Home Contact Sitemap

eRAM

encyclopedia of Rare Disease Annotation for Precision Medicine



   viral hepatitis
  

Disease ID 1500
Disease viral hepatitis
Definition
Inflammation of the liver due to infection with a virus. [HPO:probinson]
Synonym
infectious hepatitis (viral hepatitis)
unspecified viral hepatitis
unspecified viral hepatitis (disorder)
vh - viral hepatitis
viral hepatitis (disorder)
viral hepatitis nos
viral hepatitis, nos
DOID
UMLS
C0042721
SNOMED-CT
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:85)
C0023890  |  cirrhosis  |  20
C0023895  |  liver disease  |  20
C0019204  |  hepatocellular carcinoma  |  7
C0019196  |  hepatitis c  |  5
C0001339  |  acute pancreatitis  |  4
C0023890  |  liver cirrhosis  |  4
C0002871  |  anemia  |  3
C0023903  |  liver cancer  |  3
C0019163  |  hepatitis b  |  3
C0008370  |  cholestasis  |  3
C0345905  |  intrahepatic cholangiocarcinoma  |  3
C0085293  |  hepatitis e  |  3
C0008325  |  cholecystitis  |  3
C0206698  |  cholangiocarcinoma  |  3
C0030305  |  pancreatitis  |  3
C0019158  |  hepatitis  |  2
C0002874  |  aplastic anemia  |  2
C0023895  |  liver diseases  |  2
C0267841  |  acalculous cholecystitis  |  2
C0036202  |  sarcoidosis  |  2
C0242350  |  erectile dysfunction  |  2
C0002892  |  pernicious anemia  |  1
C0024291  |  hemophagocytic syndrome  |  1
C0024314  |  lymphoproliferative disorder  |  1
C0041296  |  tuberculosis  |  1
C0023903  |  liver tumor  |  1
C0026975  |  myelitis  |  1
C0235974  |  pancreatic cancer  |  1
C0011991  |  diarrhoea  |  1
C0022661  |  end-stage renal disease  |  1
C0017658  |  glomerulonephritis  |  1
C0042769  |  virus infection  |  1
C0042769  |  viral disease  |  1
C0006142  |  breast cancer  |  1
C0011570  |  depression  |  1
C0026848  |  myopathies  |  1
C0011847  |  diabetes  |  1
C0002878  |  haemolytic anaemia  |  1
C0020532  |  hypersplenism  |  1
C0033860  |  psoriasis  |  1
C0030807  |  pemphigus  |  1
C0022658  |  renal disease  |  1
C0032285  |  pneumonia  |  1
C0024314  |  lymphoproliferative disorders  |  1
C0026764  |  myeloma  |  1
C0042870  |  vitamin d deficiency  |  1
C0021359  |  infertile  |  1
C0029106  |  opisthorchiasis  |  1
C0024299  |  lymphoma  |  1
C0010403  |  cryoglobulinemia  |  1
C0026764  |  multiple myeloma  |  1
C0034902  |  pure red cell aplasia  |  1
C0027813  |  neuritis  |  1
C0004626  |  bacterial pneumonia  |  1
C0010068  |  coronary artery disease  |  1
C0023418  |  leukemia  |  1
C0029134  |  optic neuritis  |  1
C0017920  |  glucose-6-phosphate dehydrogenase deficiency  |  1
C0281963  |  red cell aplasia  |  1
C0023434  |  chronic lymphocytic leukemia  |  1
C0020550  |  hyperthyroidism  |  1
C0178238  |  intestinal infection  |  1
C0032305  |  pneumocystis  |  1
C0042870  |  vitamin d defic  |  1
C0022658  |  kidney disease  |  1
C0152445  |  gallbladder hydrops  |  1
C0014868  |  esophagitis  |  1
C0011226  |  hepatitis d  |  1
C0032827  |  k deficiency  |  1
C0002871  |  anaemia  |  1
C1510472  |  drug addiction  |  1
C0023448  |  lymphocytic leukemia  |  1
C0011860  |  type 2 diabetes mellitus  |  1
C0018799  |  heart disease  |  1
C0018991  |  hemiplegia  |  1
C0003873  |  rheumatoid disease  |  1
C0036323  |  schistosomiasis  |  1
C0024301  |  follicular lymphoma  |  1
C0011860  |  type 2 diabetes  |  1
C0011849  |  diabetes mellitus  |  1
C0042769  |  viral infection  |  1
C0029456  |  osteoporosis  |  1
C0022350  |  dubin-johnson syndrome  |  1
C0442874  |  neuropathy  |  1
C0027121  |  inflammatory myopathies  |  1
Curated Gene(Waiting for update.)
Inferring Gene(Waiting for update.)
Text Mined Gene
Entrez_id | Symbol | Score | Resource(Total Genes:135)
2  |  A2M  |  2.129  |  DISEASES
58  |  ACTA1  |  1.654  |  DISEASES
203102  |  ADAM32  |  2.948  |  DISEASES
101  |  ADAM8  |  2.765  |  DISEASES
130  |  ADH6  |  1.173  |  DISEASES
9370  |  ADIPOQ  |  1.503  |  DISEASES
174  |  AFP  |  5.054  |  DISEASES
197  |  AHSG  |  1.115  |  DISEASES
1645  |  AKR1C1  |  2.244  |  DISEASES
1646  |  AKR1C2  |  2.256  |  DISEASES
229  |  ALDOB  |  1.884  |  DISEASES
567  |  B2M  |  2.211  |  DISEASES
29994  |  BAZ2B  |  2.143  |  DISEASES
632  |  BGLAP  |  1.004  |  DISEASES
9254  |  CACNA2D2  |  1.115  |  DISEASES
846  |  CASR  |  1.232  |  DISEASES
414062  |  CCL3L3  |  1.22  |  DISEASES
912  |  CD1D  |  1.318  |  DISEASES
958  |  CD40  |  1.258  |  DISEASES
959  |  CD40LG  |  5.787  |  DISEASES
9308  |  CD83  |  1.524  |  DISEASES
942  |  CD86  |  1.616  |  DISEASES
79094  |  CHAC1  |  1.663  |  DISEASES
339390  |  CLEC4G  |  1.968  |  DISEASES
283420  |  CLEC9A  |  1.503  |  DISEASES
493753  |  COA5  |  2.783  |  DISEASES
1363  |  CPE  |  3.498  |  DISEASES
1378  |  CR1  |  1.146  |  DISEASES
1490  |  CTGF  |  1.306  |  DISEASES
4283  |  CXCL9  |  1.549  |  DISEASES
2833  |  CXCR3  |  1.756  |  DISEASES
1544  |  CYP1A2  |  1.895  |  DISEASES
1565  |  CYP2D6  |  2.052  |  DISEASES
1576  |  CYP3A4  |  1.094  |  DISEASES
51428  |  DDX41  |  1.228  |  DISEASES
23586  |  DDX58  |  1.706  |  DISEASES
160851  |  DGKH  |  2.277  |  DISEASES
285193  |  DUSP28  |  2.867  |  DISEASES
1847  |  DUSP5  |  1.853  |  DISEASES
10209  |  EIF1  |  1.391  |  DISEASES
3692  |  EIF6  |  1.189  |  DISEASES
132884  |  EVC2  |  1.365  |  DISEASES
2152  |  F3  |  1.904  |  DISEASES
2155  |  F7  |  1.296  |  DISEASES
2157  |  F8  |  1.612  |  DISEASES
355  |  FAS  |  3.152  |  DISEASES
356  |  FASLG  |  3.106  |  DISEASES
2214  |  FCGR3A  |  1.151  |  DISEASES
23767  |  FLRT3  |  1.576  |  DISEASES
50943  |  FOXP3  |  1.778  |  DISEASES
2641  |  GCG  |  1.602  |  DISEASES
728441  |  GGT2  |  3.979  |  DISEASES
27333  |  GOLIM4  |  1.457  |  DISEASES
51280  |  GOLM1  |  1.724  |  DISEASES
2719  |  GPC3  |  1.525  |  DISEASES
2875  |  GPT  |  1.982  |  DISEASES
8971  |  H1FX  |  1.444  |  DISEASES
3030  |  HADHA  |  4.19  |  DISEASES
3043  |  HBB  |  1.575  |  DISEASES
3077  |  HFE  |  3.358  |  DISEASES
3009  |  HIST1H1B  |  1.015  |  DISEASES
3113  |  HLA-DPA1  |  2.264  |  DISEASES
3117  |  HLA-DQA1  |  1.613  |  DISEASES
3123  |  HLA-DRB1  |  1.551  |  DISEASES
3188  |  HNRNPH2  |  1.055  |  DISEASES
3240  |  HP  |  3.275  |  DISEASES
3339  |  HSPG2  |  1.279  |  DISEASES
3451  |  IFNA17  |  2.106  |  DISEASES
3440  |  IFNA2  |  3.68  |  DISEASES
3456  |  IFNB1  |  2.945  |  DISEASES
3586  |  IL10  |  2.618  |  DISEASES
3605  |  IL17A  |  1.194  |  DISEASES
3665  |  IRF7  |  1.412  |  DISEASES
10379  |  IRF9  |  2.55  |  DISEASES
9636  |  ISG15  |  1.07  |  DISEASES
3702  |  ITK  |  1.093  |  DISEASES
9622  |  KLK4  |  2.3  |  DISEASES
3821  |  KLRC1  |  1.019  |  DISEASES
3875  |  KRT18  |  2.291  |  DISEASES
3880  |  KRT19  |  2.027  |  DISEASES
3855  |  KRT7  |  1.775  |  DISEASES
246269  |  LACE1  |  1.356  |  DISEASES
3965  |  LGALS9  |  1.704  |  DISEASES
4017  |  LOXL2  |  1.134  |  DISEASES
116135  |  LRRC3B  |  1.365  |  DISEASES
57506  |  MAVS  |  1.061  |  DISEASES
259283  |  MDS2  |  1.366  |  DISEASES
10724  |  MGEA5  |  1.001  |  DISEASES
284424  |  MIR7-3HG  |  3.078  |  DISEASES
4312  |  MMP1  |  1.316  |  DISEASES
4599  |  MX1  |  2.319  |  DISEASES
4615  |  MYD88  |  1.374  |  DISEASES
259197  |  NCR3  |  1.047  |  DISEASES
57446  |  NDRG3  |  1.509  |  DISEASES
4739  |  NEDD9  |  2.092  |  DISEASES
4814  |  NINJ1  |  1.196  |  DISEASES
246734  |  NPCDR1  |  2.192  |  DISEASES
8504  |  PEX3  |  1.352  |  DISEASES
30814  |  PLA2G2E  |  1.978  |  DISEASES
5355  |  PLP2  |  1.407  |  DISEASES
26064  |  RAI14  |  1.648  |  DISEASES
6014  |  RIT2  |  3.411  |  DISEASES
56254  |  RNF20  |  1.25  |  DISEASES
51091  |  SEPSECS  |  2.735  |  DISEASES
5265  |  SERPINA1  |  3.305  |  DISEASES
12  |  SERPINA3  |  1.164  |  DISEASES
6906  |  SERPINA7  |  1.015  |  DISEASES
6318  |  SERPINB4  |  1.438  |  DISEASES
462  |  SERPINC1  |  2.11  |  DISEASES
10864  |  SLC22A7  |  1.648  |  DISEASES
94161  |  SNORD46  |  1.076  |  DISEASES
26800  |  SNORD49A  |  2.401  |  DISEASES
8651  |  SOCS1  |  1.468  |  DISEASES
9021  |  SOCS3  |  1.077  |  DISEASES
6654  |  SOS1  |  1.775  |  DISEASES
54558  |  SPATA6  |  1.581  |  DISEASES
6736  |  SRY  |  1.215  |  DISEASES
6772  |  STAT1  |  2.834  |  DISEASES
23336  |  SYNM  |  1.32  |  DISEASES
6938  |  TCF12  |  1.578  |  DISEASES
26136  |  TES  |  1.001  |  DISEASES
7018  |  TF  |  3.393  |  DISEASES
7056  |  THBD  |  1.578  |  DISEASES
284486  |  THEM5  |  1.601  |  DISEASES
7099  |  TLR4  |  1.585  |  DISEASES
51284  |  TLR7  |  2.107  |  DISEASES
54106  |  TLR9  |  1.669  |  DISEASES
53345  |  TM6SF2  |  1.947  |  DISEASES
7124  |  TNF  |  3.831  |  DISEASES
7133  |  TNFRSF1B  |  1.094  |  DISEASES
8718  |  TNFRSF25  |  2.517  |  DISEASES
7318  |  UBA7  |  1.004  |  DISEASES
7360  |  UGP2  |  2.711  |  DISEASES
55665  |  URGCP  |  1.171  |  DISEASES
220001  |  VWCE  |  1.679  |  DISEASES
Locus(Waiting for update.)
Disease ID 1500
Disease viral hepatitis
Integrated Phenotype(Waiting for update.)
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:69)
HP:0001394  |  Hepatic cirrhosis  |  24
HP:0001399  |  Liver failure  |  10
HP:0001402  |  Hepatocellular carcinoma  |  8
HP:0030731  |  Carcinoma  |  8
HP:0002896  |  Liver cancer  |  4
HP:0001903  |  Anemia  |  4
HP:0001733  |  Pancreatic inflammation  |  3
HP:0006554  |  Acute hepatic failure  |  3
HP:0001410  |  Decreased liver function  |  3
HP:0030153  |  Cholangiocarcinoma  |  3
HP:0001735  |  Acute pancreatitis  |  3
HP:0001082  |  Cholecystitis  |  3
HP:0004448  |  Fulminant hepatic failure  |  3
HP:0000802  |  Erectile dysfunction  |  2
HP:0001915  |  Aplastic anemia  |  2
HP:0100626  |  Chronic hepatic failure  |  2
HP:0001397  |  Hepatic steatosis  |  2
HP:0001395  |  Hepatic fibrosis  |  2
HP:0200123  |  Chronic liver inflammation  |  2
HP:0001396  |  Cholestasis  |  2
HP:0012115  |  Liver inflammation  |  2
HP:0000855  |  Insulin resistance  |  2
HP:0002960  |  Autoimmune condition  |  2
HP:0002716  |  Lymph node hyperplasia  |  1
HP:0002027  |  Abdominal pain  |  1
HP:0003613  |  Antiphospholipid antibodies  |  1
HP:0100653  |  Optic neuritis  |  1
HP:0002894  |  Neoplasia of the pancreas  |  1
HP:0002301  |  Hemiplegia  |  1
HP:0000716  |  Depression  |  1
HP:0000819  |  Diabetes mellitus  |  1
HP:0001878  |  Haemolytic anaemia  |  1
HP:0000969  |  Dropsy  |  1
HP:0100543  |  Cognitive deficits  |  1
HP:0000099  |  Glomerular nephritis  |  1
HP:0001677  |  Coronary artery disease  |  1
HP:0002664  |  Neoplasia  |  1
HP:0010702  |  Hypergammaglobulinaemia  |  1
HP:0000939  |  Osteoporosis  |  1
HP:0100512  |  Vitamin D deficiency  |  1
HP:0005550  |  Chronic lymphatic leukemia  |  1
HP:0001873  |  Low platelet count  |  1
HP:0003002  |  Breast carcinoma  |  1
HP:0001824  |  Weight loss  |  1
HP:0006824  |  Cranial nerve palsy  |  1
HP:0100778  |  Cryoglobulinemia  |  1
HP:0006775  |  Multiple myeloma  |  1
HP:0002090  |  Pneumonia  |  1
HP:0002721  |  Immunodeficiency  |  1
HP:0005523  |  Lymphoproliferative disorder  |  1
HP:0100633  |  Inflammation of the esophagus  |  1
HP:0003765  |  Psoriasis  |  1
HP:0004395  |  Malnutrition  |  1
HP:0000836  |  Overactive thyroid  |  1
HP:0011892  |  Vitamin K deficiency  |  1
HP:0010310  |  Chylothorax  |  1
HP:0012410  |  Pure red cell aplasia  |  1
HP:0001971  |  Hypersplenism  |  1
HP:0001511  |  Prenatal onset growth retardation  |  1
HP:0001909  |  Leukemia  |  1
HP:0002665  |  Lymphoma  |  1
HP:0001945  |  Fever  |  1
HP:0001289  |  Confusion  |  1
HP:0012531  |  Pain  |  1
HP:0001919  |  Acute renal failure  |  1
HP:0003774  |  End-stage renal failure  |  1
HP:0012486  |  Inflammation of spinal cord  |  1
HP:0000952  |  Yellow skin  |  1
HP:0012215  |  Testicular microlithiasis  |  1
Disease ID 1500
Disease viral hepatitis
Manually Symptom
UMLS  | Name(Total Manually Symptoms:94)
C2711227  |  hepatic steatosis
C2707258  |  infections
C2700513  |  aplastic anemia
C2364133  |  infection
C2364074  |  drug abuse
C2364072  |  depression
C2363741  |  hiv-1 infection
C2203646  |  jaundice
C2186532  |  liver disease
C2073625  |  pleural effusion
C2004456  |  postnecrotic cirrhosis
C1963165  |  malabsorption
C1963154  |  renal failure
C1963135  |  hepatic necrosis
C1963083  |  cholecystitis
C1962972  |  proteinuria
C1883018  |  severe aplastic anemia
C1623038  |  cirrhosis
C1611280  |  allergy
C1608426  |  compensated cirrhosis
C1512411  |  hepatocellular carcinoma
C1405749  |  hepatorenal syndrome
C1393529  |  vascular complications
C1387528  |  acute hemolytic anemia
C1000483  |  anemia
C0948906  |  bacterial allergy
C0936254  |  polyradiculoneuritis
C0919725  |  digital necrosis
C0877561  |  cholecystocholangitis
C0796095  |  c syndrome
C0542241  |  toxemia
C0442886  |  secondary infection
C0400929  |  subacute hepatic failure
C0259744  |  dysproteinemia
C0240805  |  prodrome
C0239946  |  liver fibrosis
C0239946  |  hepatic fibrosis
C0234935  |  acute urticaria
C0162557  |  fulminant hepatic failure
C0162557  |  acute liver failure
C0162557  |  acute hepatic failure
C0151798  |  liver necrosis
C0149678  |  ebv infection
C0085605  |  hepatic failure
C0040188  |  tic disorders
C0040149  |  subacute thyroiditis
C0040127  |  thyroid crisis
C0040034  |  thrombocytopenia
C0038826  |  superinfection
C0038395  |  streptococcal infection
C0038353  |  gastric dilatation
C0038160  |  staphylococcal infection
C0037284  |  skin lesions
C0037274  |  dermatologic disorders
C0036323  |  schistosomiasis
C0030326  |  panniculitis
C0030312  |  pancytopenia
C0027121  |  myositis
C0025010  |  measles
C0024537  |  tertian malaria
C0024141  |  systemic lupus erythematosus
C0023895  |  liver diseases
C0023890  |  liver cirrhosis
C0023890  |  hepatic cirrhosis
C0022660  |  acute kidney failure
C0022658  |  renal disease
C0022408  |  arthropathy
C0022408  |  arthropathies
C0021832  |  intestinal parasites
C0020437  |  hypercalcaemia
C0020433  |  bilirubinemia
C0019693  |  hiv infection
C0019212  |  hepato-renal syndrome
C0019151  |  hepatic encephalopathy
C0019151  |  coma hepaticum
C0019147  |  hepatic coma
C0019087  |  hemorrhagic diathesis
C0018799  |  heart disorders
C0018784  |  sensorineural hearing loss
C0015695  |  fatty liver
C0015469  |  facial paralysis
C0011860  |  diabetes
C0011849  |  diabetes mellitus
C0010403  |  cryoglobulinemia
C0010356  |  cross infection
C0008372  |  intrahepatic cholestasis
C0008370  |  cholestasis
C0006840  |  candidiasis
C0006111  |  brain disorders
C0005416  |  biliary dyskinesia
C0003864  |  arthritis
C0002881  |  congenital hemolytic anemia
C0002879  |  acquired hemolytic anemia
C0001339  |  acute pancreatitis
Text Mined Symptom
UMLS | Name | Sentences' Count(Total Symptoms:28)
C0023890  |  cirrhosis  |  22
C0023895  |  liver disease  |  19
C0009450  |  infection  |  17
C0239946  |  liver fibrosis  |  16
C0019204  |  hepatocellular carcinoma  |  8
C0085605  |  hepatic failure  |  3
C0001339  |  acute pancreatitis  |  3
C0162557  |  acute liver failure  |  3
C0008325  |  cholecystitis  |  3
C0162557  |  fulminant hepatic failure  |  3
C0002871  |  anemia  |  3
C0021311  |  infections  |  2
C0002874  |  aplastic anemia  |  2
C0023890  |  liver cirrhosis  |  2
C0008370  |  cholestasis  |  2
C0796095  |  c syndrome  |  2
C0239946  |  hepatic fibrosis  |  2
C0023895  |  liver diseases  |  1
C0011849  |  diabetes mellitus  |  1
C0015695  |  fatty liver  |  1
C0022346  |  jaundice  |  1
C0010403  |  cryoglobulinemia  |  1
C0011847  |  diabetes  |  1
C0022658  |  renal disease  |  1
C0036323  |  schistosomiasis  |  1
C0040034  |  thrombocytopenia  |  1
C0038826  |  superinfection  |  1
C0011570  |  depression  |  1
Manually Genotype(Total Text Mining Genotypes:0)
(Waiting for update.)
Text Mining Genotype(Total 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
rs25487240184917515XRCC1umls:C0042721BeFreeThe XRCC1 rs25487 polymorphism may influence the development of cirrhosis in viral hepatitis patients, and additional investigation will be necessary.0.0005428842014XRCC11943551574TC
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.)
Disease ID 1500
Disease viral hepatitis
Case(Waiting for update.)