MeSH 搜索器

Severe Combined Immunodeficiency

Group of rare congenital disorders characterized by impairment of both humoral and cell-mediated immunity, leukopenia, and low or absent antibody levels. It is inherited as an X-linked or autosomal recessive defect. Mutations occurring in many different genes cause human Severe Combined Immunodeficiency (SCID).
推出的年份: 1992
副标题
树号: C16.320.798.750, C16.614.815, C18.452.284.800, C20.673.795.750
MeSH 单一 ID: D016511
进入的组:
  • Combined Immunodeficiencies, Severe
  • Combined Immunodeficiency, Severe
  • Immunodeficiencies, Severe Combined
  • Severe Combined Immunodeficiencies
  • Immunodeficiency Syndrome, Severe Combined
  • Severe Combined Immunodeficiency Syndrome
  • Severe Combined Immunologic Deficiency
  • Immunologic Deficiency, Severe Combined
  • Severe Combined Immune Deficiency
  • Immunodeficiency, Severe Combined
  • Bare Lymphocyte Syndrome
  • Bare Lymphocyte Syndromes
  • Lymphocyte Syndrome, Bare
  • Lymphocyte Syndromes, Bare
  • Syndrome, Bare Lymphocyte
  • Syndromes, Bare Lymphocyte
  • Omenn Syndrome
  • Syndrome, Omenn
  • Reticuloendotheliosis, Familial
  • Familial Reticuloendothelioses
  • Familial Reticuloendotheliosis
  • Reticuloendothelioses, Familial
  • Omenn's Syndrome
  • Omenns Syndrome
  • Syndrome, Omenn's
早前的内容:
  • Immunologic Deficiency Syndromes (1974-1991)

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