Severe combined immunodeficiency with hypereosinophilia (Q56061): Difference between revisions
From determinar.ia.br - Determine suas informações
Changed an Item |
Changed an Item |
||
| Property / CURIE | |||
CID11:ID_1770823271 | |||
| Property / CURIE: CID11:ID_1770823271 / rank | |||
Normal rank | |||
Revision as of 03:44, 14 August 2026
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
0 references
