MeSH 搜索器

Hereditary Angioedema Types I and II

Forms of hereditary angioedema that occur due to mutations in the gene for COMPLEMENT C1 INHIBITOR PROTEIN. Type I hereditary angioedema is associated with reduced serum levels of complement C1 inhibitor protein. Type II hereditary angioedema is associated with the production of a non-functional complement C1 inhibitor protein.
推出的年份: 2010
副标题
树号: C14.907.079.500.750, C17.800.862.945.066.500.750, C20.543.480.904.066.500.750
MeSH 单一 ID: D056829
进入的组:
  • C1 Esterase Inhibitor, Deficiency Of
  • Hereditary Angioedema Type 1
  • Angioedema, Hereditary, Types I and II
  • Deficiency of C1 Esterase Inhibitor
  • Hereditary Angioedema Type I
  • Angioedema, Hereditary, Type I
  • Hereditary Angioedema Type II
  • Angioedema, Hereditary, Type II
早前的内容:
  • Angioedema (1964-2007)
  • Angioedemas, Hereditary (2007-2009)

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