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immunodeficiency 18

MONDO:0014278

Also known as: CD3-Epsilon deficiency, IMD18, immunodeficiency 18, immunodeficiency 18, SCID variant, immunodeficiency 18, Severe combined immunodeficiency variant

MONDO:
MONDO:0014278
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

+34 more genes — install the extension to see the full list inline on any page.

External references

Sources: MONDO (CC BY 4.0), Open Targets (CC0), Orphanet (CC BY 4.0).

Not for sole clinical decision-making. Always verify against primary sources.