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PedAM

Pediatric Disease Annotations & Medicines



   peptic ulcer disease
  

Disease ID 828
Disease peptic ulcer disease
Definition
Ulcer that occurs in the regions of the GASTROINTESTINAL TRACT which come into contact with GASTRIC JUICE containing PEPSIN and GASTRIC ACID. It occurs when there are defects in the MUCOSA barrier. The common forms of peptic ulcers are associated with HELICOBACTER PYLORI and the consumption of nonsteroidal anti-inflammatory drugs (NSAIDS).
Synonym
site unspecified
gastroduodenal ulcer
gastroduodenal ulcer, nos
gastroduodenal ulcers
peptic ulcer
peptic ulcer (disorder)
peptic ulcer - (pu) site unspecified
peptic ulcer - (pu) site unspecified (disorder)
peptic ulcer [disease/finding]
peptic ulcer disorder
peptic ulcer nos
peptic ulcer nos (disorder)
peptic ulcer nos = pu
peptic ulcer syndrome
peptic ulcer, nos
peptic ulcer, site unspecified
peptic ulceration
peptic ulcers
pu - peptic ulcer
pud - peptic ulcer disease
syndrome peptic ulcer
ulcer gastroduodenal
ulcer of the gastrointestinal tract
ulcer peptic
ulcer syndrome peptic
ulcer, gastroduodenal
ulcer, peptic
ulcers, gastroduodenal
ulcers, peptic
unspecified peptic ulcer
unspecified peptic ulcer (disorder)
unspecified peptic ulcer nos
unspecified peptic ulcer nos (disorder)
DOID
UMLS
C0030920
MeSH
SNOMED-CT
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:36)
C0024623  |  gastric cancer  |  6
C0023890  |  liver cirrhosis  |  3
C0001173  |  gastric outlet obstruction  |  3
C0001418  |  adenocarcinoma  |  2
C0017152  |  gastritis  |  2
C0278701  |  gastric adenocarcinoma  |  2
C0019360  |  herpes zoster  |  1
C0024523  |  malabsorption  |  1
C0004096  |  asthma  |  1
C0023890  |  cirrhosis  |  1
C0042373  |  vascular disease  |  1
C0020502  |  hyperparathyroidism  |  1
C0017601  |  glaucoma  |  1
C0022661  |  end-stage renal disease  |  1
C0014868  |  esophagitis  |  1
C0022658  |  renal disease  |  1
C0043121  |  wernicke's encephalopathy  |  1
C0011847  |  diabetes  |  1
C0019360  |  zoster  |  1
C0019284  |  diaphragmatic hernia  |  1
C0010068  |  coronary heart disease  |  1
C0014869  |  reflux esophagitis  |  1
C0085096  |  peripheral vascular disease  |  1
C0600260  |  obstructive pulmonary disease  |  1
C0011849  |  diabetes mellitus  |  1
C0008350  |  gallstones  |  1
C0017612  |  open angle glaucoma  |  1
C0030920  |  peptic ulcer  |  1
C0010068  |  coronary artery disease  |  1
C0003467  |  anxiety  |  1
C0018799  |  heart disease  |  1
C0030305  |  pancreatitis  |  1
C0024115  |  pulmonary disease  |  1
C0339573  |  primary open angle glaucoma  |  1
C0005586  |  bipolar disorder  |  1
C0024117  |  chronic obstructive pulmonary disease  |  1
Curated Gene
Entrez_id | Symbol | Resource(Total Genes:3)
EDN1  |  1906  |  CTD_human
IL1B  |  3553  |  CTD_human
GAST  |  2520  |  CTD_human
Inferring Gene
Entrez_id | Symbol | Resource(Total Genes:3)
3593  |  IL12B  |  infer
4780  |  NFE2L2  |  infer
5742  |  PTGS1  |  infer
Text Mined Gene
Entrez_id | Symbol | Score | Resource(Total Genes:170)
6343  |  SCT  |  DISEASES
4710  |  NDUFB4  |  DISEASES
27248  |  ERLEC1  |  DISEASES
9812  |  KIAA0141  |  DISEASES
28954  |  REM1  |  DISEASES
3002  |  GZMB  |  DISEASES
1113  |  CHGA  |  DISEASES
479  |  ATP12A  |  DISEASES
2137  |  EXTL3  |  DISEASES
973  |  CD79A  |  DISEASES
1048  |  CEACAM5  |  DISEASES
10392  |  NOD1  |  DISEASES
4353  |  MPO  |  DISEASES
6347  |  CCL2  |  DISEASES
5539  |  PPY  |  DISEASES
3558  |  IL2  |  DISEASES
3565  |  IL4  |  DISEASES
56920  |  SEMA3G  |  DISEASES
4953  |  ODC1  |  DISEASES
8574  |  AKR7A2  |  DISEASES
1958  |  EGR1  |  DISEASES
654231  |  OCM  |  DISEASES
54210  |  TREM1  |  DISEASES
3306  |  HSPA2  |  DISEASES
7425  |  VGF  |  DISEASES
968  |  CD68  |  DISEASES
3630  |  INS  |  DISEASES
9945  |  GFPT2  |  DISEASES
1401  |  CRP  |  DISEASES
4922  |  NTS  |  DISEASES
78986  |  DUSP26  |  DISEASES
2922  |  GRP  |  DISEASES
2694  |  GIF  |  DISEASES
4951  |  OCM2  |  DISEASES
26122  |  EPC2  |  DISEASES
3569  |  IL6  |  DISEASES
3557  |  IL1RN  |  DISEASES
7097  |  TLR2  |  DISEASES
1559  |  CYP2C9  |  DISEASES
9360  |  PPIG  |  DISEASES
7450  |  VWF  |  DISEASES
384  |  ARG2  |  DISEASES
6521  |  SLC4A1  |  DISEASES
495  |  ATP4A  |  DISEASES
25939  |  SAMHD1  |  DISEASES
8578  |  SCARF1  |  DISEASES
3553  |  IL1B  |  DISEASES
23476  |  BRD4  |  DISEASES
3938  |  LCT  |  DISEASES
2247  |  FGF2  |  DISEASES
5443  |  POMC  |  DISEASES
1950  |  EGF  |  DISEASES
7157  |  TP53  |  DISEASES
7462  |  LAT2  |  DISEASES
1392  |  CRH  |  DISEASES
3176  |  HNMT  |  DISEASES
3606  |  IL18  |  DISEASES
5805  |  PTS  |  DISEASES
5741  |  PTH  |  DISEASES
152273  |  FGD5  |  DISEASES
6750  |  SST  |  DISEASES
3815  |  KIT  |  DISEASES
7032  |  TFF2  |  DISEASES
7031  |  TFF1  |  DISEASES
114757  |  CYGB  |  DISEASES
51127  |  TRIM17  |  DISEASES
389015  |  SLC9A4  |  DISEASES
886  |  CCKAR  |  DISEASES
10109  |  ARPC2  |  DISEASES
152185  |  SPICE1  |  DISEASES
213  |  ALB  |  DISEASES
8642  |  DCHS1  |  DISEASES
5479  |  PPIB  |  DISEASES
6447  |  SCG5  |  DISEASES
8000  |  PSCA  |  DISEASES
5617  |  PRL  |  DISEASES
7200  |  TRH  |  DISEASES
5066  |  PAM  |  DISEASES
125  |  ADH1B  |  DISEASES
200558  |  APLF  |  DISEASES
54498  |  SMOX  |  DISEASES
2147  |  F2  |  DISEASES
5340  |  PLG  |  DISEASES
5222  |  PGA5  |  DISEASES
6868  |  ADAM17  |  DISEASES
947  |  CD34  |  DISEASES
132243  |  H1FOO  |  DISEASES
6863  |  TAC1  |  DISEASES
85302  |  FBF1  |  DISEASES
4843  |  NOS2  |  DISEASES
7485  |  WRB  |  DISEASES
2520  |  GAST  |  DISEASES
796  |  CALCA  |  DISEASES
8338  |  HIST2H2AC  |  DISEASES
220323  |  OAF  |  DISEASES
2152  |  F3  |  DISEASES
55589  |  BMP2K  |  DISEASES
51738  |  GHRL  |  DISEASES
887  |  CCKBR  |  DISEASES
885  |  CCK  |  DISEASES
4221  |  MEN1  |  DISEASES
3117  |  HLA-DQA1  |  DISEASES
875  |  CBS  |  DISEASES
100506658  |  OCLN  |  DISEASES
5265  |  SERPINA1  |  DISEASES
2695  |  GIP  |  DISEASES
1510  |  CTSE  |  DISEASES
26136  |  TES  |  DISEASES
5697  |  PYY  |  DISEASES
3360  |  HTR4  |  DISEASES
56477  |  CCL28  |  DISEASES
5742  |  PTGS1  |  DISEASES
9760  |  TOX  |  DISEASES
4513  |  MT-CO2  |  DISEASES
9926  |  LPGAT1  |  DISEASES
5743  |  PTGS2  |  DISEASES
6279  |  S100A8  |  DISEASES
8337  |  HIST2H2AA3  |  DISEASES
23195  |  MDN1  |  DISEASES
2316  |  FLNA  |  DISEASES
959  |  CD40LG  |  DISEASES
1557  |  CYP2C19  |  DISEASES
7422  |  VEGFA  |  DISEASES
5225  |  PGC  |  DISEASES
5292  |  PIM1  |  DISEASES
286205  |  SCAI  |  DISEASES
7099  |  TLR4  |  DISEASES
3118  |  HLA-DQA2  |  DISEASES
8859  |  STK19  |  DISEASES
2155  |  F7  |  DISEASES
3303  |  HSPA1A  |  DISEASES
3305  |  HSPA1L  |  DISEASES
3055  |  HCK  |  DISEASES
9576  |  SPAG6  |  DISEASES
23412  |  COMMD3  |  DISEASES
3274  |  HRH2  |  DISEASES
79135  |  APOO  |  DISEASES
1906  |  EDN1  |  DISEASES
1045  |  CDX2  |  DISEASES
402682  |  UFSP1  |  DISEASES
94  |  ACVRL1  |  DISEASES
6370  |  CCL25  |  DISEASES
2962  |  GTF2F1  |  DISEASES
1365  |  CLDN3  |  DISEASES
65010  |  SLC26A6  |  DISEASES
79924  |  ADM2  |  DISEASES
2919  |  CXCL1  |  DISEASES
594857  |  NPS  |  DISEASES
2950  |  GSTP1  |  DISEASES
2641  |  GCG  |  DISEASES
4295  |  MLN  |  DISEASES
7124  |  TNF  |  DISEASES
7866  |  IFRD2  |  DISEASES
9228  |  DLGAP2  |  DISEASES
4049  |  LTA  |  DISEASES
4588  |  MUC6  |  DISEASES
389125  |  MUSTN1  |  DISEASES
3586  |  IL10  |  DISEASES
4583  |  MUC2  |  DISEASES
7884  |  SLBP  |  DISEASES
10772  |  SRSF10  |  DISEASES
131  |  ADH7  |  DISEASES
4008  |  LMO7  |  DISEASES
4586  |  MUC5AC  |  DISEASES
26298  |  EHF  |  DISEASES
142891  |  SAMD8  |  DISEASES
246744  |  STH  |  DISEASES
8972  |  MGAM  |  DISEASES
51741  |  WWOX  |  DISEASES
102723508  |  KANTR  |  DISEASES
Locus(Waiting for update.)
Disease ID 828
Disease peptic ulcer disease
Integrated Phenotype(Waiting for update.)
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:28)
HP:0012126  |  Gastric cancer  |  6
HP:0002239  |  Gastrointestinal hemorrhage  |  3
HP:0002584  |  Intestinal hemorrhage  |  3
HP:0012531  |  Pain  |  2
HP:0005231  |  Chronic gastritis  |  2
HP:0005263  |  Gastritis  |  2
HP:0100633  |  Inflammation of the esophagus  |  1
HP:0000819  |  Diabetes mellitus  |  1
HP:0100790  |  Hernia  |  1
HP:0007302  |  Bipolar disorder  |  1
HP:0001394  |  Hepatic cirrhosis  |  1
HP:0002099  |  Asthma  |  1
HP:0006510  |  Chronic obstructive pulmonary disease  |  1
HP:0012108  |  Primary open angle glaucoma  |  1
HP:0000843  |  Hyperparathyroidism  |  1
HP:0003774  |  End-stage renal failure  |  1
HP:0001677  |  Coronary artery disease  |  1
HP:0000501  |  Glaucoma  |  1
HP:0000739  |  Anxiety  |  1
HP:0001945  |  Fever  |  1
HP:0002024  |  Intestinal malabsorption  |  1
HP:0005202  |  Helicobacter pylori infection  |  1
HP:0004398  |  Peptic ulcer  |  1
HP:0100867  |  Duodenal stenosis/atresia  |  1
HP:0001298  |  Encephalopathy  |  1
HP:0001081  |  Gallstones  |  1
HP:0000776  |  Diaphragmatic hernia  |  1
HP:0001733  |  Pancreatic inflammation  |  1
Disease ID 828
Disease peptic ulcer disease
Manually Symptom(Waiting for update.)
Text Mined Symptom
UMLS | Name | Sentences' Count(Total Symptoms:9)
C0009450  |  infection  |  7
C0024623  |  gastric cancer  |  6
C0267373  |  intestinal bleeding  |  3
C0001173  |  gastric outlet obstruction  |  2
C0017152  |  gastritis  |  2
C0014868  |  esophagitis  |  1
C0850666  |  h. pylori infection  |  1
C0267055  |  erosive esophagitis  |  1
C0850666  |  helicobacter pylori infection  |  1
Manually Genotype(Total Text Mining Genotypes:0)
(Waiting for update.)
All Snps(Total Genotypes:22)
snpId pubmedId geneId geneSymbol diseaseId sourceId sentence score Year geneSymbol_dbSNP CHROMOSOME POS REF ALT
rs10306114170780015742PTGS1umls:C0030920BeFreeThe COX-1 A-842G/C50T SNP does not influence the risk for developing peptic ulcer bleeding.0.0084583052006PTGS19122370243AG
rs1045642186443895243ABCB1umls:C0030920BeFreeMDR1 C3435T polymorphism has no influence on developing Helicobacter pylori infection-related gastric cancer and peptic ulcer in Japanese.0.0087297472008ABCB1787509329AT,G
rs1045642248154415243ABCB1umls:C0030920BeFreeLack of association of the MDR1 C3435T polymorphism with susceptibility to gastric cancer and peptic ulcer: a systemic review and meta-analysis.0.0087297472015ABCB1787509329AT,G
rs1045642220019875243ABCB1umls:C0030920BeFreeC3435T polymorphism of the ABCB1 gene: impact on genetic susceptibility to peptic ulcers.0.0087297472011ABCB1787509329AT,G
rs10509681232678571559CYP2C9umls:C0030920BeFreeWe investigated whether eight functional SNPs in the CYP2C family of genes--CYP2C8*3 (rs11572080 and rs10509681), CYP2C8*4, CYP2C9*2, CYP2C9*3, CYP2C19*2, CYP2C19*3, and CYP2C19*17--are associated with PUD in 1,239 Caucasian patients.0.0052769482013CYP2C81095038992TC
rs10509681232678571558CYP2C8umls:C0030920BeFreeWe investigated whether eight functional SNPs in the CYP2C family of genes--CYP2C8*3 (rs11572080 and rs10509681), CYP2C8*4, CYP2C9*2, CYP2C9*3, CYP2C19*2, CYP2C19*3, and CYP2C19*17--are associated with PUD in 1,239 Caucasian patients.0.0002714422013CYP2C81095038992TC
rs11572080232678571559CYP2C9umls:C0030920BeFreeWe investigated whether eight functional SNPs in the CYP2C family of genes--CYP2C8*3 (rs11572080 and rs10509681), CYP2C8*4, CYP2C9*2, CYP2C9*3, CYP2C19*2, CYP2C19*3, and CYP2C19*17--are associated with PUD in 1,239 Caucasian patients.0.0052769482013CYP2C81095067273CT
rs11572080232678571558CYP2C8umls:C0030920BeFreeWe investigated whether eight functional SNPs in the CYP2C family of genes--CYP2C8*3 (rs11572080 and rs10509681), CYP2C8*4, CYP2C9*2, CYP2C9*3, CYP2C19*2, CYP2C19*3, and CYP2C19*17--are associated with PUD in 1,239 Caucasian patients.0.0002714422013CYP2C81095067273CT
rs1161491321073609406938MIR146Aumls:C0030920BeFreeWe evaluated the associations of three SNPs (rs11614913, rs2910164, and rs3746444) in pre-miRNAs (miR-196a2, miR-146a, and miR-499) with the risk of gastric cancer (GC) and peptic ulcer diseases, and with the severity of Helicobacter pylori-induced gastritis in Japanese population.0.0002714422010MIR196A21253991815CT
rs1161491321073609574501MIR499Aumls:C0030920BeFreeWe evaluated the associations of three SNPs (rs11614913, rs2910164, and rs3746444) in pre-miRNAs (miR-196a2, miR-146a, and miR-499) with the risk of gastric cancer (GC) and peptic ulcer diseases, and with the severity of Helicobacter pylori-induced gastritis in Japanese population.0.0002714422010MIR196A21253991815CT
rs1330344252431615742PTGS1umls:C0030920BeFreeImpact of blood type, functional polymorphism (T-1676C) of the COX-1 gene promoter and clinical factors on the development of peptic ulcer during cardiovascular prophylaxis with low-dose aspirin.0.0084583052014PTGS19122369409CT
rs1799964253687517124TNFumls:C0030920BeFreeTNFA-308G>A (rs1800629) and TNFA-1031T>C (rs1799964), which are responsible for increased TNFA transcription, could influence the risk of peptic ulceration.0.0167310452013LTA;TNF;LOC100287329631574531TC
rs1800629253687517124TNFumls:C0030920BeFreeTNFA-308G>A (rs1800629) and TNFA-1031T>C (rs1799964), which are responsible for increased TNFA transcription, could influence the risk of peptic ulceration.0.0167310452013TNF631575254GA
rs1801282183722845468PPARGumls:C0030920BeFreeThe study suggests that Pro12Ala PPARgamma polymorphism is associated with gastric adenocarcinoma and PUD, and is a potential marker for genetic susceptibility to these two diseases in the presence of H. pylori infection.0.0053628242008PPARG312351626CG
rs1805192183722845468PPARGumls:C0030920BeFreeThe study suggests that Pro12Ala PPARgamma polymorphism is associated with gastric adenocarcinoma and PUD, and is a potential marker for genetic susceptibility to these two diseases in the presence of H. pylori infection.0.0053628242008PPARG312379739CG
rs2075820173097487099TLR4umls:C0030920BeFreeE266K CARD4/NOD1, but not the TLR4 gene polymorphism increases the risk of peptic ulceration in H. pylori-positive patients.0.0002714422007NOD1730452621CT
rs20758201730974810392NOD1umls:C0030920BeFreeE266K CARD4/NOD1, but not the TLR4 gene polymorphism increases the risk of peptic ulceration in H. pylori-positive patients.0.0005428842007NOD1730452621CT
rs291016421073609406938MIR146Aumls:C0030920BeFreeWe evaluated the associations of three SNPs (rs11614913, rs2910164, and rs3746444) in pre-miRNAs (miR-196a2, miR-146a, and miR-499) with the risk of gastric cancer (GC) and peptic ulcer diseases, and with the severity of Helicobacter pylori-induced gastritis in Japanese population.0.0002714422010LOC285628;MIR146A5160485411CG
rs291016421073609574501MIR499Aumls:C0030920BeFreeWe evaluated the associations of three SNPs (rs11614913, rs2910164, and rs3746444) in pre-miRNAs (miR-196a2, miR-146a, and miR-499) with the risk of gastric cancer (GC) and peptic ulcer diseases, and with the severity of Helicobacter pylori-induced gastritis in Japanese population.0.0002714422010LOC285628;MIR146A5160485411CG
rs374644421073609574501MIR499Aumls:C0030920BeFreeWe evaluated the associations of three SNPs (rs11614913, rs2910164, and rs3746444) in pre-miRNAs (miR-196a2, miR-146a, and miR-499) with the risk of gastric cancer (GC) and peptic ulcer diseases, and with the severity of Helicobacter pylori-induced gastritis in Japanese population.0.0002714422010MYH7B;MIR499A;MIR499B2034990448AG
rs374644421073609406938MIR146Aumls:C0030920BeFreeWe evaluated the associations of three SNPs (rs11614913, rs2910164, and rs3746444) in pre-miRNAs (miR-196a2, miR-146a, and miR-499) with the risk of gastric cancer (GC) and peptic ulcer diseases, and with the severity of Helicobacter pylori-induced gastritis in Japanese population.0.0002714422010MYH7B;MIR499A;MIR499B2034990448AG
rs3842787170780015742PTGS1umls:C0030920BeFreeThe COX-1 A-842G/C50T SNP does not influence the risk for developing peptic ulcer bleeding.0.0084583052006PTGS19122371228CT
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:13)
CUI ChemicalName ChemicalID CasRN DiseaseName DiseaseID DirectEvidence PubMedIDs
C0030920atropineD00128551-55-8peptic ulcerMESH:D010437therapeutic7034155
C0030920celecoxibD000068579-peptic ulcerMESH:D010437marker/mechanism16897817
C0030920cimetidineD00292751481-61-9peptic ulcerMESH:D010437therapeutic11421865
C0030920diclofenacD00400815307-86-5peptic ulcerMESH:D010437marker/mechanism16897817
C0030920indomethacinD00721353-86-1peptic ulcerMESH:D010437marker/mechanism11148446
C0030920lansoprazoleD064747-peptic ulcerMESH:D010437therapeutic11394734
C0030920omeprazoleD00985373590-58-6peptic ulcerMESH:D010437marker/mechanism8667442
C0030920omeprazoleD00985373590-58-6peptic ulcerMESH:D010437therapeutic10192720
C0030920pantoprazoleC064276102625-70-7peptic ulcerMESH:D010437therapeutic19837071
C0030920piroxicamD01089436322-90-4peptic ulcerMESH:D010437marker/mechanism2957207
C0030920spironolactoneD0131481952/1/7peptic ulcerMESH:D010437therapeutic5569832
C0030920sucralfateD01339254182-58-0peptic ulcerMESH:D010437marker/mechanism8667442
C0030920tinidazoleD01401119387-91-8peptic ulcerMESH:D010437therapeutic11394734
FDA approved drug and dosage information(Total Drugs:0)
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FDA labeling changes(Total Drugs:0)
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