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RGD DISEASE ONTOLOGY - ANNOTATIONS

RGD uses the Human Disease Ontology (DO, https://disease-ontology.org/) for disease curation across species. RGD automatically downloads each new release of the ontology on a monthly basis. Some additional terms which are required for RGD's curation purposes but are not currently covered in the official version of DO have been added. As corresponding terms are added to DO, these custom terms are retired and the DO terms substituted in existing annotations and subsequently used for curation.
Term:Reye syndrome
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Accession:DOID:14525 term browser browse the term
Definition:A form of encephalopathy with fatty infiltration of the LIVER, characterized by brain EDEMA and VOMITING that may rapidly progress to SEIZURES; COMA; and DEATH. It is caused by a generalized loss of mitochondrial function leading to disturbances in fatty acid and CARNITINE metabolism.
Synonyms:exact_synonym: Adult Reye Syndrome;   Adult Reye's Syndrome;   Fatty Liver with Encephalopathy;   Reye Johnson Syndrome;   Reye Like Syndrome;   Reye's Like Syndrome;   Reye's Syndrome
 primary_id: MESH:D012202;   RDO:0006486
 xref: GARD:7570;   ICD10CM:G93.7;   ICD9CM:331.81;   NCI:C34983
For additional species annotation, visit the Alliance of Genome Resources.


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Reye syndrome term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Alb albumin treatment IEP RGD PMID:25162205 RGD:14694843 NCBI chr14:17,607,397...17,622,814
Ensembl chr14:17,607,381...17,622,836 		JBrowse link
G Txnip thioredoxin interacting protein ISS MouseDO NCBI chr 2:184,093,079...184,096,882
Ensembl chr 2:184,092,991...184,096,886 		JBrowse link
Term paths to the root
Path 1
Term Annotations click to browse term
  disease 18032
    syndrome 9456
      Reye syndrome 2
Path 2
Term Annotations click to browse term
  disease 18032
    Developmental Disease 12742
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 11402
        genetic disease 10994
          inherited metabolic disorder 4645
            lipid metabolism disorder 1146
              lipid storage disease 643
                fatty liver disease 308
                  Reye syndrome 2
paths to the root