Omenn syndrome

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Name:
Omenn syndrome
Description:
Omenn syndrome (OS) is an inflammatory condition characterized by erythroderma, desquamation, alopecia, chronic diarrhea, failure to thrive, lymphadenopathy, and hepatosplenomegaly, associated with severe combined immunodeficiency (SCID; see this term).
ORPHAcode:
39041
Synonyms:
Combined immunodeficiency with hypereosinophilia
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Analyte(s):
Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14