reticuloendotheliosis, familial, with eosinophilia

Preferred Label : reticuloendotheliosis, familial, with eosinophilia;

MeSH synonym : severe combined immunodeficiency with hypereosinophilia;

Details

Origin ID

C538564;

UMLS CUI

C2931884;

CISMeF manual mappings
- Omenn syndrome [ORDO Disease]
- Severe combined immunodeficiency with hypereosinophilia (disorder) [SNOMED CT concept]
Currated CISMeF NLP mapping
- Histiocytic medullary reticulosis (disorder) [SNOMED CT concept]
- Omenn Syndrome [NCIt concept]
- Omenn syndrome [MedDRA Preferred Term]
- Omenn syndrome [PASCAL descriptor]
- Omenn syndrome [OMIM Phenotype]
MeSH term(s) associated for indexing
- eosinophilia [MeSH Descriptor]
- severe combined immunodeficiency [MeSH Descriptor]
Record concept(s)
- Reticuloendotheliosis, familial, with eosinophilia [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Severe combined immunodeficiency with hypereosinophilia (disorder) [SNOMED CT concept]

Keyword's position in hierarchy(ies) :

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