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PedAM

Pediatric Disease Annotations & Medicines



   esophageal disease
  

Disease ID 1304
Disease esophageal disease
Definition
Pathological processes in the ESOPHAGUS.
Synonym
disease esophagus
disease oesophagus
disease of esophagus
disease of esophagus (disorder)
disease of esophagus, nos
disease of oesophagus
disease, esophageal
diseases disorders esophagus
diseases esophagus
diseases of esophagus
diseases of esophagus nos
diseases of esophagus nos (disorder)
diseases of oesophagus
diseases of oesophagus nos
diseases of oesophagus nos (disorder)
diseases of the esophagus
diseases, esophageal
disorder of esophagus
disorder of esophagus (disorder)
disorder of esophagus, nos
disorder of oesophagus
disorders esophagus
disorders oesophageal
esophageal
esophageal dis
esophageal diseases
esophageal diseases [disease/finding]
esophageal disorder
esophageal disorder nos
esophageal disorders
esophageal dysfunction
esophagus
esophagus disease
esophagus diseases
esophagus disorder
esophagus disorders
esophagus--diseases
oesophageal disease
oesophageal diseases
unspecified disorder of esophagus
DOID
UMLS
C0014852
MeSH
SNOMED-CT
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:3)
C0001175  |  acquired immunodeficiency syndrome  |  1
C0011644  |  scleroderma  |  1
C0014868  |  esophagitis  |  1
Curated Gene
Entrez_id | Symbol | Resource(Total Genes:1)
TRPV1  |  7442  |  CTD_human
Inferring Gene(Waiting for update.)
Text Mined Gene
Entrez_id | Symbol | Score | Resource(Total Genes:294)
100885775  |  BANCR  |  DISEASES
6362  |  CCL18  |  DISEASES
10344  |  CCL26  |  DISEASES
1015  |  CDH17  |  DISEASES
54831  |  BEST2  |  DISEASES
3861  |  KRT14  |  DISEASES
6343  |  SCT  |  DISEASES
27248  |  ERLEC1  |  DISEASES
10081  |  PDCD7  |  DISEASES
8086  |  AAAS  |  DISEASES
6554  |  SLC10A1  |  DISEASES
479  |  ATP12A  |  DISEASES
6422  |  SFRP1  |  DISEASES
27121  |  DKK4  |  DISEASES
1178  |  CLC  |  DISEASES
973  |  CD79A  |  DISEASES
9545  |  RAB3D  |  DISEASES
51200  |  CPA4  |  DISEASES
3199  |  HOXA2  |  DISEASES
3202  |  HOXA5  |  DISEASES
6369  |  CCL24  |  DISEASES
4353  |  MPO  |  DISEASES
8288  |  EPX  |  DISEASES
6871  |  TADA2A  |  DISEASES
1440  |  CSF3  |  DISEASES
5539  |  PPY  |  DISEASES
595  |  CCND1  |  DISEASES
2735  |  GLI1  |  DISEASES
3458  |  IFNG  |  DISEASES
2026  |  ENO2  |  DISEASES
9896  |  FIG4  |  DISEASES
3565  |  IL4  |  DISEASES
3567  |  IL5  |  DISEASES
1044  |  CDX1  |  DISEASES
4057  |  LTF  |  DISEASES
9173  |  IL1RL1  |  DISEASES
6909  |  TBX2  |  DISEASES
847  |  CAT  |  DISEASES
652  |  BMP4  |  DISEASES
8189  |  SYMPK  |  DISEASES
30848  |  CTAG2  |  DISEASES
2952  |  GSTT1  |  DISEASES
3232  |  HOXD3  |  DISEASES
8854  |  ALDH1A2  |  DISEASES
417  |  ART1  |  DISEASES
80714  |  PBX4  |  DISEASES
80762  |  NDFIP1  |  DISEASES
56033  |  BARX1  |  DISEASES
54453  |  RIN2  |  DISEASES
1401  |  CRP  |  DISEASES
9201  |  DCLK1  |  DISEASES
57498  |  KIDINS220  |  DISEASES
1828  |  DSG1  |  DISEASES
26122  |  EPC2  |  DISEASES
3569  |  IL6  |  DISEASES
3557  |  IL1RN  |  DISEASES
27348  |  TOR1B  |  DISEASES
7111  |  TMOD1  |  DISEASES
2615  |  LRRC32  |  DISEASES
9360  |  PPIG  |  DISEASES
999  |  CDH1  |  DISEASES
4173  |  MCM4  |  DISEASES
54947  |  LPCAT2  |  DISEASES
6521  |  SLC4A1  |  DISEASES
2294  |  FOXF1  |  DISEASES
495  |  ATP4A  |  DISEASES
25939  |  SAMHD1  |  DISEASES
27134  |  TJP3  |  DISEASES
5024  |  P2RX3  |  DISEASES
3553  |  IL1B  |  DISEASES
735  |  C9  |  DISEASES
89884  |  LHX4  |  DISEASES
60482  |  SLC5A7  |  DISEASES
3938  |  LCT  |  DISEASES
2247  |  FGF2  |  DISEASES
23530  |  NNT  |  DISEASES
2255  |  FGF10  |  DISEASES
5443  |  POMC  |  DISEASES
55722  |  CEP72  |  DISEASES
4171  |  MCM2  |  DISEASES
1950  |  EGF  |  DISEASES
55749  |  CCAR1  |  DISEASES
23598  |  PATZ1  |  DISEASES
7008  |  TEF  |  DISEASES
2252  |  FGF7  |  DISEASES
2627  |  GATA6  |  DISEASES
7157  |  TP53  |  DISEASES
55520  |  ELAC1  |  DISEASES
2064  |  ERBB2  |  DISEASES
151449  |  GDF7  |  DISEASES
3578  |  IL9  |  DISEASES
1956  |  EGFR  |  DISEASES
7462  |  LAT2  |  DISEASES
4851  |  NOTCH1  |  DISEASES
2206  |  MS4A2  |  DISEASES
5531  |  PPP4C  |  DISEASES
3606  |  IL18  |  DISEASES
5805  |  PTS  |  DISEASES
4613  |  MYCN  |  DISEASES
202559  |  KHDRBS2  |  DISEASES
3081  |  HGD  |  DISEASES
7345  |  UCHL1  |  DISEASES
1562  |  CYP2C18  |  DISEASES
4838  |  NODAL  |  DISEASES
7547  |  ZIC3  |  DISEASES
6750  |  SST  |  DISEASES
3815  |  KIT  |  DISEASES
7032  |  TFF2  |  DISEASES
4056  |  LTC4S  |  DISEASES
6352  |  CCL5  |  DISEASES
246  |  ALOX15  |  DISEASES
9965  |  FGF19  |  DISEASES
10630  |  PDPN  |  DISEASES
92291  |  CAPN13  |  DISEASES
27306  |  HPGDS  |  DISEASES
6707  |  SPRR3  |  DISEASES
3577  |  CXCR1  |  DISEASES
84666  |  RETNLB  |  DISEASES
213  |  ALB  |  DISEASES
1359  |  CPA3  |  DISEASES
2982  |  GUCY1A3  |  DISEASES
3600  |  IL15  |  DISEASES
134510  |  UBLCP1  |  DISEASES
7098  |  TLR3  |  DISEASES
1437  |  CSF2  |  DISEASES
6469  |  SHH  |  DISEASES
6778  |  STAT6  |  DISEASES
1632  |  ECI1  |  DISEASES
6356  |  CCL11  |  DISEASES
6037  |  RNASE3  |  DISEASES
7343  |  UBTF  |  DISEASES
6036  |  RNASE2  |  DISEASES
84079  |  ANKRD27  |  DISEASES
7764  |  ZNF217  |  DISEASES
3596  |  IL13  |  DISEASES
3221  |  HOXC4  |  DISEASES
5066  |  PAM  |  DISEASES
196374  |  KRT78  |  DISEASES
123099  |  DEGS2  |  DISEASES
1501  |  CTNND2  |  DISEASES
4176  |  MCM7  |  DISEASES
3213  |  HOXB3  |  DISEASES
29925  |  GMPPB  |  DISEASES
7015  |  TERT  |  DISEASES
6910  |  TBX5  |  DISEASES
2944  |  GSTM1  |  DISEASES
3952  |  LEP  |  DISEASES
8636  |  SSNA1  |  DISEASES
29926  |  GMPPA  |  DISEASES
3170  |  FOXA2  |  DISEASES
2997  |  GYS1  |  DISEASES
27086  |  FOXP1  |  DISEASES
132243  |  H1FOO  |  DISEASES
9370  |  ADIPOQ  |  DISEASES
414325  |  DEFB103A  |  DISEASES
27181  |  SIGLEC8  |  DISEASES
6863  |  TAC1  |  DISEASES
170572  |  HTR3C  |  DISEASES
6657  |  SOX2  |  DISEASES
55894  |  DEFB103B  |  DISEASES
3200  |  HOXA3  |  DISEASES
84875  |  PARP10  |  DISEASES
222256  |  CDHR3  |  DISEASES
79782  |  LRRC31  |  DISEASES
9241  |  NOG  |  DISEASES
3855  |  KRT7  |  DISEASES
1670  |  DEFA5  |  DISEASES
28955  |  DEXI  |  DISEASES
115908  |  CTHRC1  |  DISEASES
2520  |  GAST  |  DISEASES
83482  |  SCRT1  |  DISEASES
6899  |  TBX1  |  DISEASES
64782  |  AEN  |  DISEASES
11251  |  PTGDR2  |  DISEASES
2689  |  GH2  |  DISEASES
4158  |  MC2R  |  DISEASES
503841  |  DEFB106B  |  DISEASES
51738  |  GHRL  |  DISEASES
245909  |  DEFB106A  |  DISEASES
60684  |  TRAPPC11  |  DISEASES
147645  |  VSIG10L  |  DISEASES
885  |  CCK  |  DISEASES
9075  |  CLDN2  |  DISEASES
1058  |  CENPA  |  DISEASES
4842  |  NOS1  |  DISEASES
2246  |  FGF1  |  DISEASES
23583  |  SMUG1  |  DISEASES
60437  |  CDH26  |  DISEASES
51008  |  ASCC1  |  DISEASES
85480  |  TSLP  |  DISEASES
341947  |  COX8C  |  DISEASES
54681  |  P4HTM  |  DISEASES
4089  |  SMAD4  |  DISEASES
2272  |  FHIT  |  DISEASES
1364  |  CLDN4  |  DISEASES
864  |  RUNX3  |  DISEASES
1499  |  CTNNB1  |  DISEASES
23373  |  CRTC1  |  DISEASES
100506658  |  OCLN  |  DISEASES
9815  |  GIT2  |  DISEASES
51155  |  HN1  |  DISEASES
5733  |  PTGER3  |  DISEASES
4638  |  MYLK  |  DISEASES
3360  |  HTR4  |  DISEASES
64779  |  MTHFSD  |  DISEASES
7150  |  TOP1  |  DISEASES
2736  |  GLI2  |  DISEASES
2882  |  GPX7  |  DISEASES
57611  |  ISLR2  |  DISEASES
128153  |  SPATA17  |  DISEASES
6648  |  SOD2  |  DISEASES
7432  |  VIP  |  DISEASES
5743  |  PTGS2  |  DISEASES
4720  |  NDUFS2  |  DISEASES
912  |  CD1D  |  DISEASES
6279  |  S100A8  |  DISEASES
2312  |  FLG  |  DISEASES
4354  |  MPP1  |  DISEASES
10768  |  AHCYL1  |  DISEASES
6658  |  SOX3  |  DISEASES
959  |  CD40LG  |  DISEASES
1557  |  CYP2C19  |  DISEASES
9334  |  B4GALT5  |  DISEASES
8022  |  LHX3  |  DISEASES
7422  |  VEGFA  |  DISEASES
1288  |  COL4A6  |  DISEASES
5225  |  PGC  |  DISEASES
1025  |  CDK9  |  DISEASES
149076  |  ZNF362  |  DISEASES
10783  |  NEK6  |  DISEASES
549  |  AUH  |  DISEASES
3055  |  HCK  |  DISEASES
5394  |  EXOSC10  |  DISEASES
3274  |  HRH2  |  DISEASES
4609  |  MYC  |  DISEASES
6303  |  SAT1  |  DISEASES
5393  |  EXOSC9  |  DISEASES
10631  |  POSTN  |  DISEASES
1059  |  CENPB  |  DISEASES
5983  |  RFC3  |  DISEASES
1045  |  CDX2  |  DISEASES
9189  |  ZBED1  |  DISEASES
438  |  ASMT  |  DISEASES
90865  |  IL33  |  DISEASES
64109  |  CRLF2  |  DISEASES
10771  |  ZMYND11  |  DISEASES
23600  |  AMACR  |  DISEASES
9037  |  SEMA5A  |  DISEASES
402682  |  UFSP1  |  DISEASES
79400  |  NOX5  |  DISEASES
83942  |  TSSK1B  |  DISEASES
5650  |  KLK7  |  DISEASES
3239  |  HOXD13  |  DISEASES
974  |  CD79B  |  DISEASES
338699  |  ANKRD42  |  DISEASES
51520  |  LARS  |  DISEASES
1365  |  CLDN3  |  DISEASES
174  |  AFP  |  DISEASES
2737  |  GLI3  |  DISEASES
133746  |  JMY  |  DISEASES
594857  |  NPS  |  DISEASES
2950  |  GSTP1  |  DISEASES
7442  |  TRPV1  |  DISEASES
440854  |  CAPN14  |  DISEASES
2641  |  GCG  |  DISEASES
4295  |  MLN  |  DISEASES
55636  |  CHD7  |  DISEASES
9343  |  EFTUD2  |  DISEASES
199800  |  ADM5  |  DISEASES
1029  |  CDKN2A  |  DISEASES
8909  |  ENDOU  |  DISEASES
7124  |  TNF  |  DISEASES
7866  |  IFRD2  |  DISEASES
10499  |  NCOA2  |  DISEASES
7072  |  TIA1  |  DISEASES
5334  |  PLCL1  |  DISEASES
4588  |  MUC6  |  DISEASES
54900  |  LAX1  |  DISEASES
2263  |  FGFR2  |  DISEASES
389125  |  MUSTN1  |  DISEASES
3586  |  IL10  |  DISEASES
4583  |  MUC2  |  DISEASES
54625  |  PARP14  |  DISEASES
6949  |  TCOF1  |  DISEASES
134430  |  WDR36  |  DISEASES
4008  |  LMO7  |  DISEASES
4586  |  MUC5AC  |  DISEASES
83481  |  EPPK1  |  DISEASES
1232  |  CCR3  |  DISEASES
5125  |  PCSK5  |  DISEASES
51741  |  WWOX  |  DISEASES
6625  |  SNRNP70  |  DISEASES
102723508  |  KANTR  |  DISEASES
83655  |  LINC00208  |  DISEASES
Locus(Waiting for update.)
Disease ID 1304
Disease esophageal disease
Integrated Phenotype(Waiting for update.)
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:4)
Disease ID 1304
Disease esophageal disease
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:1)
snpId pubmedId geneId geneSymbol diseaseId sourceId sentence score Year geneSymbol_dbSNP CHROMOSOME POS REF ALT
rs917997226644708807IL18RAPumls:C0014852BeFreeThe CC genotype at IL-18RAP locus rs917997 was associated with a protective effect against esophageal disease (P = 6 × 10(-4), odds ratio (OR) = 0.59, and 95% confidence interval (CI) 0.43-0.80 for BE; and P = 2 × 10(-6), OR = 0.46, and 95% CI 0.34-0.64 for EAC).0.0002714422012NA2102454108TC
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
C0014852capsaicinD002211404-86-4esophageal diseasesMESH:D004935marker/mechanism19566590
C0014852cisplatinD00294515663-27-1esophageal diseasesMESH:D004935marker/mechanism1508652
C0014852diclofenacD00400815307-86-5esophageal diseasesMESH:D004935marker/mechanism2022160
C0014852lansoprazoleD064747-esophageal diseasesMESH:D004935therapeutic16440542
C0014852theophyllineD01380658-55-9esophageal diseasesMESH:D004935therapeutic12498299
FDA approved drug and dosage information(Total Drugs:0)
(Waiting for update.)
FDA labeling changes(Total Drugs:0)
(Waiting for update.)