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ONTOLOGY REPORT - ANNOTATIONS


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
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Reye syndrome term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Alb albumin JBrowse link 14 19,176,275 19,191,793 RGD:14694843
G Txnip thioredoxin interacting protein JBrowse link 2 198,683,168 198,686,971 RGD:13592920

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 15489
    syndrome 5228
      Reye syndrome 2
Path 2
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  disease 0
    Developmental Diseases 8822
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 7612
        genetic disease 7095
          inherited metabolic disorder 1887
            lipid metabolism disorder 744
              lipid storage disease 367
                fatty liver disease 268
                  Reye syndrome 2
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.