Omenn syndrome

MONDO:0011338

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

Also known as: Omenn syndrome, combined immunodeficiency with hypereosinophilia, reticuloendotheliosis familial with eosinophilia, reticuloendotheliosis, familial, with eosinophilia, severe combined immunodeficiency with hypereosinophilia

20 clinical trials for this condition and its sub-types.

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