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hypereosinophilic syndrome

Go to external page http://purl.obolibrary.org/obo/MONDO_0015691

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 ]

Synonyms: hypereosinophilic syndrome hypereosinophilic disorder HES eosinophilic leukocytosis hypereosinophilic disease

This is just here as a test because I lose it

Term information

database cross reference
  • NCIT:C27038 (MONDO:equivalentTo)
  • SCTID:419455006 (MONDO:equivalentTo)
  • EFO:1001467 (MONDO:equivalentTo)
  • MedDRA:10048643 (Orphanet:168956/e)
  • ICD9:288.3 (DOID:999)
  • NANDO:2200805 (https://orcid.org/0000-0003-0011-764X)
  • NANDO:2200806 (https://orcid.org/0000-0003-0011-764X)
  • GARD:2804 (MONDO:GARD)
  • ICDO:9964/3 (NCIT:C27038)
  • MEDGEN:280990 (MONDO:equivalentTo)
  • MESH:D017681 (Orphanet:168956/e)
  • UMLS:C1540912 (MONDO:equivalentTo)
  • Orphanet:168956 (MONDO:equivalentTo)
  • DOID:999 (MONDO:equivalentTo)
Subsets

gard_rare, otar, disease_grouping, rare, nord_rare, ordo_group_of_disorders

abbreviation
HES [ Orphanet:168956 ]

closeMatch

http://identifiers.org/meddra/10048643

exactMatch

http://identifiers.org/snomedct/419455006

http://linkedlifedata.com/resource/umls/id/C1540912

http://purl.obolibrary.org/obo/DOID_999

http://www.orpha.net/ORDO/Orphanet_168956

http://identifiers.org/medgen/280990

http://purl.obolibrary.org/obo/NCIT_C27038

http://identifiers.org/mesh/D017681

excluded from qc check

http://purl.obolibrary.org/obo/mondo/sparql/qc/general/qc-single-child.sparql

has related synonym

eosinophilia

id

MONDO:0015691