Idiopathic Hypereosinophilic Syndrome

Preferred Label : Idiopathic Hypereosinophilic Syndrome;

NCIt synonyms : Hyper Eosinophilic Syndrome; iHES;

NCIt related terms : Hypereosinophilic syndrome [HES], unspecified; Idiopathic hypereosinophilic syndrome [HES]; Hypereosinophilic Syndrome;

NCIt definition : A syndrome characterized by persistent eosinophilia, for which no underlying cause can be found, and which is associated with signs of organ involvement and dysfunction. This term has often been applied to cases of chronic eosinophilic leukemia. (WHO, 2001);

ICD-O code : 9964/3;

Codes from synonyms : D72.119; D72.110;

Details

Origin ID

C27038;

UMLS CUI

C0206141;

Automatic exact mappings (from CISMeF team)
- Chronic eosinophilic leukaemia [ICD-11 Extension code]
- Hypereosinophilic syndrome (morphologic abnormality) [SNOMED CT concept]
- eosinophilic disorders [MedlinePlus Topic]
Currated CISMeF NLP mapping
- Hypereosinophilic syndrome [ICD-O code]
- Hypereosinophilic syndrome [PASCAL descriptor]
- Hypereosinophilic syndrome [ICD-11 More detail]
- Hypereosinophilic syndrome [MedDRA Preferred Term]
- Hypereosinophilic syndrome [ORDO Disease]
- Hypereosinophilic syndrome (disorder) [SNOMED CT concept]
- Hypereosinophilic syndrome, idiopathic [OMIM Phenotype]
- Hypereosinophilic syndrome/chronic eosinophilic leukemia (morphologic abnormality) [Inactive SNOMED CT concept]
- Idiopathic hypereosinophilic syndrome (disorder) [SNOMED CT concept]
- hypereosinophilic syndrome [DO Concept]
- hypereosinophilic syndrome [Disease (Nov.)]
- hypereosinophilic syndrome [MeSH Descriptor]
- hypereosinophilic syndrome [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Hypereosinophilic syndrome [ORDO Disease]
- Hypereosinophilic syndrome [ICD-O code]
- Hypereosinophilic syndrome [MedDRA Preferred Term]
- Hypereosinophilic syndrome (disorder) [SNOMED CT concept]
- Hypereosinophilic syndrome (morphologic abnormality) [SNOMED CT concept]
- Hypereosinophilic syndrome, idiopathic [OMIM Phenotype]
- Hypereosinophilic syndrome/chronic eosinophilic leukemia (morphologic abnormality) [Inactive SNOMED CT concept]
- Idiopathic hypereosinophilic syndrome [ORDO Disease]
- Idiopathic hypereosinophilic syndrome (disorder) [SNOMED CT concept]
- Idiopathic hypereosinophilic syndrome (morphologic abnormality) [SNOMED CT concept]
- hypereosinophilic syndrome [MeSH concept]
- hypereosinophilic syndrome [MeSH Descriptor]
- idiopathic hypereosinophilic syndrome [MeSH concept]
associated_with_malfunction_of_gene_product
- Interleukin-5 [NCIt concept]
concept_is_in_subset
- CTRP Disease Terminology [NCIt concept]
- CTRP Terminology [NCIt concept]
- GDC Terminology [NCIt concept]
- GDC Value Terminology [NCIt concept]
- mCode Cancer Disorder Value Set [NCIt concept]
- mCode Primary Cancer Disorder Value Set [NCIt concept]
- mCode Specific Diagnosis of Cancer Value Set [NCIt concept]
- mCode Terminology [NCIt concept]
disease_excludes_finding
- Monoclonal Eosinophils Present [NCIt concept]
disease_has_associated_gene
- IL5 Gene [NCIt concept]
- IL5 wt Allele [NCIt concept]
disease_has_finding
- Eosinophilia [NCIt concept]

Keyword's position in hierarchy(ies) :

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