PedAM

Pediatric Disease Annotations & Medicines


	hepatitis e

Disease ID	759
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	DOID:4411
UMLS	C0085293
MeSH	D016751
SNOMED-CT	SNOMEDCT_US_2016_09_01:7111000119109
Comorbidity	UMLS \| Disease \| Sentences' Count(Total Sentences:44) C0019158 \| hepatitis \| 11 C0018378 \| guillain-barre syndrome \| 9 C0042721 \| viral hepatitis \| 5 C0019163 \| hepatitis b \| 4 C0023418 \| leukemia \| 3 C0241910 \| autoimmune hepatitis \| 3 C0030305 \| pancreatitis \| 3 C0001339 \| acute pancreatitis \| 3 C0035078 \| renal failure \| 2 C0023890 \| cirrhosis \| 2 C0022660 \| acute renal failure \| 2 C0011226 \| hepatitis d \| 2 C0023364 \| leptospirosis \| 1 C0026986 \| myelodysplastic syndromes \| 1 C0376175 \| bell's palsy \| 1 C0026896 \| myasthenia gravis \| 1 C0003873 \| rheumatoid arthritis \| 1 C0024299 \| lymphoma \| 1 C0026986 \| myelodysplastic syndrome \| 1 C0005283 \| beta thalassemia \| 1 C0019151 \| hepatic encephalopathy \| 1 C0002871 \| anaemia \| 1 C0023449 \| acute lymphoblastic leukemia \| 1 C0040188 \| tic disorders \| 1 C0442874 \| neuropathy \| 1 C0040034 \| thrombocytopenia \| 1 C0002878 \| haemolytic anaemia \| 1 C0023890 \| liver cirrhosis \| 1 C0376545 \| hematological malignancies \| 1 C0032587 \| polyradiculoneuropathy \| 1 C0036323 \| schistosomiasis \| 1 C0003864 \| arthritis \| 1 C0003864 \| arthritides \| 1 C0920350 \| autoimmune thyroiditis \| 1 C0024141 \| systemic lupus erythematosus \| 1 C0023895 \| liver disease \| 1 C0023448 \| lymphoblastic leukemia \| 1 C0409974 \| lupus erythematosus \| 1 C0022658 \| renal disease \| 1 C0079731 \| b cell lymphoma \| 1 C0023895 \| hepatic disorders \| 1 C0019187 \| alcoholic hepatitis \| 1 C0025637 \| methemoglobinemia \| 1 C0017920 \| g6pd deficiency \| 1
Curated Gene	(Waiting for update.)
Inferring Gene	Entrez_id \| Symbol \| Resource(Total Genes:1) 3458 \| IFNG \| infer
Text Mined Gene	Entrez_id \| Symbol \| Score \| Resource(Total Genes:100) 80341 \| BPIFB2 \| DISEASES 51311 \| TLR8 \| DISEASES 27344 \| PCSK1N \| DISEASES 973 \| CD79A \| DISEASES 2077 \| ERF \| DISEASES 969 \| CD69 \| DISEASES 5754 \| PTK7 \| DISEASES 718 \| C3 \| DISEASES 2678 \| GGT1 \| DISEASES 7251 \| TSG101 \| DISEASES 6155 \| RPL27 \| DISEASES 27183 \| VPS4A \| DISEASES 129607 \| CMPK2 \| DISEASES 9043 \| SPAG9 \| DISEASES 22858 \| ICK \| DISEASES 3682 \| ITGAE \| DISEASES 8190 \| MIA \| DISEASES 51430 \| SUCO \| DISEASES 7879 \| RAB7A \| DISEASES 10058 \| ABCB6 \| DISEASES 27125 \| AFF4 \| DISEASES 3756 \| KCNH1 \| DISEASES 5868 \| RAB5A \| DISEASES 925 \| CD8A \| DISEASES 136991 \| ASZ1 \| DISEASES 8883 \| NAE1 \| DISEASES 9437 \| NCR1 \| DISEASES 3046 \| HBE1 \| DISEASES 1973 \| EIF4A1 \| DISEASES 6051 \| RNPEP \| DISEASES 213 \| ALB \| DISEASES 7098 \| TLR3 \| DISEASES 6447 \| SCG5 \| DISEASES 51435 \| SCARA3 \| DISEASES 140738 \| TMEM37 \| DISEASES 1493 \| CTLA4 \| DISEASES 7399 \| USH2A \| DISEASES 2244 \| FGB \| DISEASES 2243 \| FGA \| DISEASES 3669 \| ISG20 \| DISEASES 160065 \| PATE1 \| DISEASES 2147 \| F2 \| DISEASES 3661 \| IRF3 \| DISEASES 22949 \| PTGR1 \| DISEASES 11322 \| TMC6 \| DISEASES 6773 \| STAT2 \| DISEASES 653423 \| SPAG11A \| DISEASES 53347 \| UBASH3A \| DISEASES 83787 \| ARMC10 \| DISEASES 23019 \| CNOT1 \| DISEASES 10611 \| PDLIM5 \| DISEASES 56252 \| YLPM1 \| DISEASES 1974 \| EIF4A2 \| DISEASES 400668 \| PRSS57 \| DISEASES 23467 \| NPTXR \| DISEASES 5034 \| P4HB \| DISEASES 8784 \| TNFRSF18 \| DISEASES 9074 \| CLDN6 \| DISEASES 3665 \| IRF7 \| DISEASES 10732 \| TCFL5 \| DISEASES 2266 \| FGG \| DISEASES 1981 \| EIF4G1 \| DISEASES 259197 \| NCR3 \| DISEASES 3716 \| JAK1 \| DISEASES 6218 \| RPS17 \| DISEASES 51530 \| ZC3HC1 \| DISEASES 4149 \| MAX \| DISEASES 1066 \| CES1 \| DISEASES 916 \| CD3E \| DISEASES 4514 \| MT-CO3 \| DISEASES 5455 \| POU3F3 \| DISEASES 1660 \| DHX9 \| DISEASES 26002 \| MOXD1 \| DISEASES 7062 \| TCHH \| DISEASES 959 \| CD40LG \| DISEASES 8569 \| MKNK1 \| DISEASES 9436 \| NCR2 \| DISEASES 316 \| AOX1 \| DISEASES 50943 \| FOXP3 \| DISEASES 7091 \| TLE4 \| DISEASES 22894 \| DIS3 \| DISEASES 3030 \| HADHA \| DISEASES 51284 \| TLR7 \| DISEASES 158326 \| FREM1 \| DISEASES 6710 \| SPTB \| DISEASES 10379 \| IRF9 \| DISEASES 10407 \| SPAG11B \| DISEASES 728441 \| GGT2 \| DISEASES 25983 \| NGDN \| DISEASES 124997 \| WDR81 \| DISEASES 7124 \| TNF \| DISEASES 4615 \| MYD88 \| DISEASES 3586 \| IL10 \| DISEASES 127933 \| UHMK1 \| DISEASES 2053 \| EPHX2 \| DISEASES 4168 \| MCF2 \| DISEASES 10846 \| PDE10A \| DISEASES 22861 \| NLRP1 \| DISEASES 284424 \| MIR7-3HG \| DISEASES 246734 \| NPCDR1 \| DISEASES
Locus	(Waiting for update.)

Disease ID	759
Disease	hepatitis e
Integrated Phenotype	(Waiting for update.)
Text Mined Phenotype	HPO \| Name \| Sentences' Count(Total Phenotypes:37) HP:0012115 \| Liver inflammation \| 11 HP:0001399 \| Liver failure \| 10 HP:0200119 \| Acute liver inflammation \| 8 HP:0006554 \| Acute hepatic failure \| 5 HP:0006562 \| Viral hepatitis \| 5 HP:0001919 \| Acute renal failure \| 3 HP:0200123 \| Chronic liver inflammation \| 3 HP:0000952 \| Yellow skin \| 3 HP:0001909 \| Leukemia \| 3 HP:0001735 \| Acute pancreatitis \| 2 HP:0001733 \| Pancreatic inflammation \| 2 HP:0001394 \| Hepatic cirrhosis \| 2 HP:0000083 \| Renal insufficiency \| 2 HP:0012119 \| Methemoglobinemia \| 1 HP:0002721 \| Immunodeficiency \| 1 HP:0001369 \| Arthritis \| 1 HP:0010628 \| Facial palsy, unilateral or bilateral \| 1 HP:0004787 \| Fulminant hepatitis \| 1 HP:0002725 \| Systemic lupus erythematosus \| 1 HP:0001903 \| Anemia \| 1 HP:0001878 \| Haemolytic anaemia \| 1 HP:0100626 \| Chronic hepatic failure \| 1 HP:0003473 \| Fatigable weakness \| 1 HP:0001873 \| Low platelet count \| 1 HP:0100033 \| Tic disorder \| 1 HP:0003202 \| Neurogenic muscle atrophy, especially in the lower limbs \| 1 HP:0001370 \| Rheumatoid arthritis \| 1 HP:0001324 \| Muscular weakness \| 1 HP:0012191 \| B-cell lymphoma \| 1 HP:0012531 \| Pain \| 1 HP:0002863 \| Myelodysplastic syndrome \| 1 HP:0002910 \| Elevated transaminases \| 1 HP:0002665 \| Lymphoma \| 1 HP:0004448 \| Fulminant hepatic failure \| 1 HP:0001298 \| Encephalopathy \| 1 HP:0006721 \| Acute lymphocytic leukemia \| 1 HP:0002480 \| Hepatic encephalopathy \| 1

Disease ID	759
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 \| 13 C0267797 \| acute hepatitis \| 8 C0276622 \| acute viral hepatitis \| 3 C0030305 \| pancreatitis \| 2 C0022660 \| acute renal failure \| 2 C0854537 \| zoonotic infection \| 2 C0275518 \| acute infection \| 1 C0162557 \| fulminant hepatic failure \| 1 C0038826 \| superinfection \| 1 C0042749 \| viremia \| 1

Manually Genotype(Total Text Mining 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.)

Chemical(Total Drugs:0)
(Waiting for update.)

FDA approved drug and dosage information(Total Drugs:0)
(Waiting for update.)

FDA labeling changes(Total Drugs:0)
(Waiting for update.)

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