Severe combined immunodeficiency with hypereosinophilia

Preferred Label : Severe combined immunodeficiency with hypereosinophilia;

ICD-11 definition : 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; ).;

ICD-11 synonym : SCID - [severe combined immunodeficiency] with hypereosinophilia; Omenn syndrome; SCID with hypereosinophilia;

Détails

Origin ID

1770823271;

Currated CISMeF NLP mapping
- Omenn Syndrome [NCIt concept]
- Omenn syndrome [OMIM Phenotype]
- Omenn syndrome [DO Concept]
- Omenn syndrome [MedDRA Preferred Term]
- Omenn syndrome [ORDO Disease]
- Omenn syndrome [PASCAL descriptor]
- Omenn syndrome [Disease (Nov.)]
- Severe combined immunodeficiency with hypereosinophilia (disorder) [SNOMED CT concept]
- omenn syndrome [MeSH concept]

Position du mot-clé dans l'(les) arborescence(s) :

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