Severe combined immunodeficiency with hypereosinophilia (Q56061)
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Omenn syndrome (OS) is an inflammatory condition characterised by erythroderma, desquamation, alopecia, chronic diarrhea, failure to thrive, lymphadenopathy, and hepatosplenomegaly, associated with severe combined immunodeficiency (SCID; ).
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1770823271 |
||
| English | Severe combined immunodeficiency with hypereosinophilia |
Omenn syndrome (OS) is an inflammatory condition characterised by erythroderma, desquamation, alopecia, chronic diarrhea, failure to thrive, lymphadenopathy, and hepatosplenomegaly, associated with severe combined immunodeficiency (SCID; ). |
Statements
CID11:ID_1770823271
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dki-india-ID_1770823271
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Concluído
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13 August 2026
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