hypereosinophilic syndrome
Hypereosinophilic syndrome (HES) constitutes a rare and heterogeneous group of disorders, defined as persistent and marked blood eosinophilia and/or tissue eosinophilia associated with a wide range of clinical manifestations reflecting eosinophil-induced tissue/organ damage. [ Orphanet:168956 ]
Term info
- Orphanet:168956 (MONDO:equivalentTo)
- ICD9:288.3 (DOID:999)
- MedDRA:10048643 (Orphanet:168956/e)
- NCIT:C27038 (MONDO:equivalentTo)
- SCTID:419455006 (MONDO:equivalentTo)
- UMLS:C1540912 (Orphanet:168956/e)
- GARD:0002804 (MONDO:equivalentTo)
- MESH:D017681 (Orphanet:168956/e)
- DOID:999 (MONDO:equivalentTo)
- ICDO:9964/3 (NCIT:C27038)
- EFO:1001467 (MONDO:equivalentTo)
disease_grouping, ordo_group_of_disorders
http://identifiers.org/meddra/10048643
Hypereosinophilic syndrome (HES) constitutes a rare and heterogeneous group of disorders, defined as persistent and marked blood eosinophilia and/or tissue eosinophilia associated with a wide range of clinical manifestations reflecting eosinophil-induced tissue/organ damage.
http://identifiers.org/snomedct/419455006, http://linkedlifedata.com/resource/umls/id/C1540912, http://purl.obolibrary.org/obo/DOID_999, http://purl.obolibrary.org/obo/NCIT_C27038, http://purl.obolibrary.org/obo/Orphanet_168956, http://identifiers.org/mesh/D017681
hypereosinophilic syndrome, hypereosinophilic disorder, HES, eosinophilic leukocytosis, hypereosinophilic disease
eosinophilia
MONDO:0015691