peripheral t-cell lymphoma |
Disease ID | 1397 |
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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) |
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 |
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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 |
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Disease | peripheral t-cell lymphoma |
Manually Symptom | UMLS | Name(Total Manually Symptoms:4) |
Text Mined Symptom | (Waiting for update.) |
Manually Genotype(Total Text Mining Genotypes:0) |
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(Waiting for update.) |
Text Mining Genotype(Total Genotypes:0) | |
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(Waiting for update.) |
All Snps(Total Genotypes:3) | |||||||||||||
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snpId | pubmedId | geneId | geneSymbol | diseaseId | sourceId | sentence | score | Year | geneSymbol_dbSNP | CHROMOSOME | POS | REF | ALT |
rs113488022 | 24689848 | 387 | RHOA | umls:C0079774 | BeFree | They 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. | 0.120814326 | 2014 | BRAF | 7 | 140753336 | A | T,G,C |
rs371896760 | 24689848 | 387 | RHOA | umls:C0079774 | BeFree | They 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. | 0.120814326 | 2014 | ACAA1;MYD88 | 3 | 38138714 | G | T |
rs387907272 | 24689848 | 387 | RHOA | umls:C0079774 | BeFree | They 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. | 0.120814326 | 2014 | MYD88 | 3 | 38141150 | T | C |
GWASdb Annotation(Total Genotypes:0) | |
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(Waiting for update.) |
GWASdb Snp Trait(Total Genotypes:0) | |
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(Waiting for update.) |
Mapped by lexical matching(Total Items:0) |
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(Waiting for update.) |
Mapped by homologous gene(Total Items:0) |
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(Waiting for update.) |
Disease ID | 1397 |
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Disease | peripheral t-cell lymphoma |
Case | (Waiting for update.) |