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Pediatric Disease Annotations & Medicines



   dengue hemorrhagic fever
  

Disease ID 805
Disease dengue hemorrhagic fever
Definition
A virulent form of dengue characterized by THROMBOCYTOPENIA and an increase in vascular permeability (grades I and II) and distinguished by a positive pain test (e.g., TOURNIQUET PAIN TEST). When accompanied by SHOCK (grades III and IV), it is called dengue shock syndrome.
Synonym
dengue fever haemorrhagic
dengue fever hemorrhagic
dengue haemorrhagic fever
dengue haemorrhagic fever (disorder)
dengue hemorrhagic
dengue hemorrhagic fever (disorder)
dengue, severe
dengues, severe
dhf - dengue haemorrhagic fever
dhf - dengue hemorrhagic fever
double dengue hemorrhagic disease
fever, philippine hemorrhagic
fever, singapore hemorrhagic
fever, thai hemorrhagic
haemorrhagic dengue fever
hemorrhagic dengue
hemorrhagic dengue fever
hemorrhagic dengues
hemorrhagic fever, dengue
philippine hemorrhagic fever
severe dengue
severe dengue [disease/finding]
severe dengues
singapore hemorrhagic fever
thai hemorrhagic fever
DOID
ICD10
UMLS
C0019100
MeSH
SNOMED-CT
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:21)
C0040034  |  thrombocytopenia  |  5
C0030305  |  pancreatitis  |  3
C0376300  |  dengue shock syndrome  |  3
C0001339  |  acute pancreatitis  |  3
C0032001  |  pituitary apoplexy  |  2
C0002871  |  anemia  |  1
C0035222  |  acute respiratory distress syndrome  |  1
C0343084  |  capillary leak syndrome  |  1
C0155686  |  acute myocarditis  |  1
C0043395  |  yellow fever  |  1
C0024530  |  malaria  |  1
C0267211  |  watermelon stomach  |  1
C0008325  |  cholecystitis  |  1
C0001824  |  agranulocytosis  |  1
C0024291  |  hemophagocytic lymphohistiocytosis  |  1
C0267841  |  acalculous cholecystitis  |  1
C0032000  |  pituitary adenoma  |  1
C0042769  |  virus infection  |  1
C1704437  |  respiratory distress syndrome  |  1
C0027059  |  myocarditis  |  1
C0011880  |  diabetic ketoacidosis  |  1
Curated Gene
Entrez_id | Symbol | Resource(Total Genes:3)
MICB  |  4277  |  CTD_human
PLCE1  |  51196  |  CTD_human
CLEC5A  |  23601  |  CTD_human
Inferring Gene
Entrez_id | Symbol | Resource(Total Genes:102)
103  |  ADAR  |  infer
9716  |  AQR  |  infer
367  |  AR  |  infer
30835  |  CD209  |  infer
975  |  CD81  |  infer
3075  |  CFH  |  infer
1158  |  CKM  |  infer
170482  |  CLEC4C  |  infer
1387  |  CREBBP  |  infer
1588  |  CYP19A1  |  infer
1576  |  CYP3A4  |  infer
1813  |  DRD2  |  infer
30008  |  EFEMP2  |  infer
5610  |  EIF2AK2  |  infer
2165  |  F13B  |  infer
8772  |  FADD  |  infer
2212  |  FCGR2A  |  infer
2213  |  FCGR2B  |  infer
2638  |  GC  |  infer
2784  |  GNB3  |  infer
3000  |  GUCY2D  |  infer
3123  |  HLA-DRB1  |  infer
3383  |  ICAM1  |  infer
3439  |  IFNA1  |  infer
3446  |  IFNA10  |  infer
3447  |  IFNA13  |  infer
3448  |  IFNA14  |  infer
3449  |  IFNA16  |  infer
3451  |  IFNA17  |  infer
3440  |  IFNA2  |  infer
3452  |  IFNA21  |  infer
3441  |  IFNA4  |  infer
3442  |  IFNA5  |  infer
3443  |  IFNA6  |  infer
3445  |  IFNA8  |  infer
3454  |  IFNAR1  |  infer
3455  |  IFNAR2  |  infer
3456  |  IFNB1  |  infer
338376  |  IFNE  |  infer
3458  |  IFNG  |  infer
3459  |  IFNGR1  |  infer
3460  |  IFNGR2  |  infer
56832  |  IFNK  |  infer
3467  |  IFNW1  |  infer
9641  |  IKBKE  |  infer
3586  |  IL10  |  infer
3587  |  IL10RA  |  infer
3554  |  IL1R1  |  infer
7850  |  IL1R2  |  infer
3565  |  IL4  |  infer
3569  |  IL6  |  infer
51135  |  IRAK4  |  infer
3659  |  IRF1  |  infer
3663  |  IRF5  |  infer
3665  |  IRF7  |  infer
3682  |  ITGAE  |  infer
3690  |  ITGB3  |  infer
3716  |  JAK1  |  infer
3717  |  JAK2  |  infer
4023  |  LPL  |  infer
1432  |  MAPK14  |  infer
4157  |  MC1R  |  infer
4277  |  MICB  |  infer
4599  |  MX1  |  infer
4615  |  MYD88  |  infer
23114  |  NFASC  |  infer
4790  |  NFKB1  |  infer
8829  |  NRP1  |  infer
4938  |  OAS1  |  infer
4939  |  OAS2  |  infer
4940  |  OAS3  |  infer
8638  |  OASL  |  infer
51196  |  PLCE1  |  infer
5575  |  PRKAR1B  |  infer
8575  |  PRKRA  |  infer
5920  |  RARRES3  |  infer
54715  |  RBFOX1  |  infer
6041  |  RNASEL  |  infer
55072  |  RNF31  |  infer
79685  |  SAP30L  |  infer
157708  |  SEC11B  |  infer
8651  |  SOCS1  |  infer
9021  |  SOCS3  |  infer
6711  |  SPTBN1  |  infer
6772  |  STAT1  |  infer
6773  |  STAT2  |  infer
6890  |  TAP1  |  infer
6891  |  TAP2  |  infer
29110  |  TBK1  |  infer
7040  |  TGFB1  |  infer
148022  |  TICAM1  |  infer
114609  |  TIRAP  |  infer
7098  |  TLR3  |  infer
51284  |  TLR7  |  infer
51311  |  TLR8  |  infer
54106  |  TLR9  |  infer
7124  |  TNF  |  infer
7189  |  TRAF6  |  infer
23471  |  TRAM1  |  infer
7297  |  TYK2  |  infer
7299  |  TYR  |  infer
7421  |  VDR  |  infer
Text Mined Gene
Entrez_id | Symbol | Score | Resource(Total Genes:154)
8935  |  SKAP2  |  DISEASES
3385  |  ICAM3  |  DISEASES
1361  |  CPB2  |  DISEASES
4710  |  NDUFB4  |  DISEASES
359  |  AQP2  |  DISEASES
7066  |  THPO  |  DISEASES
4282  |  MIF  |  DISEASES
1723  |  DHODH  |  DISEASES
7040  |  TGFB1  |  DISEASES
7392  |  USF2  |  DISEASES
5054  |  SERPINE1  |  DISEASES
944  |  TNFSF8  |  DISEASES
6348  |  CCL3  |  DISEASES
6347  |  CCL2  |  DISEASES
3558  |  IL2  |  DISEASES
969  |  CD69  |  DISEASES
3458  |  IFNG  |  DISEASES
3565  |  IL4  |  DISEASES
28981  |  IFT81  |  DISEASES
6431  |  SRSF6  |  DISEASES
3659  |  IRF1  |  DISEASES
6351  |  CCL4  |  DISEASES
1215  |  CMA1  |  DISEASES
5894  |  RAF1  |  DISEASES
4277  |  MICB  |  DISEASES
3845  |  KRAS  |  DISEASES
10677  |  AVIL  |  DISEASES
3569  |  IL6  |  DISEASES
7450  |  VWF  |  DISEASES
3843  |  IPO5  |  DISEASES
9043  |  SPAG9  |  DISEASES
11043  |  MID2  |  DISEASES
3553  |  IL1B  |  DISEASES
64135  |  IFIH1  |  DISEASES
1656  |  DDX6  |  DISEASES
3383  |  ICAM1  |  DISEASES
10016  |  PDCD6  |  DISEASES
5286  |  PIK3C2A  |  DISEASES
1616  |  DAXX  |  DISEASES
1213  |  CLTC  |  DISEASES
125972  |  CALR3  |  DISEASES
2212  |  FCGR2A  |  DISEASES
10699  |  CORIN  |  DISEASES
3439  |  IFNA1  |  DISEASES
3606  |  IL18  |  DISEASES
90525  |  SHF  |  DISEASES
6352  |  CCL5  |  DISEASES
126820  |  WDR63  |  DISEASES
7412  |  VCAM1  |  DISEASES
213  |  ALB  |  DISEASES
5196  |  PF4  |  DISEASES
7098  |  TLR3  |  DISEASES
5724  |  PTAFR  |  DISEASES
3596  |  IL13  |  DISEASES
1051  |  CEBPB  |  DISEASES
3627  |  CXCL10  |  DISEASES
5066  |  PAM  |  DISEASES
6373  |  CXCL11  |  DISEASES
6383  |  SDC2  |  DISEASES
3799  |  KIF5B  |  DISEASES
150684  |  COMMD1  |  DISEASES
2147  |  F2  |  DISEASES
5340  |  PLG  |  DISEASES
3661  |  IRF3  |  DISEASES
285  |  ANGPT2  |  DISEASES
30835  |  CD209  |  DISEASES
6773  |  STAT2  |  DISEASES
10332  |  CLEC4M  |  DISEASES
79966  |  SCD5  |  DISEASES
149830  |  PRNT  |  DISEASES
5345  |  SERPINF2  |  DISEASES
5034  |  P4HB  |  DISEASES
6401  |  SELE  |  DISEASES
942  |  CD86  |  DISEASES
3916  |  LAMP1  |  DISEASES
2152  |  F3  |  DISEASES
1984  |  EIF5A  |  DISEASES
7317  |  UBA1  |  DISEASES
445329  |  SULT1A4  |  DISEASES
10249  |  GLYAT  |  DISEASES
4076  |  CAPRIN1  |  DISEASES
123228  |  SENP8  |  DISEASES
2537  |  IFI6  |  DISEASES
9474  |  ATG5  |  DISEASES
7177  |  TPSAB1  |  DISEASES
6818  |  SULT1A3  |  DISEASES
545  |  ATR  |  DISEASES
3455  |  IFNAR2  |  DISEASES
1003  |  CDH5  |  DISEASES
6035  |  RNASE1  |  DISEASES
7171  |  TPM4  |  DISEASES
538  |  ATP7A  |  DISEASES
302  |  ANXA2  |  DISEASES
8293  |  SERF1A  |  DISEASES
160364  |  CLEC12A  |  DISEASES
10146  |  G3BP1  |  DISEASES
22931  |  RAB18  |  DISEASES
1999  |  ELF3  |  DISEASES
9908  |  G3BP2  |  DISEASES
3123  |  HLA-DRB1  |  DISEASES
578  |  BAK1  |  DISEASES
6772  |  STAT1  |  DISEASES
10367  |  MICU1  |  DISEASES
54739  |  XAF1  |  DISEASES
4283  |  CXCL9  |  DISEASES
6993  |  DYNLT1  |  DISEASES
64710  |  NUCKS1  |  DISEASES
462  |  SERPINC1  |  DISEASES
2209  |  FCGR1A  |  DISEASES
2633  |  GBP1  |  DISEASES
60495  |  HPSE2  |  DISEASES
959  |  CD40LG  |  DISEASES
27329  |  ANGPTL3  |  DISEASES
3437  |  IFIT3  |  DISEASES
11093  |  ADAMTS13  |  DISEASES
7422  |  VEGFA  |  DISEASES
79033  |  ERI3  |  DISEASES
729238  |  SFTPA2  |  DISEASES
2833  |  CXCR3  |  DISEASES
4153  |  MBL2  |  DISEASES
7099  |  TLR4  |  DISEASES
26279  |  PLA2G2D  |  DISEASES
5320  |  PLA2G2A  |  DISEASES
23352  |  UBR4  |  DISEASES
2155  |  F7  |  DISEASES
9500  |  MAGED1  |  DISEASES
3105  |  HLA-A  |  DISEASES
7056  |  THBD  |  DISEASES
10549  |  PRDX4  |  DISEASES
23586  |  DDX58  |  DISEASES
728492  |  SERF1B  |  DISEASES
10171  |  RCL1  |  DISEASES
91543  |  RSAD2  |  DISEASES
10675  |  CSPG5  |  DISEASES
3811  |  KIR3DL1  |  DISEASES
114609  |  TIRAP  |  DISEASES
2875  |  GPT  |  DISEASES
114884  |  OSBPL10  |  DISEASES
57708  |  MIER1  |  DISEASES
8399  |  PLA2G10  |  DISEASES
87178  |  PNPT1  |  DISEASES
653509  |  SFTPA1  |  DISEASES
7124  |  TNF  |  DISEASES
3106  |  HLA-B  |  DISEASES
4049  |  LTA  |  DISEASES
388372  |  CCL4L1  |  DISEASES
3586  |  IL10  |  DISEASES
79012  |  CAMKV  |  DISEASES
30816  |  ERVW-1  |  DISEASES
51428  |  DDX41  |  DISEASES
284  |  ANGPT1  |  DISEASES
23601  |  CLEC5A  |  DISEASES
7716  |  VEZF1  |  DISEASES
284424  |  MIR7-3HG  |  DISEASES
Locus(Waiting for update.)
Disease ID 805
Disease dengue hemorrhagic fever
Integrated Phenotype(Waiting for update.)
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:19)
HP:0001873  |  Low platelet count  |  7
HP:0001945  |  Fever  |  4
HP:0001733  |  Pancreatic inflammation  |  2
HP:0001298  |  Encephalopathy  |  2
HP:0001735  |  Acute pancreatitis  |  2
HP:0002098  |  Respiratory distress  |  1
HP:0000225  |  Gingival hemorrhage  |  1
HP:0003201  |  Rhabdomyolysis  |  1
HP:0001082  |  Cholecystitis  |  1
HP:0002664  |  Neoplasia  |  1
HP:0012819  |  Myocarditis  |  1
HP:0000952  |  Yellow skin  |  1
HP:0030005  |  Capillary leak  |  1
HP:0001953  |  Diabetic ketosis  |  1
HP:0001903  |  Anemia  |  1
HP:0012223  |  Ruptured spleen  |  1
HP:0002893  |  Pituitary adenoma  |  1
HP:0012234  |  Agranulocytosis  |  1
HP:0012151  |  Hemothorax  |  1
Disease ID 805
Disease dengue hemorrhagic fever
Manually Symptom(Waiting for update.)
Text Mined Symptom
UMLS | Name | Sentences' Count(Total Symptoms:6)
C0040034  |  thrombocytopenia  |  5
C0019080  |  hemorrhage  |  3
C0009450  |  infection  |  2
C0085584  |  encephalopathy  |  2
C1282609  |  granulocytosis  |  1
C0267842  |  acute acalculous cholecystitis  |  1
Manually Genotype(Total Text Mining Genotypes:0)
(Waiting for update.)
All Snps(Total Genotypes:7)
snpId pubmedId geneId geneSymbol diseaseId sourceId sentence score Year geneSymbol_dbSNP CHROMOSOME POS REF ALT
rs12859332401673023601CLEC5Aumls:C0019100BeFreeWe demonstrated that the TT genotype of CLEC5A SNP (rs1285933 C>T) is associated with dengue severity (OR=2.25; p=0.03) and that GG genotype of -336G>A DCSIGN (CD209) SNP is associated with protection to severe dengue (OR=0.12; p=0.04).0.1205428842013CLEC5A;OR9A47141927349GA
rs12859332401673030835CD209umls:C0019100BeFreeWe demonstrated that the TT genotype of CLEC5A SNP (rs1285933 C>T) is associated with dengue severity (OR=2.25; p=0.03) and that GG genotype of -336G>A DCSIGN (CD209) SNP is associated with protection to severe dengue (OR=0.12; p=0.04).0.0008143262013CLEC5A;OR9A47141927349GA
rs1801274249119362212FCGR2Aumls:C0019100BeFreeTwo single nucleotide polymorphisms (SNPs), rs1801274 of FcγRIIa and rs4804803 of DC-SIGN, have been associated with protection from or susceptibility to severe dengue infection.0.0005428842014FCGR2A1161509955AG
rs37655242200175651196PLCE1umls:C0019100GAD[Genome-wide association study identifies susceptibility loci for dengue shock syndrome at MICB and PLCE1.]0.1226384742011PLCE11094298541CT
rs48048032124592130835CD209umls:C0019100BeFreethe rs4804803 SNP in the CD209 promoter contributed to susceptibility to dengue infection and complication of DHF.0.0008143262011CD209197747847AG
rs4804803249119362212FCGR2Aumls:C0019100BeFreeTwo single nucleotide polymorphisms (SNPs), rs1801274 of FcγRIIa and rs4804803 of DC-SIGN, have been associated with protection from or susceptibility to severe dengue infection.0.0005428842014CD209197747847AG
rs65008182200175654715RBFOX1umls:C0019100GAD[Genome-wide association study identifies susceptibility loci for dengue shock syndrome at MICB and PLCE1.]0.0023670322011RBFOX1166767374CT
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.)