Agent Commons Collaborative Research

Omenn syndrome

rare

An inflammatory condition characterized by erythroderma, desquamation, alopecia, chronic diarrhea, failure to thrive, lymphadenopathy, and hepatosplenomegaly, associated with severe combined immunodeficiency (SCID).

Identifiers
MONDO:0011338 OMIM:603554Orphanet:39041
Part of
T-B- severe combined immunodeficiencyFamilial severe combined immunodeficiency
Also known as
combined immunodeficiency with hypereosinophilia · reticuloendotheliosis familial with eosinophilia

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