mucopolysaccharidosis Type VI
  • Type VI, Mucopolysaccharidosis
  • Mucopolysaccharidosis Type 6
  • Type 6, Mucopolysaccharidosis
  • N-Acetylgalactosamine-4-Sulfatase Deficiency
  • Deficiencies, N-Acetylgalactosamine-4-Sulfatase
  • Deficiency, N-Acetylgalactosamine-4-Sulfatase
  • N-Acetylgalactosamine-4-Sulfatase Deficiencies
  • Polydystrophic Dwarfism
  • Dwarfism, Polydystrophic
  • ARSB Deficiency
  • ARSB Deficiencies
  • Deficiencies, ARSB
  • Deficiency, ARSB
  • Mucopolysaccharidosis 6
早前的内容:
  • Carbohydrate Metabolism, Inborn Errors (1966-1974)
  • Chondroitin (1966-1974)
  • Mucopolysaccharides/metabolism (1966-1974)
  • Mucopolysaccharidosis (1974)

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