immunodeficiency 18
MONDO:0014278Also known as: CD3-Epsilon deficiency, IMD18, immunodeficiency 18, immunodeficiency 18, SCID variant, immunodeficiency 18, Severe combined immunodeficiency variant
- MONDO:
- MONDO:0014278
- OMIM:
- 615615 ↗
Rare disease44 associated genes
Description
Immunodeficiency-18 is an autosomal recessive primary immunodeficiency characterized by onset in infancy or early childhood of recurrent infections. Immunologic work-up of the IMD18 SCID patients shows a T cell-negative, B cell-positive, natural killer (NK) cell-positive phenotype, whereas T-cell development is not impaired in the mild form of IMD18.
Associated genes
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