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Pediatric Disease Annotations & Medicines



   reye syndrome
  

Disease ID 445
Disease reye syndrome
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.
Synonym
fatty liver with encephalopathy
reye 's syndrome
reye johnson syndrome
reye syndrome [disease/finding]
reye's encephalopathy
reye's syndrome
reye's syndrome (disorder)
reye-johnson syndrome
reyes syndrome
reyes syndromes
reyes's syndrome
syndrome reye
syndrome reyes
Orphanet
DOID
ICD10
UMLS
C0035400
MeSH
SNOMED-CT
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:2)
C0878544  |  cardiomyopathy  |  1
C0014070  |  encephalomyelitis  |  1
Curated Gene(Waiting for update.)
Inferring Gene(Waiting for update.)
Text Mined Gene
Entrez_id | Symbol | Score | Resource(Total Genes:78)
5009  |  OTC  |  DISEASES
25776  |  CBY1  |  DISEASES
4967  |  OGDH  |  DISEASES
4790  |  NFKB1  |  DISEASES
4055  |  LTBR  |  DISEASES
4848  |  CNOT2  |  DISEASES
2026  |  ENO2  |  DISEASES
6908  |  TBP  |  DISEASES
33  |  ACADL  |  DISEASES
7276  |  TTR  |  DISEASES
6584  |  SLC22A5  |  DISEASES
5199  |  CFP  |  DISEASES
29108  |  PYCARD  |  DISEASES
3630  |  INS  |  DISEASES
29775  |  CARD10  |  DISEASES
10599  |  SLCO1B1  |  DISEASES
27141  |  CIDEB  |  DISEASES
898  |  CCNE1  |  DISEASES
330  |  BIRC3  |  DISEASES
5775  |  PTPN4  |  DISEASES
89884  |  LHX4  |  DISEASES
6507  |  SLC1A3  |  DISEASES
1374  |  CPT1A  |  DISEASES
5286  |  PIK3C2A  |  DISEASES
8996  |  NOL3  |  DISEASES
6506  |  SLC1A2  |  DISEASES
5903  |  RANBP2  |  DISEASES
23250  |  ATP11A  |  DISEASES
60675  |  PROK2  |  DISEASES
213  |  ALB  |  DISEASES
11067  |  C10orf10  |  DISEASES
375611  |  SLC26A5  |  DISEASES
2147  |  F2  |  DISEASES
3661  |  IRF3  |  DISEASES
1375  |  CPT1B  |  DISEASES
28976  |  ACAD9  |  DISEASES
2  |  A2M  |  DISEASES
1555  |  CYP2B6  |  DISEASES
706  |  TSPO  |  DISEASES
1743  |  DLST  |  DISEASES
3988  |  LIPA  |  DISEASES
1576  |  CYP3A4  |  DISEASES
3266  |  ERAS  |  DISEASES
1431  |  CS  |  DISEASES
31  |  ACACA  |  DISEASES
987  |  LRBA  |  DISEASES
1612  |  DAPK1  |  DISEASES
6364  |  CCL20  |  DISEASES
4512  |  MT-CO1  |  DISEASES
4519  |  MT-CYB  |  DISEASES
4508  |  MT-ATP6  |  DISEASES
4513  |  MT-CO2  |  DISEASES
4514  |  MT-CO3  |  DISEASES
23038  |  WDTC1  |  DISEASES
10628  |  TXNIP  |  DISEASES
840  |  CASP7  |  DISEASES
2805  |  GOT1  |  DISEASES
959  |  CD40LG  |  DISEASES
1647  |  GADD45A  |  DISEASES
1376  |  CPT2  |  DISEASES
9968  |  MED12  |  DISEASES
3155  |  HMGCL  |  DISEASES
7295  |  TXN  |  DISEASES
229  |  ALDOB  |  DISEASES
3376  |  IARS  |  DISEASES
3030  |  HADHA  |  DISEASES
6649  |  SOD3  |  DISEASES
4155  |  MBP  |  DISEASES
23410  |  SIRT3  |  DISEASES
3426  |  CFI  |  DISEASES
3033  |  HADH  |  DISEASES
279  |  AMY2A  |  DISEASES
4049  |  LTA  |  DISEASES
34  |  ACADM  |  DISEASES
6256  |  RXRA  |  DISEASES
2110  |  ETFDH  |  DISEASES
4558  |  MT-TF  |  DISEASES
4566  |  MT-TK  |  DISEASES
Locus(Waiting for update.)
Disease ID 445
Disease reye syndrome
Integrated Phenotype(Waiting for update.)
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:4)
HP:0001298  |  Encephalopathy  |  1
HP:0001399  |  Liver failure  |  1
HP:0001638  |  Cardiomyopathy  |  1
HP:0011675  |  Arrhythmias  |  1
Disease ID 445
Disease reye syndrome
Manually Symptom
UMLS  | Name(Total Manually Symptoms:9)
C2364324  |  increased intracranial pressure
C1963198  |  pancreatitis
C1963101  |  encephalopathy
C0151740  |  elevated intracranial pressure
C0042769  |  viral infections
C0037769  |  west syndrome
C0022660  |  acute renal failure
C0005779  |  coagulation defect
C0002063  |  alkalosis
Text Mined Symptom
UMLS | Name | Sentences' Count(Total Symptoms:1)
C0085584  |  encephalopathy  |  1
Manually Genotype(Total Text Mining Genotypes:0)
(Waiting for update.)
All Snps(Total Genotypes:0)
(Waiting for update.)
GWASdb Annotation(Total Genotypes:0)
(Waiting for update.)
GWASdb Snp Trait(Total Genotypes:0)
(Waiting for update.)
Mapped by lexical matching(Total Items:0)
(Waiting for update.)
Mapped by homologous gene(Total Items:0)
(Waiting for update.)
Chemical(Total Drugs:2)
CUI ChemicalName ChemicalID CasRN DiseaseName DiseaseID DirectEvidence PubMedIDs
C0035400diclofenacD00400815307-86-5reye syndromeMESH:D012202marker/mechanism9379106
C0035400valproic acidD01463599-66-1reye syndromeMESH:D012202marker/mechanism6819143
FDA approved drug and dosage information(Total Drugs:0)
(Waiting for update.)
FDA labeling changes(Total Drugs:0)
(Waiting for update.)