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Pediatric Disease Annotations & Medicines



   dengue shock syndrome
  

Disease ID 1728
Disease dengue shock syndrome
Synonym
dengue shock syndrome (disorder)
DOID
UMLS
C0376300
SNOMED-CT
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:4)
C0019100  |  dengue hemorrhagic fever  |  2
C0040034  |  thrombocytopenia  |  1
C0024291  |  hemophagocytic syndrome  |  1
C0014038  |  encephalitis  |  1
Curated Gene
Entrez_id | Symbol | Resource(Total Genes:3)
MICB  |  4277  |  GWASCAT
RBFOX1  |  54715  |  GWASCAT
PLCE1  |  51196  |  GWASCAT
Inferring Gene(Waiting for update.)
Text Mined Gene
Entrez_id | Symbol | Score | Resource(Total Genes:137)
1634  |  DCN  |  DISEASES
3385  |  ICAM3  |  DISEASES
4282  |  MIF  |  DISEASES
10544  |  PROCR  |  DISEASES
1457  |  CSNK2A1  |  DISEASES
10562  |  OLFM4  |  DISEASES
1723  |  DHODH  |  DISEASES
5327  |  PLAT  |  DISEASES
5054  |  SERPINE1  |  DISEASES
944  |  TNFSF8  |  DISEASES
6347  |  CCL2  |  DISEASES
3458  |  IFNG  |  DISEASES
55907  |  CMAS  |  DISEASES
3565  |  IL4  |  DISEASES
3769  |  KCNJ13  |  DISEASES
28981  |  IFT81  |  DISEASES
5740  |  PTGIS  |  DISEASES
3659  |  IRF1  |  DISEASES
2658  |  GDF2  |  DISEASES
1215  |  CMA1  |  DISEASES
5894  |  RAF1  |  DISEASES
4277  |  MICB  |  DISEASES
3845  |  KRAS  |  DISEASES
10677  |  AVIL  |  DISEASES
3569  |  IL6  |  DISEASES
51196  |  PLCE1  |  DISEASES
6857  |  SYT1  |  DISEASES
7305  |  TYROBP  |  DISEASES
671  |  BPI  |  DISEASES
1434  |  CSE1L  |  DISEASES
3553  |  IL1B  |  DISEASES
64135  |  IFIH1  |  DISEASES
8850  |  KAT2B  |  DISEASES
10578  |  GNLY  |  DISEASES
1656  |  DDX6  |  DISEASES
3383  |  ICAM1  |  DISEASES
10016  |  PDCD6  |  DISEASES
1616  |  DAXX  |  DISEASES
429  |  ASCL1  |  DISEASES
5409  |  PNMT  |  DISEASES
2212  |  FCGR2A  |  DISEASES
3439  |  IFNA1  |  DISEASES
7082  |  TJP1  |  DISEASES
6352  |  CCL5  |  DISEASES
7412  |  VCAM1  |  DISEASES
213  |  ALB  |  DISEASES
2562  |  GABRB3  |  DISEASES
116071  |  BATF2  |  DISEASES
5729  |  PTGDR  |  DISEASES
1051  |  CEBPB  |  DISEASES
3627  |  CXCL10  |  DISEASES
50515  |  CHST11  |  DISEASES
2243  |  FGA  |  DISEASES
3669  |  ISG20  |  DISEASES
6373  |  CXCL11  |  DISEASES
3799  |  KIF5B  |  DISEASES
113189  |  CHST14  |  DISEASES
2147  |  F2  |  DISEASES
5340  |  PLG  |  DISEASES
3661  |  IRF3  |  DISEASES
285  |  ANGPT2  |  DISEASES
30835  |  CD209  |  DISEASES
6773  |  STAT2  |  DISEASES
10332  |  CLEC4M  |  DISEASES
64388  |  GREM2  |  DISEASES
6819  |  SULT1C2  |  DISEASES
149830  |  PRNT  |  DISEASES
6478  |  SIAH2  |  DISEASES
8844  |  KSR1  |  DISEASES
7329  |  UBE2I  |  DISEASES
3665  |  IRF7  |  DISEASES
2152  |  F3  |  DISEASES
1984  |  EIF5A  |  DISEASES
7317  |  UBA1  |  DISEASES
445329  |  SULT1A4  |  DISEASES
4076  |  CAPRIN1  |  DISEASES
123228  |  SENP8  |  DISEASES
1544  |  CYP1A2  |  DISEASES
2537  |  IFI6  |  DISEASES
5348  |  FXYD1  |  DISEASES
7177  |  TPSAB1  |  DISEASES
6818  |  SULT1A3  |  DISEASES
545  |  ATR  |  DISEASES
3455  |  IFNAR2  |  DISEASES
1003  |  CDH5  |  DISEASES
8720  |  MBTPS1  |  DISEASES
538  |  ATP7A  |  DISEASES
8293  |  SERF1A  |  DISEASES
100506658  |  OCLN  |  DISEASES
160364  |  CLEC12A  |  DISEASES
10146  |  G3BP1  |  DISEASES
22931  |  RAB18  |  DISEASES
404552  |  SCGB1D4  |  DISEASES
9908  |  G3BP2  |  DISEASES
6772  |  STAT1  |  DISEASES
10367  |  MICU1  |  DISEASES
54739  |  XAF1  |  DISEASES
4283  |  CXCL9  |  DISEASES
2209  |  FCGR1A  |  DISEASES
60495  |  HPSE2  |  DISEASES
959  |  CD40LG  |  DISEASES
27329  |  ANGPTL3  |  DISEASES
3437  |  IFIT3  |  DISEASES
79033  |  ERI3  |  DISEASES
2833  |  CXCR3  |  DISEASES
2155  |  F7  |  DISEASES
3190  |  HNRNPK  |  DISEASES
1041  |  CDSN  |  DISEASES
3105  |  HLA-A  |  DISEASES
7056  |  THBD  |  DISEASES
5100  |  PCDH8  |  DISEASES
388585  |  HES5  |  DISEASES
9308  |  CD83  |  DISEASES
23586  |  DDX58  |  DISEASES
3704  |  ITPA  |  DISEASES
728492  |  SERF1B  |  DISEASES
91543  |  RSAD2  |  DISEASES
1761  |  DMRT1  |  DISEASES
10675  |  CSPG5  |  DISEASES
2875  |  GPT  |  DISEASES
10379  |  IRF9  |  DISEASES
2909  |  ARHGAP35  |  DISEASES
57703  |  CWC22  |  DISEASES
87178  |  PNPT1  |  DISEASES
85443  |  DCLK3  |  DISEASES
7124  |  TNF  |  DISEASES
5923  |  RASGRF1  |  DISEASES
3586  |  IL10  |  DISEASES
30816  |  ERVW-1  |  DISEASES
51428  |  DDX41  |  DISEASES
284  |  ANGPT1  |  DISEASES
55656  |  INTS8  |  DISEASES
23601  |  CLEC5A  |  DISEASES
56342  |  PPAN  |  DISEASES
7716  |  VEZF1  |  DISEASES
284424  |  MIR7-3HG  |  DISEASES
7955  |  RNF217-AS1  |  DISEASES
Locus(Waiting for update.)
Disease ID 1728
Disease dengue shock syndrome
Integrated Phenotype(Waiting for update.)
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:6)
HP:0002615  |  Low blood pressure  |  3
HP:0001873  |  Low platelet count  |  1
HP:0001399  |  Liver failure  |  1
HP:0002098  |  Respiratory distress  |  1
HP:0002383  |  Encephalitis  |  1
HP:0001945  |  Fever  |  1
Disease ID 1728
Disease dengue shock syndrome
Manually Symptom(Waiting for update.)
Text Mined Symptom
UMLS | Name | Sentences' Count(Total Symptoms: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
rs31324682353685751196PLCE1umls:C0376300BeFreeThis study confirms that the MICB rs3132468 and PLCE1 rs3740360 risk genotypes are not only associated with DSS, but are also associated with less severe clinical phenotypes of dengue, as well as with dengue in infants.0.1205428842013MICB631507709CT
rs3132468220017564277MICBumls:C0376300GWASCATGenome-wide association study identifies susceptibility loci for dengue shock syndrome at MICB and PLCE1.0.1202714422011MICB631507709CT
rs3132468235368574277MICBumls:C0376300BeFreeThis study confirms that the MICB rs3132468 and PLCE1 rs3740360 risk genotypes are not only associated with DSS, but are also associated with less severe clinical phenotypes of dengue, as well as with dengue in infants.0.1202714422013MICB631507709CT
rs3740360235368574277MICBumls:C0376300BeFreeThis study confirms that the MICB rs3132468 and PLCE1 rs3740360 risk genotypes are not only associated with DSS, but are also associated with less severe clinical phenotypes of dengue, as well as with dengue in infants.0.1202714422013PLCE11094265734AC
rs37403602353685751196PLCE1umls:C0376300BeFreeThis study confirms that the MICB rs3132468 and PLCE1 rs3740360 risk genotypes are not only associated with DSS, but are also associated with less severe clinical phenotypes of dengue, as well as with dengue in infants.0.1205428842013PLCE11094265734AC
rs37655242200175651196PLCE1umls:C0376300GWASCATGenome-wide association study identifies susceptibility loci for dengue shock syndrome at MICB and PLCE1.0.1205428842011PLCE11094298541CT
rs65008182200175654715RBFOX1umls:C0376300GWASCATGenome-wide association study identifies susceptibility loci for dengue shock syndrome at MICB and PLCE1.0.122011RBFOX1166767374CT
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.)