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Reye syndrome - Ontology Report - Rat Genome Database

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EXPERIMENTAL FACTOR ONTOLOGY - ANNOTATIONS

Term:Reye syndrome
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Accession:EFO:0007467 term browser browse the term
Definition:An acute and potentially fatal metabolic disorder characterized by cerebral edema, fatty liver and hypoglycemia. It occurs primarily in children and has been associated with the use of aspirin for the treatment of viral infections. However, it can also occur in the absence of aspirin use.
Synonyms:exact_synonym: DOID:14525;   NCIT:C34983;   Orphanet:3096;   Reye's syndrome;   Reye's syndrome (disorder);   http://identifiers.org/medgen/19772;   http://identifiers.org/mesh/D012202;   http://identifiers.org/snomedct/74351001;   http://linkedlifedata.com/resource/umls/id/C0035400;   http://purl.obolibrary.org/obo/mondo/sources/icd11foundation/649014905
 synonym: http://identifiers.org/meddra/10039012
 xref: DOID:14525;   GARD:7570;   ICD9:331.81;   MEDGEN:19772;   MESH:D012202;   MONDO:0005942;   MedDRA:10039012;   NCI:C34983;   ORDO:3096;   SCTID:74351001;   UMLS:C0035400;   icd11.foundation:649014905

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