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).
Year introduced: 1992
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Subheadings:
Tree Number(s): C16.320.798.750, C16.614.815, C18.452.284.800, C20.673.795.750
MeSH Unique ID: D016511
Entry Terms:
- Combined Immunodeficiencies, Severe
- Combined Immunodeficiency, Severe
- Immunodeficiencies, Severe Combined
- Severe Combined Immunodeficiencies
- Immunodeficiency Syndrome, Severe Combined
- Severe Combined Immunodeficiency Syndrome
- Severe Combined Immune Deficiency
- Immunologic Deficiency, Severe Combined
- Severe Combined Immunologic 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
- Omenn's Syndrome
- Omenns Syndrome
- Syndrome, Omenn's
- Reticuloendotheliosis, Familial
- Familial Reticuloendothelioses
- Familial Reticuloendotheliosis
- Reticuloendothelioses, Familial
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