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Pediatric Disease Annotations & Medicines



   chagas disease
  

Disease ID 1006
Disease chagas disease
Definition
Infection with the protozoan parasite TRYPANOSOMA CRUZI, a form of TRYPANOSOMIASIS endemic in Central and South America. It is named after the Brazilian physician Carlos Chagas, who discovered the parasite. Infection by the parasite (positive serologic result only) is distinguished from the clinical manifestations that develop years later, such as destruction of PARASYMPATHETIC GANGLIA; CHAGAS CARDIOMYOPATHY; and dysfunction of the ESOPHAGUS or COLON.
Synonym
american trypanosomiasis
chaga disease
chaga diseases
chagas dis
chagas disease [disease/finding]
chagas diseases
chagas' disease
chagas-mazza disease
cruzi infection trypanosoma
disease chagas
disease, chagas
disease, chagas'
infection by trypanosoma cruzi
infection by trypanosoma cruzi (disorder)
infection caused by trypanosoma cruzi
infection caused by trypanosoma cruzi (disorder)
south american trypanosomiasis
t cruzi
t.cruzi
trypanosomiasis, american
trypanosomiasis, brazilian
trypanosomiasis, south american
Orphanet
DOID
UMLS
C0041234
MeSH
SNOMED-CT
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:34)
C0018801  |  heart failure  |  17
C0878544  |  cardiomyopathy  |  6
C0018799  |  heart disease  |  4
C0027059  |  myocarditis  |  3
C0025164  |  megaesophagus  |  3
C0007193  |  dilated cardiomyopathy  |  2
C0085615  |  right bundle branch block  |  2
C0037280  |  infestation  |  2
C0006384  |  bundle branch block  |  2
C0018802  |  congestive heart failure  |  2
C0009806  |  constipation  |  2
C0017168  |  oesophageal reflux  |  1
C0017665  |  membranous nephropathy  |  1
C0024299  |  lymphoma  |  1
C0085615  |  right bundle-branch block  |  1
C0018801  |  cardiac failure  |  1
C0017168  |  esophageal reflux  |  1
C0017168  |  esophageal reflux disease  |  1
C0014848  |  achalasia  |  1
C0152025  |  polyneuropathy  |  1
C0018799  |  heart diseases  |  1
C0017168  |  gastroesophageal reflux  |  1
C0024301  |  follicular lymphoma  |  1
C0017168  |  gastroesophageal reflux disease  |  1
C0022658  |  nephropathy  |  1
C0398623  |  hypercoagulable state  |  1
C0041228  |  sleeping sickness  |  1
C0025160  |  megacolon  |  1
C0041228  |  african sleeping sickness  |  1
C0018799  |  cardiopathy  |  1
C0010068  |  coronary disease  |  1
C0023281  |  leishmaniasis  |  1
C0023283  |  cutaneous leishmaniasis  |  1
C0017152  |  gastritis  |  1
Curated Gene(Waiting for update.)
Inferring Gene
Entrez_id | Symbol | Resource(Total Genes:10)
6347  |  CCL2  |  infer
3117  |  HLA-DQA1  |  infer
3119  |  HLA-DQB1  |  infer
3123  |  HLA-DRB1  |  infer
3586  |  IL10  |  infer
3558  |  IL2  |  infer
3560  |  IL2RB  |  infer
3565  |  IL4  |  infer
6556  |  SLC11A1  |  infer
7124  |  TNF  |  infer
Text Mined Gene
Entrez_id | Symbol | Score | Resource(Total Genes:334)
1595  |  CYP51A1  |  DISEASES
11345  |  GABARAPL2  |  DISEASES
9341  |  VAMP3  |  DISEASES
7132  |  TNFRSF1A  |  DISEASES
8756  |  ADAM7  |  DISEASES
30009  |  TBX21  |  DISEASES
1361  |  CPB2  |  DISEASES
23409  |  SIRT4  |  DISEASES
1738  |  DLD  |  DISEASES
9552  |  SPAG7  |  DISEASES
7414  |  VCL  |  DISEASES
23411  |  SIRT1  |  DISEASES
6948  |  TCN2  |  DISEASES
158  |  ADSL  |  DISEASES
2287  |  FKBP3  |  DISEASES
3002  |  GZMB  |  DISEASES
51804  |  SIX4  |  DISEASES
1723  |  DHODH  |  DISEASES
26063  |  DECR2  |  DISEASES
2222  |  FDFT1  |  DISEASES
1666  |  DECR1  |  DISEASES
29124  |  LGALS13  |  DISEASES
973  |  CD79A  |  DISEASES
23770  |  FKBP8  |  DISEASES
1124  |  CHN2  |  DISEASES
55033  |  FKBP14  |  DISEASES
10392  |  NOD1  |  DISEASES
5118  |  PCOLCE  |  DISEASES
10105  |  PPIF  |  DISEASES
6348  |  CCL3  |  DISEASES
4353  |  MPO  |  DISEASES
6347  |  CCL2  |  DISEASES
51056  |  LAP3  |  DISEASES
3558  |  IL2  |  DISEASES
5250  |  SLC25A3  |  DISEASES
969  |  CD69  |  DISEASES
3458  |  IFNG  |  DISEASES
2597  |  GAPDH  |  DISEASES
7167  |  TPI1  |  DISEASES
29915  |  HCFC2  |  DISEASES
10475  |  TRIM38  |  DISEASES
3565  |  IL4  |  DISEASES
4953  |  ODC1  |  DISEASES
6402  |  SELL  |  DISEASES
1509  |  CTSD  |  DISEASES
10983  |  CCNI  |  DISEASES
9409  |  PEX16  |  DISEASES
84248  |  FYTTD1  |  DISEASES
11328  |  FKBP9  |  DISEASES
4035  |  LRP1  |  DISEASES
30833  |  NT5C  |  DISEASES
718  |  C3  |  DISEASES
1236  |  CCR7  |  DISEASES
22933  |  SIRT2  |  DISEASES
6351  |  CCL4  |  DISEASES
6320  |  CLEC11A  |  DISEASES
57418  |  WDR18  |  DISEASES
55902  |  ACSS2  |  DISEASES
3958  |  LGALS3  |  DISEASES
3337  |  DNAJB1  |  DISEASES
1401  |  CRP  |  DISEASES
759  |  CA1  |  DISEASES
8932  |  MBD2  |  DISEASES
4064  |  CD180  |  DISEASES
50640  |  PNPLA8  |  DISEASES
3915  |  LAMC1  |  DISEASES
3569  |  IL6  |  DISEASES
7097  |  TLR2  |  DISEASES
7057  |  THBS1  |  DISEASES
9360  |  PPIG  |  DISEASES
5858  |  PZP  |  DISEASES
23316  |  CUX2  |  DISEASES
8766  |  RAB11A  |  DISEASES
23361  |  ZNF629  |  DISEASES
6845  |  VAMP7  |  DISEASES
3959  |  LGALS3BP  |  DISEASES
3552  |  IL1A  |  DISEASES
3553  |  IL1B  |  DISEASES
9066  |  SYT7  |  DISEASES
4811  |  NID1  |  DISEASES
941  |  CD80  |  DISEASES
790  |  CAD  |  DISEASES
3383  |  ICAM1  |  DISEASES
3827  |  KNG1  |  DISEASES
2028  |  ENPEP  |  DISEASES
57678  |  GPAM  |  DISEASES
55749  |  CCAR1  |  DISEASES
1795  |  DOCK3  |  DISEASES
23710  |  GABARAPL1  |  DISEASES
8620  |  NPFF  |  DISEASES
3687  |  ITGAX  |  DISEASES
207  |  AKT1  |  DISEASES
5226  |  PGD  |  DISEASES
57530  |  CGN  |  DISEASES
805  |  CALM2  |  DISEASES
5868  |  RAB5A  |  DISEASES
1609  |  DGKQ  |  DISEASES
100996939  |  PYURF  |  DISEASES
3001  |  GZMA  |  DISEASES
4915  |  NTRK2  |  DISEASES
3606  |  IL18  |  DISEASES
60558  |  GUF1  |  DISEASES
83734  |  ATG10  |  DISEASES
2697  |  GJA1  |  DISEASES
9453  |  GGPS1  |  DISEASES
1360  |  CPB1  |  DISEASES
925  |  CD8A  |  DISEASES
22934  |  RPIA  |  DISEASES
9407  |  TMPRSS11D  |  DISEASES
760  |  CA2  |  DISEASES
761  |  CA3  |  DISEASES
7547  |  ZIC3  |  DISEASES
1636  |  ACE  |  DISEASES
808  |  CALM3  |  DISEASES
2220  |  FCN2  |  DISEASES
115653  |  KIR3DL3  |  DISEASES
729230  |  CCR2  |  DISEASES
1234  |  CCR5  |  DISEASES
4061  |  LY6E  |  DISEASES
6352  |  CCL5  |  DISEASES
7412  |  VCAM1  |  DISEASES
2215  |  FCGR3B  |  DISEASES
4880  |  NPPC  |  DISEASES
132954  |  PDCL2  |  DISEASES
213  |  ALB  |  DISEASES
25976  |  TIPARP  |  DISEASES
1230  |  CCR1  |  DISEASES
5648  |  MASP1  |  DISEASES
1437  |  CSF2  |  DISEASES
3251  |  HPRT1  |  DISEASES
5267  |  SERPINA4  |  DISEASES
10576  |  CCT2  |  DISEASES
762  |  CA4  |  DISEASES
3308  |  HSPA4  |  DISEASES
1493  |  CTLA4  |  DISEASES
7064  |  THOP1  |  DISEASES
7275  |  TUB  |  DISEASES
10484  |  SEC23A  |  DISEASES
79893  |  GGNBP2  |  DISEASES
624  |  BDKRB2  |  DISEASES
1938  |  EEF2  |  DISEASES
285704  |  RGMB  |  DISEASES
5897  |  RAG2  |  DISEASES
763  |  CA5A  |  DISEASES
23536  |  ADAT1  |  DISEASES
8061  |  FOSL1  |  DISEASES
26512  |  INTS6  |  DISEASES
2286  |  FKBP2  |  DISEASES
10007  |  GNPDA1  |  DISEASES
80818  |  ZNF436  |  DISEASES
92745  |  SLC38A5  |  DISEASES
8636  |  SSNA1  |  DISEASES
1604  |  CD55  |  DISEASES
60681  |  FKBP10  |  DISEASES
6950  |  TCP1  |  DISEASES
8542  |  APOL1  |  DISEASES
8411  |  EEA1  |  DISEASES
23621  |  BACE1  |  DISEASES
811  |  CALR  |  DISEASES
6863  |  TAC1  |  DISEASES
1153  |  CIRBP  |  DISEASES
2  |  A2M  |  DISEASES
85302  |  FBF1  |  DISEASES
148266  |  ZNF569  |  DISEASES
9033  |  PKD2L1  |  DISEASES
3628  |  INPP1  |  DISEASES
10250  |  SRRM1  |  DISEASES
4191  |  MDH2  |  DISEASES
4843  |  NOS2  |  DISEASES
1606  |  DGKA  |  DISEASES
51547  |  SIRT7  |  DISEASES
9021  |  SOCS3  |  DISEASES
2520  |  GAST  |  DISEASES
6401  |  SELE  |  DISEASES
942  |  CD86  |  DISEASES
8398  |  PLA2G6  |  DISEASES
3916  |  LAMP1  |  DISEASES
27152  |  INTU  |  DISEASES
3320  |  HSP90AA1  |  DISEASES
1103  |  CHAT  |  DISEASES
51548  |  SIRT6  |  DISEASES
4842  |  NOS1  |  DISEASES
57142  |  RTN4  |  DISEASES
5269  |  SERPINB6  |  DISEASES
1368  |  CPM  |  DISEASES
8835  |  SOCS2  |  DISEASES
23193  |  GANAB  |  DISEASES
669  |  BPGM  |  DISEASES
1508  |  CTSB  |  DISEASES
2272  |  FHIT  |  DISEASES
921  |  CD5  |  DISEASES
9474  |  ATG5  |  DISEASES
3605  |  IL17A  |  DISEASES
766  |  CA7  |  DISEASES
64094  |  SMOC2  |  DISEASES
79971  |  WLS  |  DISEASES
85301  |  COL27A1  |  DISEASES
4624  |  MYH6  |  DISEASES
2224  |  FDPS  |  DISEASES
8794  |  TNFRSF10C  |  DISEASES
246778  |  IL27  |  DISEASES
801  |  CALM1  |  DISEASES
85569  |  GALP  |  DISEASES
1121  |  CHM  |  DISEASES
51592  |  TRIM33  |  DISEASES
6364  |  CCL20  |  DISEASES
1995  |  ELAVL3  |  DISEASES
51150  |  SDF4  |  DISEASES
6693  |  SPN  |  DISEASES
1523  |  CUX1  |  DISEASES
5575  |  PRKAR1B  |  DISEASES
58484  |  NLRC4  |  DISEASES
4916  |  NTRK3  |  DISEASES
4512  |  MT-CO1  |  DISEASES
4519  |  MT-CYB  |  DISEASES
4540  |  MT-ND5  |  DISEASES
4513  |  MT-CO2  |  DISEASES
4283  |  CXCL9  |  DISEASES
4538  |  MT-ND4  |  DISEASES
7179  |  TPTE  |  DISEASES
23038  |  WDTC1  |  DISEASES
23456  |  ABCB10  |  DISEASES
7432  |  VIP  |  DISEASES
5788  |  PTPRC  |  DISEASES
259266  |  ASPM  |  DISEASES
3080  |  CFHR2  |  DISEASES
10090  |  UST  |  DISEASES
10981  |  RAB32  |  DISEASES
356  |  FASLG  |  DISEASES
2214  |  FCGR3A  |  DISEASES
912  |  CD1D  |  DISEASES
262  |  AMD1  |  DISEASES
1520  |  CTSS  |  DISEASES
153  |  ADRB1  |  DISEASES
4803  |  NGF  |  DISEASES
57038  |  RARS2  |  DISEASES
9892  |  SNAP91  |  DISEASES
515  |  ATP5F1  |  DISEASES
728447  |  TEX28P1  |  DISEASES
653363  |  TEX28P2  |  DISEASES
23443  |  SLC35A3  |  DISEASES
253152  |  EPHX4  |  DISEASES
4923  |  NTSR1  |  DISEASES
959  |  CD40LG  |  DISEASES
51442  |  VGLL1  |  DISEASES
9406  |  ZRANB2  |  DISEASES
4070  |  TACSTD2  |  DISEASES
9481  |  SLC25A27  |  DISEASES
377841  |  ENTPD8  |  DISEASES
2030  |  SLC29A1  |  DISEASES
6130  |  RPL7A  |  DISEASES
26301  |  GBGT1  |  DISEASES
958  |  CD40  |  DISEASES
100  |  ADA  |  DISEASES
90550  |  MCU  |  DISEASES
8879  |  SGPL1  |  DISEASES
5464  |  PPA1  |  DISEASES
2833  |  CXCR3  |  DISEASES
253430  |  IPMK  |  DISEASES
4153  |  MBL2  |  DISEASES
7099  |  TLR4  |  DISEASES
6572  |  SLC18A3  |  DISEASES
1896  |  EDA  |  DISEASES
5698  |  PSMB9  |  DISEASES
5696  |  PSMB8  |  DISEASES
27301  |  APEX2  |  DISEASES
5207  |  PFKFB1  |  DISEASES
26279  |  PLA2G2D  |  DISEASES
4758  |  NEU1  |  DISEASES
7917  |  BAG6  |  DISEASES
4795  |  NFKBIL1  |  DISEASES
50943  |  FOXP3  |  DISEASES
4879  |  NPPB  |  DISEASES
4878  |  NPPA  |  DISEASES
5305  |  PIP4K2A  |  DISEASES
116511  |  MAS1L  |  DISEASES
765  |  CA6  |  DISEASES
23408  |  SIRT5  |  DISEASES
1906  |  EDN1  |  DISEASES
3559  |  IL2RA  |  DISEASES
284390  |  ZNF763  |  DISEASES
57486  |  NLN  |  DISEASES
55858  |  TMEM165  |  DISEASES
55806  |  HR  |  DISEASES
5555  |  PRH2  |  DISEASES
80333  |  KCNIP4  |  DISEASES
23410  |  SIRT3  |  DISEASES
5268  |  SERPINB5  |  DISEASES
3875  |  KRT18  |  DISEASES
114609  |  TIRAP  |  DISEASES
654364  |  NME1-NME2  |  DISEASES
115560  |  ZNF501  |  DISEASES
7919  |  DDX39B  |  DISEASES
6843  |  VAMP1  |  DISEASES
3652  |  IPP  |  DISEASES
594857  |  NPS  |  DISEASES
4905  |  NSF  |  DISEASES
10747  |  MASP2  |  DISEASES
56903  |  PAPOLB  |  DISEASES
3267  |  AGFG1  |  DISEASES
4125  |  MAN2B1  |  DISEASES
1719  |  DHFR  |  DISEASES
50863  |  NTM  |  DISEASES
22809  |  ATF5  |  DISEASES
960  |  CD44  |  DISEASES
7124  |  TNF  |  DISEASES
4615  |  MYD88  |  DISEASES
161497  |  STRC  |  DISEASES
26054  |  SENP6  |  DISEASES
4049  |  LTA  |  DISEASES
26168  |  SENP3  |  DISEASES
9732  |  DOCK4  |  DISEASES
84671  |  ZNF347  |  DISEASES
2821  |  GPI  |  DISEASES
89782  |  LMLN  |  DISEASES
3586  |  IL10  |  DISEASES
5554  |  PRH1  |  DISEASES
721  |  C4B  |  DISEASES
8801  |  SUCLG2  |  DISEASES
127933  |  UHMK1  |  DISEASES
51428  |  DDX41  |  DISEASES
9140  |  ATG12  |  DISEASES
4914  |  NTRK1  |  DISEASES
4586  |  MUC5AC  |  DISEASES
930  |  CD19  |  DISEASES
4190  |  MDH1  |  DISEASES
1622  |  DBI  |  DISEASES
80790  |  CMIP  |  DISEASES
51303  |  FKBP11  |  DISEASES
10490  |  VTI1B  |  DISEASES
2232  |  FDXR  |  DISEASES
4782  |  NFIC  |  DISEASES
246734  |  NPCDR1  |  DISEASES
102723508  |  KANTR  |  DISEASES
Locus(Waiting for update.)
Disease ID 1006
Disease chagas disease
Integrated Phenotype(Waiting for update.)
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:25)
HP:0001635  |  Congestive heart failure  |  19
HP:0001638  |  Cardiomyopathy  |  6
HP:0011675  |  Arrhythmias  |  6
HP:0001297  |  Cerebral vascular events  |  4
HP:0004308  |  Ventricular arrhythmia  |  4
HP:0011710  |  Bundle-branch block  |  3
HP:0011712  |  Right bundle-branch block  |  3
HP:0012819  |  Myocarditis  |  3
HP:0001644  |  Congestive cardiomyopathy  |  2
HP:0002459  |  Dysautonomia  |  2
HP:0002019  |  Dyschezia  |  2
HP:0002960  |  Autoimmune condition  |  2
HP:0001263  |  Developmental retardation  |  1
HP:0001271  |  Polyneuropathy  |  1
HP:0000112  |  Nephropathy  |  1
HP:0002665  |  Lymphoma  |  1
HP:0005263  |  Gastritis  |  1
HP:0002251  |  Hirschsprung megacolon  |  1
HP:0001677  |  Coronary artery disease  |  1
HP:0002571  |  Achalasia  |  1
HP:0100749  |  Thoracic pain  |  1
HP:0012531  |  Pain  |  1
HP:0012266  |  T-wave alternans  |  1
HP:0012578  |  Membranous glomerulonephritis  |  1
HP:0002020  |  Heartburn  |  1
Disease ID 1006
Disease chagas disease
Manually Symptom(Waiting for update.)
Text Mined Symptom
UMLS | Name | Sentences' Count(Total Symptoms:12)
C0018801  |  heart failure  |  17
C0878544  |  cardiomyopathy  |  6
C0038454  |  stroke  |  4
C0027059  |  myocarditis  |  3
C0021311  |  infections  |  3
C0018802  |  congestive heart failure  |  2
C0007193  |  dilated cardiomyopathy  |  2
C0014848  |  achalasia  |  1
C0018801  |  cardiac failure  |  1
C0152025  |  polyneuropathy  |  1
C0018799  |  cardiopathy  |  1
C0025160  |  megacolon  |  1
Manually Genotype(Total Text Mining Genotypes:0)
(Waiting for update.)
All Snps(Total Genotypes:5)
snpId pubmedId geneId geneSymbol diseaseId sourceId sentence score Year geneSymbol_dbSNP CHROMOSOME POS REF ALT
rs2043055257432413606IL18umls:C0041234BeFreeWe analyzed the rs2043055 marker in the IL18 gene in a cohort of Chagas disease cardiomyopathy patients (n=849) and asymptomatic subjects (n=202).0.0002714422015IL1811112160901AG
rs386502799194562347097TLR2umls:C0041234BeFreeT. cruzi-infected individuals who are heterozygous for the MAL/TIRAP S180L variant that leads to a decrease in signal transduction upon ligation of TLR2 or TLR4 to their respective ligand may have a lower risk of developing CCC.0.0008143262009NANANANANA
rs38650279919456234114609TIRAPumls:C0041234BeFreeT. cruzi-infected individuals who are heterozygous for the MAL/TIRAP S180L variant that leads to a decrease in signal transduction upon ligation of TLR2 or TLR4 to their respective ligand may have a lower risk of developing CCC.0.0002714422009NANANANANA
rs8177374194562347097TLR2umls:C0041234BeFreeT. cruzi-infected individuals who are heterozygous for the MAL/TIRAP S180L variant that leads to a decrease in signal transduction upon ligation of TLR2 or TLR4 to their respective ligand may have a lower risk of developing CCC.0.0008143262009TIRAP11126292948CT
rs817737419456234114609TIRAPumls:C0041234BeFreeT. cruzi-infected individuals who are heterozygous for the MAL/TIRAP S180L variant that leads to a decrease in signal transduction upon ligation of TLR2 or TLR4 to their respective ligand may have a lower risk of developing CCC.0.0002714422009TIRAP11126292948CT
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.)