MeSH 搜索器

Mucopolysaccharidosis II

Systemic lysosomal storage disease marked by progressive physical deterioration and caused by a deficiency of L-sulfoiduronate sulfatase. This disease differs from MUCOPOLYSACCHARIDOSIS I by slower progression, lack of corneal clouding, and X-linked rather than autosomal recessive inheritance. The mild form produces near-normal intelligence and life span. The severe form usually causes death by age 15.
推出的年份: 1992
副标题
树号: C10.597.606.360.455.750, C16.320.322.500.750, C16.320.400.525.750, C16.320.565.202.715.645, C16.320.565.595.600.645, C17.300.550.575.645, C18.452.648.202.715.645, C18.452.648.595.600.645
MeSH 单一 ID: D016532
进入的组:
  • Mucopolysaccharidosis 2
  • Hunter Syndrome
  • Syndrome, Hunter
  • Hunter Syndrome Gargoylism
  • Mucopolysaccharidosis Type 2
  • Mucopolysaccharidosis Type II
  • Hunter's Syndrome
  • Hunters Syndrome
  • Syndrome, Hunter's
  • Gargoylism, Hunter Syndrome
  • Sulfoiduronate Sulfatase Deficiency
  • Deficiency, Sulfoiduronate Sulfatase
  • Iduronate 2-Sulfatase Deficiency
  • Deficiency, Iduronate 2-Sulfatase
  • Iduronate 2 Sulfatase Deficiency
  • I2S Deficiency
  • Deficiency, I2S
  • Iduronate Sulfatase Deficiency
  • Deficiency, Iduronate Sulfatase
早前的内容:
  • Mucopolysaccharidosis I (1966-1991)

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