Home Contact Sitemap

eRAM

encyclopedia of Rare Disease Annotation for Precision Medicine



   peripheral t-cell lymphoma
  

Disease ID 1397
Disease peripheral t-cell lymphoma
Definition
A group of malignant lymphomas thought to derive from peripheral T-lymphocytes in lymph nodes and other nonlymphoid sites. They include a broad spectrum of lymphocyte morphology, but in all instances express T-cell markers admixed with epithelioid histiocytes, plasma cells, and eosinophils. Although markedly similar to large-cell immunoblastic lymphoma (LYMPHOMA, LARGE-CELL, IMMUNOBLASTIC), this group's unique features warrant separate treatment.
Synonym
[m] peripheral t-cell lymphoma nos
[m] peripheral t-cell lymphoma nos (morphologic abnormality)
cell lymphomas peripheral t
lymphoma, peripheral t-cell
lymphoma, t cell, peripheral
lymphoma, t-cell, peripheral
lymphoma, t-cell, peripheral [disease/finding]
lymphomas, peripheral t-cell
mature t-and nk-cell lymphoma
mature t-cell and nk-cell lymphoma
mature t-cell and nk-cell non-hodgkin lymphoma
mature t-cell and nk-cell non-hodgkin's lymphoma
mature t-cell lymphoma
mature t-cell non-hodgkin's lymphoma
peripheral t cell lymphoma
peripheral t-cell lymphoma (clinical)
peripheral t-cell lymphoma (disorder)
peripheral t-cell lymphoma (morphologic abnormality)
peripheral t-cell lymphoma unspecified
peripheral t-cell lymphoma, no icd-o subtype
peripheral t-cell lymphoma, no icd-o subtype (morphologic abnormality)
peripheral t-cell lymphoma, no international classification of diseases for oncology subtype
peripheral t-cell lymphoma, no international classification of diseases for oncology subtype (morphologic abnormality)
peripheral t-cell lymphoma, nos
peripheral t-cell lymphoma, not otherwise specified
peripheral t-cell lymphomas
ptcl
t cell lymphoma, peripheral
t-cell lymphoma, peripheral
t-cell lymphomas, peripheral
DOID
UMLS
C0079774
MeSH
SNOMED-CT
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:30)
C0024299  |  lymphoma  |  6
C0024299  |  lymphomas  |  3
C0024312  |  lymphopenia  |  2
C0024305  |  non-hodgkin lymphoma  |  1
C0030807  |  pemphigus  |  1
C0079731  |  b-cell non-hodgkin lymphoma  |  1
C0024314  |  lymphoproliferative disorder  |  1
C0206180  |  anaplastic large-cell lymphoma  |  1
C0007570  |  celiac disease  |  1
C0021831  |  enteropathy  |  1
C0001815  |  myelofibrosis  |  1
C0085652  |  pyoderma gangrenosum  |  1
C0014013  |  pyothorax  |  1
C0027809  |  schwannoma  |  1
C0221026  |  x-linked agammaglobulinaemia  |  1
C0024291  |  hemophagocytic syndrome  |  1
C0206141  |  hypereosinophilic syndrome  |  1
C0206674  |  villous adenoma  |  1
C0027726  |  nephrotic syndrome  |  1
C0221032  |  generalized lipodystrophy  |  1
C0019829  |  hodgkin lymphoma  |  1
C0206180  |  anaplastic large cell lymphoma  |  1
C0024302  |  large cell lymphoma  |  1
C0079774  |  peripheral t-cell lymphoma  |  1
C0034212  |  pyoderma  |  1
C0010346  |  crohn's disease  |  1
C0023787  |  lipodystrophy  |  1
C0079748  |  lymphoblastic lymphoma  |  1
C0036421  |  systemic sclerosis  |  1
C0024314  |  lymphoproliferative disorders  |  1
Curated Gene
Entrez_id | Symbol | Resource(Total Genes:9)
2534  |  FYN  |  CTD_human
3418  |  IDH2  |  CTD_human
1788  |  DNMT3A  |  CTD_human
54790  |  TET2  |  CTD_human
567  |  B2M  |  CTD_human
472  |  ATM  |  CTD_human
387  |  RHOA  |  CTD_human
965  |  CD58  |  CTD_human
940  |  CD28  |  CTD_human
Inferring Gene(Waiting for update.)
Text Mined Gene
Entrez_id | Symbol | Score | Resource(Total Genes:370)
100  |  ADA  |  1.998  |  DISEASES
100  |  ADA  |  1.997  |  DISEASES
51390  |  AIG1  |  2.255  |  DISEASES
51390  |  AIG1  |  2.254  |  DISEASES
202  |  AIM1  |  2.035  |  DISEASES
202  |  AIM1  |  2.034  |  DISEASES
238  |  ALK  |  4.713  |  DISEASES
238  |  ALK  |  4.713  |  DISEASES
257  |  ALX3  |  1.017  |  DISEASES
257  |  ALX3  |  1.016  |  DISEASES
51378  |  ANGPT4  |  1.034  |  DISEASES
51378  |  ANGPT4  |  1.034  |  DISEASES
83478  |  ARHGAP24  |  1.409  |  DISEASES
83478  |  ARHGAP24  |  1.409  |  DISEASES
64225  |  ATL2  |  1.119  |  DISEASES
64225  |  ATL2  |  1.118  |  DISEASES
25923  |  ATL3  |  1.941  |  DISEASES
25923  |  ATL3  |  1.941  |  DISEASES
567  |  B2M  |  2.394  |  DISEASES
567  |  B2M  |  2.393  |  DISEASES
64919  |  BCL11B  |  1.312  |  DISEASES
64919  |  BCL11B  |  1.312  |  DISEASES
10018  |  BCL2L11  |  1.352  |  DISEASES
10018  |  BCL2L11  |  1.352  |  DISEASES
605  |  BCL7A  |  2.896  |  DISEASES
605  |  BCL7A  |  2.895  |  DISEASES
65980  |  BRD9  |  1.401  |  DISEASES
65980  |  BRD9  |  1.401  |  DISEASES
79886  |  CAAP1  |  1.301  |  DISEASES
79886  |  CAAP1  |  1.301  |  DISEASES
781  |  CACNA2D1  |  1.053  |  DISEASES
781  |  CACNA2D1  |  1.053  |  DISEASES
147968  |  CAPN12  |  2.214  |  DISEASES
147968  |  CAPN12  |  2.213  |  DISEASES
84433  |  CARD11  |  2.323  |  DISEASES
84433  |  CARD11  |  2.322  |  DISEASES
841  |  CASP8  |  1.175  |  DISEASES
841  |  CASP8  |  1.174  |  DISEASES
25901  |  CCDC28A  |  1.938  |  DISEASES
25901  |  CCDC28A  |  1.938  |  DISEASES
80323  |  CCDC68  |  1.675  |  DISEASES
80323  |  CCDC68  |  1.674  |  DISEASES
6364  |  CCL20  |  1.663  |  DISEASES
6364  |  CCL20  |  1.662  |  DISEASES
1232  |  CCR3  |  2.318  |  DISEASES
1232  |  CCR3  |  2.318  |  DISEASES
1233  |  CCR4  |  1.724  |  DISEASES
1233  |  CCR4  |  1.724  |  DISEASES
1237  |  CCR8  |  1.719  |  DISEASES
1237  |  CCR8  |  1.719  |  DISEASES
9332  |  CD163  |  2.31  |  DISEASES
9332  |  CD163  |  2.309  |  DISEASES
930  |  CD19  |  2.426  |  DISEASES
930  |  CD19  |  2.425  |  DISEASES
914  |  CD2  |  5.274  |  DISEASES
914  |  CD2  |  5.274  |  DISEASES
50489  |  CD207  |  2.12  |  DISEASES
50489  |  CD207  |  2.12  |  DISEASES
29126  |  CD274  |  1.016  |  DISEASES
29126  |  CD274  |  1.016  |  DISEASES
959  |  CD40LG  |  2.708  |  DISEASES
959  |  CD40LG  |  2.708  |  DISEASES
921  |  CD5  |  5.119  |  DISEASES
921  |  CD5  |  5.118  |  DISEASES
1043  |  CD52  |  4.32  |  DISEASES
1043  |  CD52  |  4.319  |  DISEASES
9308  |  CD83  |  1.843  |  DISEASES
9308  |  CD83  |  1.842  |  DISEASES
942  |  CD86  |  1.51  |  DISEASES
942  |  CD86  |  1.509  |  DISEASES
1029  |  CDKN2A  |  2.359  |  DISEASES
1029  |  CDKN2A  |  2.358  |  DISEASES
1107  |  CHD3  |  1.096  |  DISEASES
1107  |  CHD3  |  1.095  |  DISEASES
170482  |  CLEC4C  |  1.098  |  DISEASES
170482  |  CLEC4C  |  1.097  |  DISEASES
163882  |  CNST  |  2.08  |  DISEASES
163882  |  CNST  |  2.079  |  DISEASES
1378  |  CR1  |  2.258  |  DISEASES
1378  |  CR1  |  2.257  |  DISEASES
1380  |  CR2  |  3.255  |  DISEASES
1380  |  CR2  |  3.255  |  DISEASES
64693  |  CTAGE1  |  2.026  |  DISEASES
64693  |  CTAGE1  |  2.025  |  DISEASES
6387  |  CXCL12  |  1.14  |  DISEASES
6387  |  CXCL12  |  1.14  |  DISEASES
284340  |  CXCL17  |  1.546  |  DISEASES
284340  |  CXCL17  |  1.546  |  DISEASES
4283  |  CXCL9  |  2.065  |  DISEASES
4283  |  CXCL9  |  2.065  |  DISEASES
2833  |  CXCR3  |  3.471  |  DISEASES
2833  |  CXCR3  |  3.47  |  DISEASES
7852  |  CXCR4  |  1.361  |  DISEASES
7852  |  CXCR4  |  1.361  |  DISEASES
26052  |  DNM3  |  2.058  |  DISEASES
26052  |  DNM3  |  2.058  |  DISEASES
1791  |  DNTT  |  2.184  |  DISEASES
1791  |  DNTT  |  2.184  |  DISEASES
1803  |  DPP4  |  3.489  |  DISEASES
1803  |  DPP4  |  3.489  |  DISEASES
56940  |  DUSP22  |  2.984  |  DISEASES
56940  |  DUSP22  |  2.983  |  DISEASES
10938  |  EHD1  |  1.454  |  DISEASES
10938  |  EHD1  |  1.454  |  DISEASES
10209  |  EIF1  |  1.245  |  DISEASES
10209  |  EIF1  |  1.244  |  DISEASES
8667  |  EIF3H  |  1.119  |  DISEASES
8667  |  EIF3H  |  1.119  |  DISEASES
30816  |  ERVW-1  |  2.805  |  DISEASES
30816  |  ERVW-1  |  2.804  |  DISEASES
355  |  FAS  |  2.784  |  DISEASES
355  |  FAS  |  2.784  |  DISEASES
100302740  |  FAS-AS1  |  1.508  |  DISEASES
100302740  |  FAS-AS1  |  1.508  |  DISEASES
356  |  FASLG  |  2.504  |  DISEASES
356  |  FASLG  |  2.503  |  DISEASES
2214  |  FCGR3A  |  2.761  |  DISEASES
2214  |  FCGR3A  |  2.76  |  DISEASES
115352  |  FCRL3  |  1.846  |  DISEASES
115352  |  FCRL3  |  1.846  |  DISEASES
344018  |  FIGLA  |  1.653  |  DISEASES
344018  |  FIGLA  |  1.652  |  DISEASES
2290  |  FOXG1  |  2.044  |  DISEASES
2290  |  FOXG1  |  2.043  |  DISEASES
50943  |  FOXP3  |  3.397  |  DISEASES
50943  |  FOXP3  |  3.396  |  DISEASES
6624  |  FSCN1  |  1.297  |  DISEASES
6624  |  FSCN1  |  1.296  |  DISEASES
2526  |  FUT4  |  3.444  |  DISEASES
2526  |  FUT4  |  3.444  |  DISEASES
2625  |  GATA3  |  2.364  |  DISEASES
2625  |  GATA3  |  2.364  |  DISEASES
115362  |  GBP5  |  1.595  |  DISEASES
115362  |  GBP5  |  1.594  |  DISEASES
2782  |  GNB1  |  1.294  |  DISEASES
2782  |  GNB1  |  1.294  |  DISEASES
7107  |  GPR137B  |  2.029  |  DISEASES
7107  |  GPR137B  |  2.028  |  DISEASES
3065  |  HDAC1  |  3.118  |  DISEASES
3065  |  HDAC1  |  3.118  |  DISEASES
3066  |  HDAC2  |  2.523  |  DISEASES
3066  |  HDAC2  |  2.523  |  DISEASES
10013  |  HDAC6  |  2.563  |  DISEASES
10013  |  HDAC6  |  2.562  |  DISEASES
55869  |  HDAC8  |  1.589  |  DISEASES
55869  |  HDAC8  |  1.589  |  DISEASES
9734  |  HDAC9  |  1.467  |  DISEASES
9734  |  HDAC9  |  1.467  |  DISEASES
51696  |  HECA  |  3.735  |  DISEASES
51696  |  HECA  |  3.735  |  DISEASES
391723  |  HELT  |  1.353  |  DISEASES
391723  |  HELT  |  1.352  |  DISEASES
3320  |  HSP90AA1  |  1.048  |  DISEASES
3320  |  HSP90AA1  |  1.048  |  DISEASES
3384  |  ICAM2  |  1.039  |  DISEASES
3384  |  ICAM2  |  1.039  |  DISEASES
3418  |  IDH2  |  2.017  |  DISEASES
3418  |  IDH2  |  2.016  |  DISEASES
3430  |  IFI35  |  1.34  |  DISEASES
3430  |  IFI35  |  1.339  |  DISEASES
3440  |  IFNA2  |  2.129  |  DISEASES
3440  |  IFNA2  |  2.129  |  DISEASES
147920  |  IGFL2  |  2.474  |  DISEASES
147920  |  IGFL2  |  2.474  |  DISEASES
3550  |  IK  |  1.05  |  DISEASES
3550  |  IK  |  1.05  |  DISEASES
22807  |  IKZF2  |  1.777  |  DISEASES
22807  |  IKZF2  |  1.776  |  DISEASES
3586  |  IL10  |  2.887  |  DISEASES
3586  |  IL10  |  2.887  |  DISEASES
3605  |  IL17A  |  1.851  |  DISEASES
3605  |  IL17A  |  1.851  |  DISEASES
112744  |  IL17F  |  2.306  |  DISEASES
112744  |  IL17F  |  2.305  |  DISEASES
3559  |  IL2RA  |  3.061  |  DISEASES
3559  |  IL2RA  |  3.061  |  DISEASES
3561  |  IL2RG  |  2.74  |  DISEASES
3561  |  IL2RG  |  2.739  |  DISEASES
386653  |  IL31  |  3.24  |  DISEASES
386653  |  IL31  |  3.239  |  DISEASES
133396  |  IL31RA  |  2.007  |  DISEASES
133396  |  IL31RA  |  2.006  |  DISEASES
9235  |  IL32  |  1.961  |  DISEASES
9235  |  IL32  |  1.961  |  DISEASES
55656  |  INTS8  |  1.498  |  DISEASES
55656  |  INTS8  |  1.497  |  DISEASES
3662  |  IRF4  |  2.646  |  DISEASES
3662  |  IRF4  |  2.645  |  DISEASES
3664  |  IRF6  |  4.045  |  DISEASES
3664  |  IRF6  |  4.044  |  DISEASES
3676  |  ITGA4  |  2.192  |  DISEASES
3676  |  ITGA4  |  2.192  |  DISEASES
3681  |  ITGAD  |  1.064  |  DISEASES
3681  |  ITGAD  |  1.063  |  DISEASES
3683  |  ITGAL  |  2.183  |  DISEASES
3683  |  ITGAL  |  2.183  |  DISEASES
3684  |  ITGAM  |  1.532  |  DISEASES
3684  |  ITGAM  |  1.531  |  DISEASES
3702  |  ITK  |  3.402  |  DISEASES
3702  |  ITK  |  3.401  |  DISEASES
3716  |  JAK1  |  1.706  |  DISEASES
3716  |  JAK1  |  1.706  |  DISEASES
3718  |  JAK3  |  3.647  |  DISEASES
3718  |  JAK3  |  3.647  |  DISEASES
56704  |  JPH1  |  1.01  |  DISEASES
56704  |  JPH1  |  1.01  |  DISEASES
131096  |  KCNH8  |  1.951  |  DISEASES
131096  |  KCNH8  |  1.95  |  DISEASES
3802  |  KIR2DL1  |  2.386  |  DISEASES
3802  |  KIR2DL1  |  2.386  |  DISEASES
3804  |  KIR2DL3  |  2.35  |  DISEASES
3804  |  KIR2DL3  |  2.349  |  DISEASES
3811  |  KIR3DL1  |  3.999  |  DISEASES
3811  |  KIR3DL1  |  3.999  |  DISEASES
3812  |  KIR3DL2  |  5.466  |  DISEASES
3812  |  KIR3DL2  |  5.466  |  DISEASES
3821  |  KLRC1  |  1.387  |  DISEASES
3821  |  KLRC1  |  1.386  |  DISEASES
3824  |  KLRD1  |  1.989  |  DISEASES
3824  |  KLRD1  |  1.989  |  DISEASES
54900  |  LAX1  |  2.163  |  DISEASES
54900  |  LAX1  |  2.163  |  DISEASES
3932  |  LCK  |  2.08  |  DISEASES
3932  |  LCK  |  2.08  |  DISEASES
4049  |  LTA  |  1.035  |  DISEASES
4049  |  LTA  |  1.035  |  DISEASES
84946  |  LTV1  |  1.61  |  DISEASES
84946  |  LTV1  |  1.609  |  DISEASES
51213  |  LUZP4  |  1.154  |  DISEASES
51213  |  LUZP4  |  1.153  |  DISEASES
4216  |  MAP3K4  |  1.157  |  DISEASES
4216  |  MAP3K4  |  1.157  |  DISEASES
4170  |  MCL1  |  1.289  |  DISEASES
4170  |  MCL1  |  1.289  |  DISEASES
2315  |  MLANA  |  1.154  |  DISEASES
2315  |  MLANA  |  1.153  |  DISEASES
4311  |  MME  |  3.918  |  DISEASES
4311  |  MME  |  3.917  |  DISEASES
4507  |  MTAP  |  2.064  |  DISEASES
4507  |  MTAP  |  2.063  |  DISEASES
10608  |  MXD4  |  1.156  |  DISEASES
10608  |  MXD4  |  1.155  |  DISEASES
4601  |  MXI1  |  1.52  |  DISEASES
4601  |  MXI1  |  1.519  |  DISEASES
4609  |  MYC  |  2.904  |  DISEASES
4609  |  MYC  |  2.903  |  DISEASES
26292  |  MYCBP  |  1.227  |  DISEASES
26292  |  MYCBP  |  1.226  |  DISEASES
89795  |  NAV3  |  3.743  |  DISEASES
89795  |  NAV3  |  3.743  |  DISEASES
9436  |  NCR2  |  1.11  |  DISEASES
9436  |  NCR2  |  1.109  |  DISEASES
64332  |  NFKBIZ  |  1.6  |  DISEASES
64332  |  NFKBIZ  |  1.6  |  DISEASES
4942  |  OAT  |  3.225  |  DISEASES
4942  |  OAT  |  3.224  |  DISEASES
56666  |  PANX2  |  1.04  |  DISEASES
56666  |  PANX2  |  1.039  |  DISEASES
142  |  PARP1  |  1.247  |  DISEASES
142  |  PARP1  |  1.246  |  DISEASES
5079  |  PAX5  |  3.044  |  DISEASES
5079  |  PAX5  |  3.043  |  DISEASES
5133  |  PDCD1  |  1.62  |  DISEASES
5133  |  PDCD1  |  1.619  |  DISEASES
9260  |  PDLIM7  |  2.422  |  DISEASES
9260  |  PDLIM7  |  2.421  |  DISEASES
5358  |  PLS3  |  4.529  |  DISEASES
5358  |  PLS3  |  4.528  |  DISEASES
5406  |  PNLIP  |  3.29  |  DISEASES
5406  |  PNLIP  |  3.29  |  DISEASES
4860  |  PNP  |  1.171  |  DISEASES
4860  |  PNP  |  1.171  |  DISEASES
5527  |  PPP2R5C  |  1.341  |  DISEASES
5527  |  PPP2R5C  |  1.341  |  DISEASES
5728  |  PTEN  |  1.408  |  DISEASES
5728  |  PTEN  |  1.408  |  DISEASES
5788  |  PTPRC  |  3.626  |  DISEASES
5788  |  PTPRC  |  3.625  |  DISEASES
5872  |  RAB13  |  1.316  |  DISEASES
5872  |  RAB13  |  1.315  |  DISEASES
5887  |  RAD23B  |  1.876  |  DISEASES
5887  |  RAD23B  |  1.875  |  DISEASES
387  |  RHOA  |  2.32  |  DISEASES
387  |  RHOA  |  2.319  |  DISEASES
63891  |  RNF123  |  1.724  |  DISEASES
63891  |  RNF123  |  1.723  |  DISEASES
9349  |  RPL23  |  1.27  |  DISEASES
9349  |  RPL23  |  1.27  |  DISEASES
6280  |  S100A9  |  2.276  |  DISEASES
6280  |  S100A9  |  2.276  |  DISEASES
6304  |  SATB1  |  2.366  |  DISEASES
6304  |  SATB1  |  2.366  |  DISEASES
6401  |  SELE  |  1.949  |  DISEASES
6401  |  SELE  |  1.948  |  DISEASES
259230  |  SGMS1  |  1.282  |  DISEASES
259230  |  SGMS1  |  1.281  |  DISEASES
8631  |  SKAP1  |  2.499  |  DISEASES
8631  |  SKAP1  |  2.498  |  DISEASES
347734  |  SLC35B2  |  2.479  |  DISEASES
347734  |  SLC35B2  |  2.478  |  DISEASES
23583  |  SMUG1  |  2.433  |  DISEASES
23583  |  SMUG1  |  2.433  |  DISEASES
100126781  |  SNAR-F  |  1.17  |  DISEASES
100126781  |  SNAR-F  |  1.17  |  DISEASES
692111  |  SNORD71  |  2.546  |  DISEASES
692111  |  SNORD71  |  2.545  |  DISEASES
6693  |  SPN  |  4.013  |  DISEASES
6693  |  SPN  |  4.012  |  DISEASES
23626  |  SPO11  |  1.201  |  DISEASES
23626  |  SPO11  |  1.201  |  DISEASES
6772  |  STAT1  |  1.815  |  DISEASES
6772  |  STAT1  |  1.814  |  DISEASES
6775  |  STAT4  |  2.824  |  DISEASES
6775  |  STAT4  |  2.824  |  DISEASES
6776  |  STAT5A  |  3.406  |  DISEASES
6776  |  STAT5A  |  3.406  |  DISEASES
6847  |  SYCP1  |  2.244  |  DISEASES
6847  |  SYCP1  |  2.243  |  DISEASES
6850  |  SYK  |  2.54  |  DISEASES
6850  |  SYK  |  2.539  |  DISEASES
6863  |  TAC1  |  1.363  |  DISEASES
6863  |  TAC1  |  1.362  |  DISEASES
54790  |  TET2  |  2.259  |  DISEASES
54790  |  TET2  |  2.258  |  DISEASES
7037  |  TFRC  |  1.67  |  DISEASES
7037  |  TFRC  |  1.67  |  DISEASES
387357  |  THEMIS  |  2.399  |  DISEASES
387357  |  THEMIS  |  2.398  |  DISEASES
7072  |  TIA1  |  5.393  |  DISEASES
7072  |  TIA1  |  5.392  |  DISEASES
51284  |  TLR7  |  1.537  |  DISEASES
51284  |  TLR7  |  1.537  |  DISEASES
54106  |  TLR9  |  1.485  |  DISEASES
54106  |  TLR9  |  1.484  |  DISEASES
253582  |  TMEM244  |  2.793  |  DISEASES
253582  |  TMEM244  |  2.793  |  DISEASES
7110  |  TMF1  |  3.578  |  DISEASES
7110  |  TMF1  |  3.578  |  DISEASES
7124  |  TNF  |  2.503  |  DISEASES
7124  |  TNF  |  2.502  |  DISEASES
8764  |  TNFRSF14  |  1.032  |  DISEASES
8764  |  TNFRSF14  |  1.032  |  DISEASES
7133  |  TNFRSF1B  |  1.367  |  DISEASES
7133  |  TNFRSF1B  |  1.367  |  DISEASES
7293  |  TNFRSF4  |  2.264  |  DISEASES
7293  |  TNFRSF4  |  2.264  |  DISEASES
9760  |  TOX  |  3.812  |  DISEASES
9760  |  TOX  |  3.812  |  DISEASES
58476  |  TP53INP2  |  1.153  |  DISEASES
58476  |  TP53INP2  |  1.152  |  DISEASES
80342  |  TRAF3IP3  |  2.303  |  DISEASES
80342  |  TRAF3IP3  |  2.303  |  DISEASES
55039  |  TRMT12  |  2.332  |  DISEASES
55039  |  TRMT12  |  2.332  |  DISEASES
80705  |  TSGA10  |  1.58  |  DISEASES
80705  |  TSGA10  |  1.579  |  DISEASES
200081  |  TXLNA  |  1.363  |  DISEASES
200081  |  TXLNA  |  1.362  |  DISEASES
7422  |  VEGFA  |  1.126  |  DISEASES
7422  |  VEGFA  |  1.125  |  DISEASES
2547  |  XRCC6  |  1.695  |  DISEASES
2547  |  XRCC6  |  1.695  |  DISEASES
8565  |  YARS  |  1.067  |  DISEASES
8565  |  YARS  |  1.066  |  DISEASES
29068  |  ZBTB44  |  1.124  |  DISEASES
29068  |  ZBTB44  |  1.123  |  DISEASES
340152  |  ZC3H12D  |  1.278  |  DISEASES
340152  |  ZC3H12D  |  1.277  |  DISEASES
7748  |  ZNF195  |  2.057  |  DISEASES
7748  |  ZNF195  |  2.057  |  DISEASES
Locus(Waiting for update.)
Disease ID 1397
Disease peripheral t-cell lymphoma
Integrated Phenotype(Waiting for update.)
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:23)
HP:0002665  |  Lymphoma  |  6
HP:0012190  |  T cell lymphoma  |  5
HP:0001888  |  Lymphocytopenia  |  2
HP:0009125  |  Lipodystrophy  |  2
HP:0002716  |  Lymph node hyperplasia  |  2
HP:0006554  |  Acute hepatic failure  |  1
HP:0012193  |  Anaplastic large-cell lymphoma  |  1
HP:0002326  |  TIA  |  1
HP:0009064  |  Generalized lipodystrophy  |  1
HP:0012539  |  Non-Hodgkin lymphoma  |  1
HP:0001399  |  Liver failure  |  1
HP:0000999  |  Pyoderma  |  1
HP:0100280  |  Morbus Crohn  |  1
HP:0000100  |  Nephrosis  |  1
HP:0002242  |  Enteropathy  |  1
HP:0011919  |  Pleural empyema  |  1
HP:0100008  |  Schwann cell tumour  |  1
HP:0011974  |  Myelofibrosis  |  1
HP:0005523  |  Lymphoproliferative disorder  |  1
HP:0002955  |  Granulomatosis  |  1
HP:0012189  |  Hodgkin disease  |  1
HP:0012156  |  Hemophagocytosis  |  1
HP:0002608  |  Celiac disease  |  1
Disease ID 1397
Disease peripheral t-cell lymphoma
Manually Symptom
UMLS  | Name(Total Manually Symptoms:4)
C0545080  |  composite lymphoma
C0162323  |  polyarthritis
C0079731  |  b cell lymphoma
C0031117  |  peripheral neuropathy
Text Mined Symptom(Waiting for update.)
Manually Genotype(Total Text Mining Genotypes:0)
(Waiting for update.)
Text Mining Genotype(Total Genotypes:0)
(Waiting for update.)
All Snps(Total Genotypes:3)
snpId pubmedId geneId geneSymbol diseaseId sourceId sentence score Year geneSymbol_dbSNP CHROMOSOME POS REF ALT
rs11348802224689848387RHOAumls:C0079774BeFreeThey include the V600E BRAF mutation in hairy cell leukemia, the L265P MYD88 mutation in Waldenström macroglobulinemia, the G17V RHOA mutation in angioimmunoblastic T-cell lymphoma and peripheral T-cell lymphoma, not otherwise specified, and the Y640F//D661Y/V/H/I//N647I STAT3 mutations in T-cell large granular lymphocytic leukemia.0.1208143262014BRAF7140753336AT,G,C
rs37189676024689848387RHOAumls:C0079774BeFreeThey include the V600E BRAF mutation in hairy cell leukemia, the L265P MYD88 mutation in Waldenström macroglobulinemia, the G17V RHOA mutation in angioimmunoblastic T-cell lymphoma and peripheral T-cell lymphoma, not otherwise specified, and the Y640F//D661Y/V/H/I//N647I STAT3 mutations in T-cell large granular lymphocytic leukemia.0.1208143262014ACAA1;MYD88338138714GT
rs38790727224689848387RHOAumls:C0079774BeFreeThey include the V600E BRAF mutation in hairy cell leukemia, the L265P MYD88 mutation in Waldenström macroglobulinemia, the G17V RHOA mutation in angioimmunoblastic T-cell lymphoma and peripheral T-cell lymphoma, not otherwise specified, and the Y640F//D661Y/V/H/I//N647I STAT3 mutations in T-cell large granular lymphocytic leukemia.0.1208143262014MYD88338141150TC
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 1397
Disease peripheral t-cell lymphoma
Case(Waiting for update.)