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eRAM

encyclopedia of Rare Disease Annotation for Precision Medicine



   hepatitis e
  

Disease ID 1295
Disease hepatitis e
Definition
Acute INFLAMMATION of the LIVER in humans; caused by HEPATITIS E VIRUS, a non-enveloped single-stranded RNA virus. Similar to HEPATITIS A, its incubation period is 15-60 days and is enterically transmitted, usually by fecal-oral transmission.
Synonym
e hepatitis
enterically transmitted non a, non b hepatitis
enterically-transmitted non-a, non-b hepatitis
epidemic non a, non b hepatitis
epidemic non-a, non-b hepatitis
et nanbh
et-nanbh
hepatitides, water-borne
hepatitis e [disease/finding]
hepatitis e virus infection
hepatitis, viral, non-a, non-b, enterically-transmitted
hepatitis, water borne
hepatitis, water-borne
viral hepatitis e
viral hepatitis type e
viral hepatitis type e (disorder)
water-borne hepatitides
water-borne hepatitis
DOID
UMLS
C0085293
MeSH
SNOMED-CT
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:184)
C0019158  |  hepatitis  |  35
C0023890  |  cirrhosis  |  21
C0019163  |  hepatitis b  |  18
C0019204  |  hepatocellular carcinoma  |  13
C0023895  |  liver disease  |  11
C0042769  |  virus infection  |  10
C0018378  |  guillain-barre syndrome  |  9
C0023890  |  liver cirrhosis  |  8
C0085293  |  hepatitis e  |  7
C0008370  |  cholestasis  |  6
C0008311  |  cholangitis  |  6
C0085253  |  adult-onset still's disease  |  6
C0008312  |  primary biliary cirrhosis  |  5
C0001339  |  acute pancreatitis  |  5
C0030305  |  pancreatitis  |  5
C0003873  |  rheumatoid arthritis  |  5
C0042721  |  viral hepatitis  |  5
C0040034  |  thrombocytopenia  |  5
C0008312  |  biliary cirrhosis  |  5
C0026769  |  multiple sclerosis  |  4
C0007570  |  celiac disease  |  4
C0002871  |  anaemia  |  4
C0003864  |  arthritis  |  4
C0021053  |  immune disease  |  4
C0023418  |  leukemia  |  4
C0009319  |  colitis  |  3
C0040147  |  thyroiditis  |  3
C0034362  |  q fever  |  3
C0042769  |  viral infection  |  3
C0024299  |  lymphoma  |  3
C0019196  |  hepatitis c  |  3
C0022354  |  cholestatic jaundice  |  3
C0152025  |  polyneuropathy  |  3
C0241910  |  autoimmune hepatitis  |  3
C0281963  |  red cell aplasia  |  3
C0020538  |  hypertension  |  3
C0019187  |  alcoholic hepatitis  |  2
C0002878  |  hemolytic anemia  |  2
C0442874  |  neuropathy  |  2
C0030312  |  pancytopenia  |  2
C0005283  |  beta thalassemia  |  2
C0021390  |  inflammatory bowel disease  |  2
C0023895  |  hepatic disorders  |  2
C0085253  |  adult-onset still disease  |  2
C0002871  |  anemia  |  2
C0026896  |  myasthenia gravis  |  2
C0008313  |  sclerosing cholangitis  |  2
C0031036  |  polyarteritis nodosa  |  2
C0409974  |  lupus erythematosus  |  2
C0002880  |  autoimmune hemolytic anemia  |  2
C0018801  |  heart failure  |  2
C0040188  |  tic disorders  |  2
C0026946  |  fungal infection  |  2
C0022660  |  acute renal failure  |  2
C0031154  |  peritonitis  |  2
C0040149  |  subacute thyroiditis  |  2
C0021831  |  bowel disease  |  2
C0024141  |  systemic lupus erythematosus  |  2
C0009324  |  ulcerative colitis  |  2
C0035078  |  renal failure  |  2
C0085655  |  polymyositis  |  2
C0018213  |  graves' disease  |  2
C0023903  |  liver cancer  |  2
C0020541  |  portal hypertension  |  2
C0003467  |  anxiety  |  2
C0036421  |  systemic sclerosis  |  2
C0376175  |  bell's palsy  |  2
C0011847  |  diabetes  |  2
C0002878  |  haemolytic anaemia  |  2
C0040100  |  thymoma  |  2
C0017665  |  membranous glomerulonephritis  |  2
C0034902  |  pure red cell aplasia  |  2
C0920350  |  autoimmune thyroiditis  |  2
C0566602  |  primary sclerosing cholangitis  |  2
C0017658  |  glomerulonephritis  |  2
C0085253  |  adult onset still's disease  |  2
C0020455  |  hypergammaglobulinaemia  |  1
C0010414  |  cryptococcosis  |  1
C0025309  |  meningoencephalitis  |  1
C0008372  |  intrahepatic cholestasis  |  1
C0019147  |  hepatic coma  |  1
C0042721  |  virus hepatitis  |  1
C0023449  |  acute lymphoblastic leukemia  |  1
C0023903  |  hepatic cancer  |  1
C0679466  |  cognitive deficits  |  1
C0701818  |  choledocholithiasis  |  1
C0393819  |  chronic inflammatory demyelinating polyneuropathy  |  1
C0554114  |  epstein-barr virus hepatitis  |  1
C0037061  |  siderosis  |  1
C0025289  |  meningitis  |  1
C0027059  |  myocarditis  |  1
C0026986  |  myelodysplastic syndromes  |  1
C0011991  |  diarrhea  |  1
C0836924  |  thrombocytosis  |  1
C0004712  |  balo's concentric sclerosis  |  1
C0677607  |  hashimoto's thyroiditis  |  1
C0019202  |  wilson's disease  |  1
C0023646  |  lichen planus  |  1
C0033860  |  psoriasis  |  1
C0019151  |  hepatic encephalopathy  |  1
C0023890  |  hepatic cirrhosis  |  1
C0011226  |  hepatitis d  |  1
C0036323  |  schistosomiasis  |  1
C0002726  |  amyloidosis  |  1
C0023895  |  hepatopathy  |  1
C0024291  |  hemophagocytic lymphohistiocytosis  |  1
C0019360  |  zoster  |  1
C0270922  |  demyelinating polyneuropathy  |  1
C0023470  |  myelocytic leukemia  |  1
C1527336  |  sjogren's syndrome  |  1
C0162429  |  poor nutrition  |  1
C0015930  |  fetal distress  |  1
C0018203  |  chronic granulomatous disease  |  1
C0039128  |  syphilis  |  1
C0040128  |  thyroid disease  |  1
C0002880  |  autoimmune haemolytic anaemia  |  1
C0025293  |  listeria monocytogenes meningitis  |  1
C0085652  |  pyoderma gangrenosum  |  1
C2700641  |  lymphoplasmacytic lymphoma  |  1
C0272286  |  immune thrombocytopenia  |  1
C0022658  |  kidney disease  |  1
C0011854  |  type 1 diabetes mellitus  |  1
C0009782  |  connective tissue disease  |  1
C0039730  |  thalassemia  |  1
C0023487  |  promyelocytic leukemia  |  1
C0002874  |  aplastic anaemia  |  1
C0024314  |  lymphoproliferative disorder  |  1
C0023903  |  hepatic tumor  |  1
C0023470  |  myeloid leukemia  |  1
C0022661  |  chronic kidney disease  |  1
C0023787  |  lipodystrophy  |  1
C0019829  |  hodgkin's lymphoma  |  1
C1619734  |  pulmonary arterial hypertension  |  1
C0026986  |  myelodysplastic syndrome  |  1
C0023290  |  visceral leishmaniasis  |  1
C0151313  |  sensory neuropathy  |  1
C0085273  |  erythema infectiosum  |  1
C0011633  |  dermatomyositis  |  1
C0002874  |  aplastic anemia  |  1
C0003125  |  anorexia nervosa  |  1
C0376545  |  hematological malignancies  |  1
C0019163  |  hepatitis b infection  |  1
C0032587  |  polyradiculoneuropathy  |  1
C0008049  |  varicella  |  1
C0023801  |  lipomatosis  |  1
C0685938  |  gastrointestinal cancer  |  1
C0035309  |  retinopathy  |  1
C0162529  |  ischemic colitis  |  1
C0494491  |  mononeuropathy  |  1
C0002892  |  pernicious anemia  |  1
C0003864  |  arthritides  |  1
C0023281  |  leishmaniasis  |  1
C0221032  |  generalized lipodystrophy  |  1
C0011849  |  diabetes mellitus  |  1
C0022658  |  renal disease  |  1
C0023343  |  leprosy  |  1
C0012739  |  disseminated intravascular coagulation  |  1
C0268397  |  cutaneous amyloidosis  |  1
C0008325  |  cholecystitis  |  1
C0040128  |  thyroid diseases  |  1
C0009447  |  common variable immunodeficiency  |  1
C0030312  |  bone marrow failure  |  1
C0023364  |  leptospirosis  |  1
C0013371  |  shigellosis  |  1
C0026272  |  mixed connective tissue disease  |  1
C0023448  |  lymphoblastic leukemia  |  1
C0017920  |  g6pd deficiency  |  1
C0025637  |  methemoglobinemia  |  1
C0012739  |  disseminated intravascular coagulation (dic)  |  1
C0011570  |  depression  |  1
C0040127  |  thyroid storm  |  1
C0019212  |  hepatorenal syndrome  |  1
C0001206  |  acromegaly  |  1
C0023467  |  acute myeloid leukemia  |  1
C0006309  |  brucellosis  |  1
C0267841  |  acalculous cholecystitis  |  1
C0023487  |  acute promyelocytic leukemia  |  1
C0014038  |  encephalitis  |  1
C0034212  |  pyoderma  |  1
C0042164  |  uveitis  |  1
C0079731  |  b cell lymphoma  |  1
C0024314  |  lymphoproliferative disorders  |  1
C0027947  |  neutropenia  |  1
C0011854  |  type 1 diabetes  |  1
Curated Gene(Waiting for update.)
Inferring Gene
Entrez_id | Symbol | Resource(Total Genes:1)
3458  |  IFNG  |  CIPHER
Text Mined Gene
Entrez_id | Symbol | Score | Resource(Total Genes:51)
316  |  AOX1  |  1.873  |  DISEASES
916  |  CD3E  |  1.831  |  DISEASES
959  |  CD40LG  |  6.071  |  DISEASES
1066  |  CES1  |  1.335  |  DISEASES
9074  |  CLDN6  |  2.063  |  DISEASES
23019  |  CNOT1  |  2.248  |  DISEASES
1660  |  DHX9  |  1.348  |  DISEASES
22894  |  DIS3  |  2.324  |  DISEASES
1974  |  EIF4A2  |  1.879  |  DISEASES
1981  |  EIF4G1  |  1.406  |  DISEASES
2053  |  EPHX2  |  1.411  |  DISEASES
2266  |  FGG  |  1.806  |  DISEASES
50943  |  FOXP3  |  1.258  |  DISEASES
158326  |  FREM1  |  2.258  |  DISEASES
728441  |  GGT2  |  1.506  |  DISEASES
3030  |  HADHA  |  3.765  |  DISEASES
3586  |  IL10  |  1.423  |  DISEASES
3665  |  IRF7  |  1.095  |  DISEASES
10379  |  IRF9  |  1.835  |  DISEASES
3716  |  JAK1  |  1.376  |  DISEASES
4149  |  MAX  |  2.141  |  DISEASES
4168  |  MCF2  |  1.516  |  DISEASES
284424  |  MIR7-3HG  |  2.507  |  DISEASES
8569  |  MKNK1  |  2.072  |  DISEASES
26002  |  MOXD1  |  1.799  |  DISEASES
4514  |  MT-CO3  |  1.12  |  DISEASES
4615  |  MYD88  |  1.057  |  DISEASES
9436  |  NCR2  |  1.588  |  DISEASES
259197  |  NCR3  |  1.244  |  DISEASES
25983  |  NGDN  |  1.723  |  DISEASES
22861  |  NLRP1  |  1.353  |  DISEASES
246734  |  NPCDR1  |  4.697  |  DISEASES
23467  |  NPTXR  |  1.623  |  DISEASES
5034  |  P4HB  |  1.306  |  DISEASES
10846  |  PDE10A  |  1.51  |  DISEASES
10611  |  PDLIM5  |  1.533  |  DISEASES
5455  |  POU3F3  |  1.881  |  DISEASES
400668  |  PRSS57  |  1.945  |  DISEASES
6218  |  RPS17  |  2.179  |  DISEASES
10407  |  SPAG11B  |  3.56  |  DISEASES
6710  |  SPTB  |  1.632  |  DISEASES
10732  |  TCFL5  |  1.429  |  DISEASES
7062  |  TCHH  |  1.312  |  DISEASES
7091  |  TLE4  |  2.234  |  DISEASES
51284  |  TLR7  |  1.336  |  DISEASES
7124  |  TNF  |  1.032  |  DISEASES
8784  |  TNFRSF18  |  2.627  |  DISEASES
127933  |  UHMK1  |  1.687  |  DISEASES
124997  |  WDR81  |  2.93  |  DISEASES
56252  |  YLPM1  |  3.794  |  DISEASES
51530  |  ZC3HC1  |  2.557  |  DISEASES
Locus(Waiting for update.)
Disease ID 1295
Disease hepatitis e
Integrated Phenotype(Waiting for update.)
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:121)
HP:0012115  |  Liver inflammation  |  39
HP:0001399  |  Liver failure  |  32
HP:0200123  |  Chronic liver inflammation  |  21
HP:0001394  |  Hepatic cirrhosis  |  21
HP:0000952  |  Yellow skin  |  14
HP:0001402  |  Hepatocellular carcinoma  |  13
HP:0030731  |  Carcinoma  |  12
HP:0006554  |  Acute hepatic failure  |  10
HP:0200119  |  Acute liver inflammation  |  10
HP:0004448  |  Fulminant hepatic failure  |  7
HP:0001396  |  Cholestasis  |  7
HP:0001919  |  Acute renal failure  |  7
HP:0001370  |  Rheumatoid arthritis  |  6
HP:0004787  |  Fulminant hepatitis  |  6
HP:0001945  |  Fever  |  6
HP:0030151  |  Cholangitis  |  6
HP:0001903  |  Anemia  |  6
HP:0001369  |  Arthritis  |  5
HP:0002608  |  Celiac disease  |  5
HP:0002910  |  Elevated transaminases  |  5
HP:0006562  |  Viral hepatitis  |  5
HP:0002613  |  Biliary cirrhosis  |  5
HP:0001873  |  Low platelet count  |  4
HP:0001909  |  Leukemia  |  4
HP:0001878  |  Haemolytic anaemia  |  4
HP:0001733  |  Pancreatic inflammation  |  4
HP:0002960  |  Autoimmune condition  |  4
HP:0001735  |  Acute pancreatitis  |  4
HP:0001271  |  Polyneuropathy  |  3
HP:0100646  |  Thyroiditis  |  3
HP:0012410  |  Pure red cell aplasia  |  3
HP:0001890  |  Autoimmune hemolytic anemia  |  3
HP:0002665  |  Lymphoma  |  3
HP:0002583  |  Colitis  |  3
HP:0000822  |  Hypertension  |  3
HP:0001397  |  Hepatic steatosis  |  3
HP:0012531  |  Pain  |  3
HP:0001395  |  Hepatic fibrosis  |  3
HP:0100033  |  Tic disorder  |  2
HP:0012578  |  Membranous glomerulonephritis  |  2
HP:0012378  |  Fatigue  |  2
HP:0100279  |  Ulcerative colitis  |  2
HP:0001409  |  Portal hypertension  |  2
HP:0002721  |  Immunodeficiency  |  2
HP:0000819  |  Diabetes mellitus  |  2
HP:0001635  |  Congestive heart failure  |  2
HP:0010628  |  Facial palsy, unilateral or bilateral  |  2
HP:0000099  |  Glomerular nephritis  |  2
HP:0001259  |  Coma  |  2
HP:0000739  |  Anxiety  |  2
HP:0001876  |  Low blood cell count  |  2
HP:0002896  |  Liver cancer  |  2
HP:0003493  |  Elevated antinuclear antibody  |  2
HP:0002725  |  Systemic lupus erythematosus  |  2
HP:0010783  |  Erythema  |  2
HP:0100522  |  Thymoma  |  2
HP:0000083  |  Renal insufficiency  |  2
HP:0003473  |  Fatigable weakness  |  2
HP:0001414  |  Microvesicular hepatic steatosis  |  2
HP:0002586  |  Peritonitis  |  2
HP:0002664  |  Neoplasia  |  2
HP:0012119  |  Methemoglobinemia  |  1
HP:0000845  |  Acromegalic growth  |  1
HP:0003256  |  Coagulopathy  |  1
HP:0001915  |  Aplastic anemia  |  1
HP:0005523  |  Lymphoproliferative disorder  |  1
HP:0006580  |  Portal fibrosis  |  1
HP:0002863  |  Myelodysplastic syndrome  |  1
HP:0006573  |  Acute fatty liver  |  1
HP:0001406  |  Intrahepatic cholestasis  |  1
HP:0000999  |  Pyoderma  |  1
HP:0003613  |  Antiphospholipid antibodies  |  1
HP:0009125  |  Lipodystrophy  |  1
HP:0001082  |  Cholecystitis  |  1
HP:0012324  |  Myeloid leukemia  |  1
HP:0100626  |  Chronic hepatic failure  |  1
HP:0009064  |  Generalized lipodystrophy  |  1
HP:0001880  |  Eosinophilia  |  1
HP:0002202  |  Pleural effusion  |  1
HP:0012819  |  Myocarditis  |  1
HP:0001404  |  Hepatocellular necrosis  |  1
HP:0005528  |  Bone marrow hypoplasia  |  1
HP:0012309  |  Cutaneous amyloidosis  |  1
HP:0002480  |  Hepatic encephalopathy  |  1
HP:0200042  |  Skin ulcer  |  1
HP:0100543  |  Cognitive deficits  |  1
HP:0100754  |  Mania  |  1
HP:0001904  |  Autoimmune neutropenia  |  1
HP:0001298  |  Encephalopathy  |  1
HP:0000488  |  Noninflammatory retina disease  |  1
HP:0001894  |  Thrombocytosis  |  1
HP:0006721  |  Acute lymphocytic leukemia  |  1
HP:0012189  |  Hodgkin disease  |  1
HP:0000716  |  Depression  |  1
HP:0000763  |  Sensory neuropathy  |  1
HP:0002383  |  Encephalitis  |  1
HP:0004836  |  Acute promyelocytic leukemia  |  1
HP:0030717  |  Meconium peritonitis  |  1
HP:0000872  |  Hashimoto's thyroiditis  |  1
HP:0012622  |  Chronic kidney disease  |  1
HP:0010702  |  Hypergammaglobulinaemia  |  1
HP:0001287  |  Meningitis  |  1
HP:0012191  |  B-cell lymphoma  |  1
HP:0001973  |  Autoimmune thrombocytopenia  |  1
HP:0100806  |  Sepsis  |  1
HP:0009831  |  Single damaged nerve  |  1
HP:0004808  |  Acute myelogenous leukemia  |  1
HP:0007178  |  Motor polyneuropathy  |  1
HP:0011034  |  Amyloid disease  |  1
HP:0002273  |  Tetraparesis  |  1
HP:0002018  |  Nausea  |  1
HP:0002039  |  Anorexia  |  1
HP:0003765  |  Psoriasis  |  1
HP:0001875  |  Neutropenia  |  1
HP:0002014  |  Diarrhea  |  1
HP:0100665  |  Angiooedema  |  1
HP:0005521  |  Disseminated intravascular coagulation  |  1
HP:0003202  |  Neurogenic muscle atrophy, especially in the lower limbs  |  1
HP:0000820  |  Thyroid abnormality  |  1
HP:0001324  |  Muscular weakness  |  1
HP:0000554  |  Uveitis  |  1
Disease ID 1295
Disease hepatitis e
Manually Symptom
UMLS  | Name(Total Manually Symptoms:20)
C2707258  |  infections
C2364133  |  infection
C1963198  |  pancreatitis
C1510479  |  neuralgic amyotrophy
C1264606  |  persistent infection
C0854537  |  zoonotic infection
C0542035  |  erythroid hypoplasia
C0400929  |  subacute hepatic failure
C0276622  |  acute viral hepatitis
C0275522  |  subclinical infection
C0275518  |  acute infection
C0272286  |  immune thrombocytopenia
C0267797  |  acute hepatitis
C0162557  |  fulminant hepatic failure
C0042749  |  viremia
C0038826  |  superinfection
C0027613  |  giant cell hepatitis
C0022660  |  acute renal failure
C0008370  |  cholestasis
C0007222  |  cardiovascular disorders
Text Mined Symptom
UMLS | Name | Sentences' Count(Total Symptoms:11)
C0009450  |  infection  |  37
C0021311  |  infections  |  12
C0267797  |  acute hepatitis  |  8
C0276622  |  acute viral hepatitis  |  3
C0854537  |  zoonotic infection  |  2
C0022660  |  acute renal failure  |  2
C0038826  |  superinfection  |  1
C0030305  |  pancreatitis  |  1
C0162557  |  fulminant hepatic failure  |  1
C0042749  |  viremia  |  1
C0275518  |  acute infection  |  1
Manually Genotype(Total Text Mining Genotypes:0)
(Waiting for update.)
Text Mining Genotype(Total Genotypes:0)
(Waiting for update.)
All Snps(Total Genotypes:0)
(Waiting for update.)
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 1295
Disease hepatitis e
Case(Waiting for update.)