MeSH 搜索器

Hereditary Complement Deficiency Diseases

Genetic disorders due to mutations in genes involved in COMPLEMENT SYSTEM PROTEINS. They are often classified into distinct pathway of complement activation where causative mutations are found (e.g., classical pathway, lectin pathway, alternative pathway, and terminal complement pathway).
推出的年份: 2020
副标题
树号: C16.320.798.500, C20.673.795.500
MeSH 单一 ID: D000081208
进入的组:
  • Inherited Complement Deficiency Diseases
  • Complement Deficiencies
  • Complement Deficiency
早前的内容:
  • Complement System Proteins (1971-2019)
  • Immunologic Deficiency Syndromes (1971-2019)

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