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PedAM

Pediatric Disease Annotations & Medicines



   peptic esophagitis
  

Disease ID 1069
Disease peptic esophagitis
Definition
INFLAMMATION of the ESOPHAGUS that is caused by the reflux of GASTRIC JUICE with contents of the STOMACH and DUODENUM.
Synonym
esophagitides, peptic
esophagitides, reflux
esophagitis peptic
esophagitis reflux
esophagitis refluxing
esophagitis, peptic
esophagitis, peptic [disease/finding]
esophagitis, reflux
peptic esophagitides
peptic oesophagitis
peptic reflux disease
peptic reflux disease (disorder)
peptic reflux esophagitis
peptic reflux oesophagitis
reflux esophagitides
reflux esophagitis
reflux oesophagitis
DOID
UMLS
C0014869
MeSH
SNOMED-CT
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:1)
C0019291  |  hiatus hernia  |  1
Curated Gene
Entrez_id | Symbol | Resource(Total Genes:1)
CXCL8  |  3576  |  CTD_human
Inferring Gene
Entrez_id | Symbol | Resource(Total Genes:1)
1557  |  CYP2C19  |  infer
Text Mined Gene
Entrez_id | Symbol | Score | Resource(Total Genes:72)
55359  |  STYK1  |  DISEASES
6343  |  SCT  |  DISEASES
9812  |  KIAA0141  |  DISEASES
479  |  ATP12A  |  DISEASES
2862  |  MLNR  |  DISEASES
27121  |  DKK4  |  DISEASES
1777  |  DNASE2  |  DISEASES
4353  |  MPO  |  DISEASES
6347  |  CCL2  |  DISEASES
56920  |  SEMA3G  |  DISEASES
654231  |  OCM  |  DISEASES
2952  |  GSTT1  |  DISEASES
4951  |  OCM2  |  DISEASES
26122  |  EPC2  |  DISEASES
3569  |  IL6  |  DISEASES
490  |  ATP2B1  |  DISEASES
2294  |  FOXF1  |  DISEASES
495  |  ATP4A  |  DISEASES
3553  |  IL1B  |  DISEASES
3938  |  LCT  |  DISEASES
53831  |  GPR84  |  DISEASES
7157  |  TP53  |  DISEASES
7462  |  LAT2  |  DISEASES
7032  |  TFF2  |  DISEASES
4056  |  LTC4S  |  DISEASES
6352  |  CCL5  |  DISEASES
27306  |  HPGDS  |  DISEASES
3577  |  CXCR1  |  DISEASES
213  |  ALB  |  DISEASES
5066  |  PAM  |  DISEASES
23627  |  PRND  |  DISEASES
1857  |  DVL3  |  DISEASES
132243  |  H1FOO  |  DISEASES
4843  |  NOS2  |  DISEASES
3855  |  KRT7  |  DISEASES
2520  |  GAST  |  DISEASES
6546  |  SLC8A1  |  DISEASES
2689  |  GH2  |  DISEASES
55256  |  ADI1  |  DISEASES
23562  |  CLDN14  |  DISEASES
54681  |  P4HTM  |  DISEASES
84639  |  IL1F10  |  DISEASES
1364  |  CLDN4  |  DISEASES
100506658  |  OCLN  |  DISEASES
4638  |  MYLK  |  DISEASES
3360  |  HTR4  |  DISEASES
5743  |  PTGS2  |  DISEASES
6279  |  S100A8  |  DISEASES
1557  |  CYP2C19  |  DISEASES
5225  |  PGC  |  DISEASES
3274  |  HRH2  |  DISEASES
795  |  S100G  |  DISEASES
1045  |  CDX2  |  DISEASES
402682  |  UFSP1  |  DISEASES
79400  |  NOX5  |  DISEASES
1365  |  CLDN3  |  DISEASES
4650  |  MYO9B  |  DISEASES
594857  |  NPS  |  DISEASES
2950  |  GSTP1  |  DISEASES
4295  |  MLN  |  DISEASES
7124  |  TNF  |  DISEASES
7866  |  IFRD2  |  DISEASES
389125  |  MUSTN1  |  DISEASES
4583  |  MUC2  |  DISEASES
338376  |  IFNE  |  DISEASES
149466  |  C1orf210  |  DISEASES
4008  |  LMO7  |  DISEASES
4586  |  MUC5AC  |  DISEASES
4850  |  CNOT4  |  DISEASES
11245  |  GPR176  |  DISEASES
51741  |  WWOX  |  DISEASES
102723508  |  KANTR  |  DISEASES
Locus(Waiting for update.)
Disease ID 1069
Disease peptic esophagitis
Integrated Phenotype(Waiting for update.)
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:2)
HP:0100790  |  Hernia  |  1
HP:0002036  |  Hiatus hernia  |  1
Disease ID 1069
Disease peptic esophagitis
Manually Symptom(Waiting for update.)
Text Mined Symptom(Waiting for update.)
Manually Genotype(Total Text Mining Genotypes:0)
(Waiting for update.)
All Snps(Total Genotypes:6)
snpId pubmedId geneId geneSymbol diseaseId sourceId sentence score Year geneSymbol_dbSNP CHROMOSOME POS REF ALT
rs1052133183492974968OGG1umls:C0014869BeFreeIn a population-based case-control study, we examined associations of the hOGG1 Ser 326 Cys, XRCC1 Arg 399 Gln, and XPD Lys 751 Gln polymorphisms with risk of esophageal adenocarcinoma, Barrett's esophagus, and reflux esophagitis.0.0002714422008OGG1;CAMK139757089CG
rs1052133183492977515XRCC1umls:C0014869BeFreeIn a population-based case-control study, we examined associations of the hOGG1 Ser 326 Cys, XRCC1 Arg 399 Gln, and XPD Lys 751 Gln polymorphisms with risk of esophageal adenocarcinoma, Barrett's esophagus, and reflux esophagitis.0.0002714422008OGG1;CAMK139757089CG
rs25487183492974968OGG1umls:C0014869BeFreeIn a population-based case-control study, we examined associations of the hOGG1 Ser 326 Cys, XRCC1 Arg 399 Gln, and XPD Lys 751 Gln polymorphisms with risk of esophageal adenocarcinoma, Barrett's esophagus, and reflux esophagitis.0.0002714422008XRCC11943551574TC
rs25487183492977515XRCC1umls:C0014869BeFreeIn a population-based case-control study, we examined associations of the hOGG1 Ser 326 Cys, XRCC1 Arg 399 Gln, and XPD Lys 751 Gln polymorphisms with risk of esophageal adenocarcinoma, Barrett's esophagus, and reflux esophagitis.0.0002714422008XRCC11943551574TC
rs386493716183492974968OGG1umls:C0014869BeFreeIn a population-based case-control study, we examined associations of the hOGG1 Ser 326 Cys, XRCC1 Arg 399 Gln, and XPD Lys 751 Gln polymorphisms with risk of esophageal adenocarcinoma, Barrett's esophagus, and reflux esophagitis.0.0002714422008NANANANANA
rs386493716183492977515XRCC1umls:C0014869BeFreeIn a population-based case-control study, we examined associations of the hOGG1 Ser 326 Cys, XRCC1 Arg 399 Gln, and XPD Lys 751 Gln polymorphisms with risk of esophageal adenocarcinoma, Barrett's esophagus, and reflux esophagitis.0.0002714422008NANANANANA
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:5)
CUI ChemicalName ChemicalID CasRN DiseaseName DiseaseID DirectEvidence PubMedIDs
C0014869cimetidineD00292751481-61-9esophagitis, pepticMESH:D004942therapeutic7427548
C0014869lansoprazoleD064747-esophagitis, pepticMESH:D004942therapeutic10594396
C0014869nizatidineD01656776963-41-2esophagitis, pepticMESH:D004942therapeutic15683433
C0014869omeprazoleD00985373590-58-6esophagitis, pepticMESH:D004942therapeutic11350494
C0014869pantoprazoleC064276102625-70-7esophagitis, pepticMESH:D004942therapeutic7762175
FDA approved drug and dosage information(Total Drugs:0)
(Waiting for update.)
FDA labeling changes(Total Drugs:0)
(Waiting for update.)