Omenn syndrome
MONDO:0011338An 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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Disease
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Hereditary disease
(172)
Immune system disorder
(140)
Immunodeficiency disease
(48)
Severe combined immunodeficiency
(21)
Human disease
(14)
Combined immunodeficiency
(3)
Disease of genetic or genomic mechanism
(2)
Disease by body system or component
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Disease by etiologic mechanism
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