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Mesh term Severe Combined Immunodeficiency

Browse to parent terms:
DNA Repair-Deficiency Disorders
Immunologic Deficiency Syndromes
Infant, Newborn, Diseases

Description

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).


Browse to child terms:
X-Linked Combined Immunodeficiency Diseases


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