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MeSH 搜索器

Wolman Disease

The severe infantile form of inherited lysosomal lipid storage diseases due to deficiency of acid lipase (STEROL ESTERASE). It is characterized by the accumulation of neutral lipids, particularly CHOLESTEROL ESTERS in leukocytes, fibroblasts, and hepatocytes. It is also known as Wolman's xanthomatosis and is an allelic variant of CHOLESTEROL ESTER STORAGE DISEASE.
推出的年份: 1989
副标题
树号: C16.320.565.398.641.201.500, C16.320.565.595.201.500, C16.614.947, C18.452.584.563.641.201.500, C18.452.648.398.641.201.500, C18.452.648.595.201.500
MeSH 单一 ID: D015223
进入的组:
  • Disease, Wolman
  • Wolman's Disease
  • Disease, Wolman's
  • Wolmans Disease
  • Familial Xanthomatosis
  • Liposomal Acid Lipase Deficiency, Wolman Type
  • Acid Cholesteryl Ester Hydrolase Deficiency, Wolman Type
  • Acid Lipase Deficiency
  • Xanthomatosis, Familial
  • Familial Xanthomatoses
  • Xanthomatoses, Familial
  • Xanthomatosis, Wolman's
  • Wolman's Xanthomatosis
  • Xanthomatosis, Wolman
  • Xanthomatosis, Wolmans
早前的内容:
  • Cholesterol Esters (1978-1988)
  • Lipase (1966-1988)
  • Lipid Metabolism, Inborn Errors (1966-1988)
  • Lipoidosis (1966-1988)
  • Xanthomatosis (1966-1988)

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