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Up to: Familial severe combined immunodeficiency · T-B- severe combined immunodeficiency

Omenn syndrome

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

4 trials tagged with this condition →

This condition has no sub-types.