Home Contact Sitemap

PedAM

Pediatric Disease Annotations & Medicines



   hepatitis a
  

Disease ID 775
Disease hepatitis a
Definition
INFLAMMATION of the LIVER in humans caused by a member of the HEPATOVIRUS genus, HUMAN HEPATITIS A VIRUS. It can be transmitted through fecal contamination of food or water.
Synonym
a hepatitis
hav
hep a
hep a, nos
hepatitides, infectious
hepatitis a [disease/finding]
hepatitis a infection
hepatitis infect
hepatitis infectious
hepatitis viral
hepatitis, infectious
ih - infectious hepatitis
infect hepatitis
infectious hepatitides
infectious hepatitis
infectious hepatitis (disorder)
infectious hepatitis (hepatitis a)
infectious hepatitis a
infectious viral hepatitis
viral hepatitis, type a
viral hepatitis, type a (disorder)
DOID
UMLS
C0019159
MeSH
SNOMED-CT
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:139)
C0023895  |  liver disease  |  27
C0023890  |  cirrhosis  |  20
C0019158  |  hepatitis  |  15
C0008370  |  cholestasis  |  11
C0019163  |  hepatitis b  |  11
C0023890  |  liver cirrhosis  |  8
C0034362  |  q fever  |  6
C0008049  |  varicella  |  5
C0023895  |  liver diseases  |  4
C0948265  |  metabolic syndrome  |  4
C0002871  |  anemia  |  4
C0019196  |  hepatitis c  |  4
C0007570  |  celiac disease  |  4
C0002878  |  hemolytic anemia  |  4
C0022660  |  acute renal failure  |  4
C0035078  |  renal failure  |  4
C0008325  |  cholecystitis  |  3
C0085293  |  hepatitis e  |  3
C0024299  |  lymphoma  |  3
C0042769  |  virus infection  |  3
C0001339  |  acute pancreatitis  |  3
C0281963  |  red cell aplasia  |  3
C0034902  |  pure red cell aplasia  |  3
C0019204  |  hepatocellular carcinoma  |  2
C0023434  |  chronic lymphocytic leukemia  |  2
C0030305  |  pancreatitis  |  2
C0008312  |  primary biliary cirrhosis  |  2
C0085253  |  adult-onset still disease  |  2
C0042721  |  viral hepatitis  |  2
C0024314  |  lymphoproliferative disorder  |  2
C0033860  |  psoriasis  |  2
C0017152  |  gastritis  |  2
C0041466  |  typhoid fever  |  2
C0018799  |  heart disease  |  2
C0034150  |  purpura  |  2
C0006309  |  brucellosis  |  2
C0267841  |  acalculous cholecystitis  |  2
C0042769  |  viral infection  |  2
C0241910  |  autoimmune hepatitis  |  2
C0023448  |  lymphocytic leukemia  |  2
C0008312  |  biliary cirrhosis  |  2
C0002880  |  autoimmune hemolytic anemia  |  2
C0011847  |  diabetes  |  2
C0006142  |  breast cancer  |  1
C0019360  |  zoster  |  1
C0024291  |  hemophagocytic syndrome  |  1
C0021390  |  inflammatory bowel disease  |  1
C0085273  |  parvovirus b19 infection  |  1
C0024198  |  lyme disease  |  1
C0026934  |  mycoplasma  |  1
C0037315  |  sleep apnea  |  1
C0152445  |  gallbladder hydrops  |  1
C0021831  |  bowel disease  |  1
C0042384  |  vasculitis  |  1
C0001125  |  lactic acidosis  |  1
C0002892  |  pernicious anemia  |  1
C0004096  |  asthma  |  1
C0035333  |  retinitis  |  1
C0235974  |  pancreas cancer  |  1
C0018801  |  heart failure  |  1
C0034152  |  henoch-schoenlein purpura  |  1
C0011570  |  depression  |  1
C0035435  |  rheumatic disease  |  1
C0079744  |  diffuse large b-cell lymphoma  |  1
C0023895  |  liver disorders  |  1
C0025286  |  meningioma  |  1
C0019204  |  hepatoma  |  1
C0039614  |  tetanus  |  1
C0023418  |  leukemia  |  1
C0079731  |  b-cell lymphoma  |  1
C0022658  |  renal disease  |  1
C0025289  |  meningitis  |  1
C0015230  |  rash  |  1
C0008350  |  gallstones  |  1
C0032827  |  k deficiency  |  1
C0032026  |  pityriasis rosea  |  1
C0023895  |  liver disorder  |  1
C0021053  |  immune disease  |  1
C0279682  |  bladder adenocarcinoma  |  1
C0020538  |  hypertension  |  1
C0221032  |  generalized lipodystrophy  |  1
C0011854  |  type 1 diabetes  |  1
C0007131  |  nsclc  |  1
C0036421  |  systemic sclerosis  |  1
C0009782  |  connective tissue disease  |  1
C0017658  |  glomerulonephritis  |  1
C0206698  |  cholangiocarcinoma  |  1
C0041296  |  tuberculosis  |  1
C0036323  |  schistosomiasis  |  1
C0026272  |  mixed connective tissue disease  |  1
C0024790  |  paroxysmal nocturnal hemoglobinuria  |  1
C0035435  |  rheumatic diseases  |  1
C0019100  |  dengue haemorrhagic fever  |  1
C0001418  |  adenocarcinoma  |  1
C0376175  |  bell's palsy  |  1
C0020443  |  hypercholesterolemia  |  1
C0085253  |  adult onset still's disease  |  1
C0030528  |  paratyphoid  |  1
C0520679  |  obstructive sleep apnea  |  1
C0030528  |  paratyphoid fever  |  1
C0085273  |  erythema infectiosum  |  1
C0021359  |  infertile  |  1
C0006017  |  pertussis  |  1
C0022658  |  nephropathy  |  1
C0011849  |  diabetes mellitus  |  1
C0003873  |  rheumatoid arthritis  |  1
C0022602  |  actinic keratoses  |  1
C0025309  |  meningoencephalitis  |  1
C0019348  |  herpes simplex  |  1
C0012546  |  diphtheria  |  1
C1334028  |  hilar cholangiocarcinoma  |  1
C0011854  |  type 1 diabetes mellitus  |  1
C0039128  |  syphilis  |  1
C0043117  |  immune thrombocytopenic purpura  |  1
C0023787  |  lipodystrophy  |  1
C0002874  |  aplastic anemia  |  1
C0023343  |  leprosy  |  1
C0042109  |  urticaria  |  1
C0027697  |  nephritis  |  1
C0017665  |  membranous glomerulonephritis  |  1
C0019163  |  viral hepatitis b  |  1
C0032302  |  mycoplasma pneumonia  |  1
C0345905  |  intrahepatic cholangiocarcinoma  |  1
C0022354  |  cholestatic jaundice  |  1
C0036285  |  scarlet fever  |  1
C0029456  |  osteoporosis  |  1
C0041466  |  typhoid  |  1
C0085655  |  polymyositis  |  1
C0014038  |  encephalitis  |  1
C0740441  |  acute diarrhea  |  1
C0040053  |  thrombosis  |  1
C0023890  |  hepatic cirrhosis  |  1
C0403416  |  crescentic glomerulonephritis  |  1
C0006625  |  cachectic  |  1
C0032285  |  pneumoniae  |  1
C0028754  |  obesity  |  1
C0024314  |  lymphoproliferative disorders  |  1
C0025293  |  listeria monocytogenes meningitis  |  1
C0279651  |  gallbladder adenocarcinoma  |  1
Curated Gene(Waiting for update.)
Inferring Gene(Waiting for update.)
Text Mined Gene
Entrez_id | Symbol | Score | Resource(Total Genes:104)
10942  |  PRSS21  |  DISEASES
4710  |  NDUFB4  |  DISEASES
2158  |  F9  |  DISEASES
11151  |  CORO1A  |  DISEASES
2137  |  EXTL3  |  DISEASES
973  |  CD79A  |  DISEASES
3558  |  IL2  |  DISEASES
374291  |  NDUFS7  |  DISEASES
8574  |  AKR7A2  |  DISEASES
28981  |  IFT81  |  DISEASES
84329  |  HVCN1  |  DISEASES
514  |  ATP5E  |  DISEASES
2678  |  GGT1  |  DISEASES
5894  |  RAF1  |  DISEASES
2161  |  F12  |  DISEASES
3337  |  DNAJB1  |  DISEASES
26284  |  ERAL1  |  DISEASES
1401  |  CRP  |  DISEASES
3034  |  HAL  |  DISEASES
7450  |  VWF  |  DISEASES
22858  |  ICK  |  DISEASES
64135  |  IFIH1  |  DISEASES
84083  |  ZRANB3  |  DISEASES
10058  |  ABCB6  |  DISEASES
51608  |  GET4  |  DISEASES
56938  |  ARNTL2  |  DISEASES
51411  |  BIN2  |  DISEASES
80816  |  ASXL3  |  DISEASES
4864  |  NPC1  |  DISEASES
150094  |  SIK1  |  DISEASES
167410  |  LIX1  |  DISEASES
4715  |  NDUFB9  |  DISEASES
3439  |  IFNA1  |  DISEASES
23082  |  PPRC1  |  DISEASES
636  |  BICD1  |  DISEASES
50848  |  F11R  |  DISEASES
8209  |  C21orf33  |  DISEASES
4056  |  LTC4S  |  DISEASES
3046  |  HBE1  |  DISEASES
248  |  ALPI  |  DISEASES
54738  |  FEV  |  DISEASES
213  |  ALB  |  DISEASES
81501  |  DCSTAMP  |  DISEASES
124935  |  SLC43A2  |  DISEASES
375611  |  SLC26A5  |  DISEASES
160065  |  PATE1  |  DISEASES
2147  |  F2  |  DISEASES
27243  |  CHMP2A  |  DISEASES
134083  |  OR2Y1  |  DISEASES
147912  |  SIX5  |  DISEASES
53347  |  UBASH3A  |  DISEASES
2744  |  GLS  |  DISEASES
149830  |  PRNT  |  DISEASES
6014  |  RIT2  |  DISEASES
2274  |  FHL2  |  DISEASES
3309  |  HSPA5  |  DISEASES
2152  |  F3  |  DISEASES
2182  |  ACSL4  |  DISEASES
9577  |  BRE  |  DISEASES
285193  |  DUSP28  |  DISEASES
10202  |  DHRS2  |  DISEASES
26762  |  HAVCR1  |  DISEASES
84706  |  GPT2  |  DISEASES
5265  |  SERPINA1  |  DISEASES
130013  |  ACMSD  |  DISEASES
6942  |  TCF20  |  DISEASES
2157  |  F8  |  DISEASES
4512  |  MT-CO1  |  DISEASES
58  |  ACTA1  |  DISEASES
462  |  SERPINC1  |  DISEASES
1805  |  DPT  |  DISEASES
10767  |  HBS1L  |  DISEASES
284486  |  THEM5  |  DISEASES
5654  |  HTRA1  |  DISEASES
4923  |  NTSR1  |  DISEASES
2805  |  GOT1  |  DISEASES
959  |  CD40LG  |  DISEASES
6406  |  SEMG1  |  DISEASES
55315  |  SLC29A3  |  DISEASES
4146  |  MATN1  |  DISEASES
55906  |  ZC4H2  |  DISEASES
2155  |  F7  |  DISEASES
23412  |  COMMD3  |  DISEASES
8718  |  TNFRSF25  |  DISEASES
170302  |  ARX  |  DISEASES
29103  |  DNAJC15  |  DISEASES
23586  |  DDX58  |  DISEASES
3030  |  HADHA  |  DISEASES
79866  |  BORA  |  DISEASES
250  |  ALPP  |  DISEASES
2875  |  GPT  |  DISEASES
174  |  AFP  |  DISEASES
728441  |  GGT2  |  DISEASES
1363  |  CPE  |  DISEASES
57703  |  CWC22  |  DISEASES
197  |  AHSG  |  DISEASES
7124  |  TNF  |  DISEASES
57506  |  MAVS  |  DISEASES
10046  |  MAMLD1  |  DISEASES
629  |  CFB  |  DISEASES
2533  |  FYB  |  DISEASES
10846  |  PDE10A  |  DISEASES
51667  |  NUB1  |  DISEASES
246734  |  NPCDR1  |  DISEASES
Locus(Waiting for update.)
Disease ID 775
Disease hepatitis a
Integrated Phenotype(Waiting for update.)
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:105)
HP:0001394  |  Hepatic cirrhosis  |  20
HP:0001399  |  Liver failure  |  19
HP:0012115  |  Liver inflammation  |  16
HP:0001397  |  Hepatic steatosis  |  15
HP:0001945  |  Fever  |  14
HP:0001396  |  Cholestasis  |  11
HP:0200123  |  Chronic liver inflammation  |  10
HP:0001919  |  Acute renal failure  |  9
HP:0000952  |  Yellow skin  |  7
HP:0012531  |  Pain  |  4
HP:0200119  |  Acute liver inflammation  |  4
HP:0000083  |  Renal insufficiency  |  4
HP:0006554  |  Acute hepatic failure  |  4
HP:0002608  |  Celiac disease  |  4
HP:0001903  |  Anemia  |  4
HP:0002202  |  Pleural effusion  |  3
HP:0002960  |  Autoimmune condition  |  3
HP:0001878  |  Haemolytic anaemia  |  3
HP:0004448  |  Fulminant hepatic failure  |  3
HP:0002665  |  Lymphoma  |  3
HP:0012410  |  Pure red cell aplasia  |  3
HP:0001082  |  Cholecystitis  |  3
HP:0005523  |  Lymphoproliferative disorder  |  2
HP:0001402  |  Hepatocellular carcinoma  |  2
HP:0006562  |  Viral hepatitis  |  2
HP:0005550  |  Chronic lymphatic leukemia  |  2
HP:0005110  |  Atrial fibrillation  |  2
HP:0004787  |  Fulminant hepatitis  |  2
HP:0005263  |  Gastritis  |  2
HP:0003287  |  Abnormality of mitochondrial metabolism  |  2
HP:0001735  |  Acute pancreatitis  |  2
HP:0001733  |  Pancreatic inflammation  |  2
HP:0002613  |  Biliary cirrhosis  |  2
HP:0000855  |  Insulin resistance  |  2
HP:0001890  |  Autoimmune hemolytic anemia  |  2
HP:0003493  |  Elevated antinuclear antibody  |  2
HP:0000979  |  Purpura  |  2
HP:0001371  |  Flexion contractures of joints  |  1
HP:0030153  |  Cholangiocarcinoma  |  1
HP:0001030  |  Fragile skin  |  1
HP:0002858  |  Mengiomia  |  1
HP:0010535  |  Sleep apnea  |  1
HP:0001901  |  Abnormally shaped erythrocytes  |  1
HP:0001025  |  Hives  |  1
HP:0001404  |  Hepatocellular necrosis  |  1
HP:0002383  |  Encephalitis  |  1
HP:0001298  |  Encephalopathy  |  1
HP:0001915  |  Aplastic anemia  |  1
HP:0012191  |  B-cell lymphoma  |  1
HP:0000123  |  Nephritis  |  1
HP:0009064  |  Generalized lipodystrophy  |  1
HP:0012578  |  Membranous glomerulonephritis  |  1
HP:0001941  |  acidemia  |  1
HP:0030731  |  Carcinoma  |  1
HP:0002955  |  Granulomatosis  |  1
HP:0000112  |  Nephropathy  |  1
HP:0003128  |  Lactic acidosis  |  1
HP:0003002  |  Breast carcinoma  |  1
HP:0002910  |  Elevated transaminases  |  1
HP:0004420  |  Arterial thrombosis  |  1
HP:0002027  |  Abdominal pain  |  1
HP:0000989  |  pruritis  |  1
HP:0003124  |  Elevated serum cholesterol  |  1
HP:0009125  |  Lipodystrophy  |  1
HP:0002104  |  Absence of spontaneous respiration  |  1
HP:0010628  |  Facial palsy, unilateral or bilateral  |  1
HP:0100749  |  Thoracic pain  |  1
HP:0001370  |  Rheumatoid arthritis  |  1
HP:0001287  |  Meningitis  |  1
HP:0002633  |  Vasculitis  |  1
HP:0001250  |  Seizures  |  1
HP:0001513  |  Obesity  |  1
HP:0007256  |  Abnormal pyramidal signs  |  1
HP:0003765  |  Psoriasis  |  1
HP:0011675  |  Arrhythmias  |  1
HP:0000939  |  Osteoporosis  |  1
HP:0001081  |  Gallstones  |  1
HP:0010783  |  Erythema  |  1
HP:0008198  |  Congenital hypoparathyroidism  |  1
HP:0003256  |  Coagulopathy  |  1
HP:0004818  |  Paroxysmal nocturnal hemoglobinuria  |  1
HP:0012190  |  T cell lymphoma  |  1
HP:0002099  |  Asthma  |  1
HP:0003201  |  Rhabdomyolysis  |  1
HP:0012156  |  Hemophagocytosis  |  1
HP:0000716  |  Depression  |  1
HP:0002870  |  Obstructive sleep apnea  |  1
HP:0000819  |  Diabetes mellitus  |  1
HP:0008653  |  Crescentic glomerulonephritis  |  1
HP:0010310  |  Chylothorax  |  1
HP:0000969  |  Dropsy  |  1
HP:0001880  |  Eosinophilia  |  1
HP:0001541  |  Ascites  |  1
HP:0001410  |  Decreased liver function  |  1
HP:0002018  |  Nausea  |  1
HP:0012378  |  Fatigue  |  1
HP:0100806  |  Sepsis  |  1
HP:0001909  |  Leukemia  |  1
HP:0000099  |  Glomerular nephritis  |  1
HP:0002240  |  Enlarged liver  |  1
HP:0000822  |  Hypertension  |  1
HP:0001395  |  Hepatic fibrosis  |  1
HP:0001635  |  Congestive heart failure  |  1
HP:0011892  |  Vitamin K deficiency  |  1
HP:0000572  |  Visual loss  |  1
Disease ID 775
Disease hepatitis a
Manually Symptom(Waiting for update.)
Text Mined Symptom
UMLS | Name | Sentences' Count(Total Symptoms:1)
C0009450  |  infection  |  1
Manually Genotype(Total Text Mining Genotypes:0)
(Waiting for update.)
All Snps(Total Genotypes:8)
snpId pubmedId geneId geneSymbol diseaseId sourceId sentence score Year geneSymbol_dbSNP CHROMOSOME POS REF ALT
rs1042522235644817157TP53umls:C0019159BeFreeSubgroup analyses by source of controls and hepatitis virus infection status further demonstrated the significant association, whereas stratification factors involving gender and family history of HCC did not modify the association between p53 codon 72 Arg/Pro polymorphism and HCC risk.0.0032573022013TP53177676154GT,C
rs10853728234691423627CXCL10umls:C0019159BeFreeIn HBeAg-positive patients (n = 48), HBV viral load correlated with active hepatitis, while in HBeAg-negative patients (n = 67), rs10853728 CC genotype (p = 0.032) and a trend of higher IP-10 levels (p = 0.092) were associated with active hepatitis.0.0008143262013NA1939254506CG,T
rs11540654235644817157TP53umls:C0019159BeFreeSubgroup analyses by source of controls and hepatitis virus infection status further demonstrated the significant association, whereas stratification factors involving gender and family history of HCC did not modify the association between p53 codon 72 Arg/Pro polymorphism and HCC risk.0.0032573022013TP53177676040CT,G,A
rs1297986024085431282617IFNL3umls:C0019159BeFreeIn the overall analysis, the IL-28B rs12979860 T/C polymorphism was identified as a genetic risk factor for hepatitis virus-related HCC and LC development.0.0016286512014IFNL3;IFNL41939248147CT
rs1297986025971683282617IFNL3umls:C0019159BeFreeDifferential distribution of IL28B.rs12979860 single-nucleotide polymorphism among Egyptian healthcare workers with and without a hepatitis C virus-specific cellular immune response.0.0016286512015IFNL3;IFNL41939248147CT
rs25487237808947515XRCC1umls:C0019159BeFreeOur meta-analysis of the available data did not find an obvious effect of XRCC1 Arg399Gln polymorphism on hepatitis-related hepatocellular carcinoma.0.0008143262013XRCC11943551574TC
rs386493716237808947515XRCC1umls:C0019159BeFreeOur meta-analysis of the available data did not find an obvious effect of XRCC1 Arg399Gln polymorphism on hepatitis-related hepatocellular carcinoma.0.0008143262013NANANANANA
rs386545618241552114524MTHFRumls:C0019159BeFreeAssociations between MTHFR Ala222Val polymorphism and risks of hepatitis and hepatitis-related liver cancer: a meta-analysis.0.0002714422013NANANANANA
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:1)
CUI ChemicalName ChemicalID CasRN DiseaseName DiseaseID DirectEvidence PubMedIDs
C0019159ribavirinD01225436791-04-5hepatitis aMESH:D006506therapeutic2167349
FDA approved drug and dosage information(Total Drugs:0)
(Waiting for update.)
FDA labeling changes(Total Drugs:0)
(Waiting for update.)