MeSH 搜索器

Glycogen Storage Disease Type I

An autosomal recessive disease in which gene expression of glucose-6-phosphatase is absent, resulting in hypoglycemia due to lack of glucose production. Accumulation of glycogen in liver and kidney leads to organomegaly, particularly massive hepatomegaly. Increased concentrations of lactic acid and hyperlipidemia appear in the plasma. Clinical gout often appears in early childhood.
推出的年份: 1989
副标题
树号: C16.320.565.202.449.448, C18.452.648.202.449.448
MeSH 单一 ID: D005953
进入的组:
  • Gierke Disease
  • Disease, Gierke
  • Gierke's Disease
  • Disease, Gierke's
  • Gierkes Disease
  • Glucose-6-Phosphatase Deficiency
  • Deficiencies, Glucose-6-Phosphatase
  • Deficiency, Glucose-6-Phosphatase
  • Glucose 6 Phosphatase Deficiency
  • Glucose-6-Phosphatase Deficiencies
  • Glycogen Storage Disease 1 (GSD I)
  • Glycogenosis 1
  • Hepatorenal Glycogen Storage Disease
  • von Gierke Disease
  • Disease, von Gierke
  • von Gierke's Disease
  • Disease, von Gierke's
  • von Gierkes Disease
  • Deficiency, Glucosephosphatase
  • Deficiencies, Glucosephosphatase
  • Glucosephosphatase Deficiencies
  • Glucosephosphatase Deficiency

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