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PedAM

Pediatric Disease Annotations & Medicines



   acute leukemia
  

Disease ID 1497
Disease acute leukemia
Definition
leukemia in which the involved cell shows little or no differentiation, usually consisting of blast cells; two types are distinguished, acute lymphocytic and acute myelogenous leukemia.
Synonym
[m]acute leukaemia nos
[m]acute leukemia nos
acute leukaemia
acute leukaemia nos
acute leukaemia nos (disorder)
acute leukaemia, disease
acute leukaemia, morphology, including blast cell or undifferentiated leukaemia
acute leukaemias
acute leukemia nos
acute leukemia nos (disorder)
acute leukemia, disease
acute leukemia, disease (disorder)
acute leukemia, morphology, including blast cell or undifferentiated leukemia
acute leukemia, morphology, including blast cell or undifferentiated leukemia (morphologic abnormality)
acute leukemia, nos
acute leukemias
leukaemia acute
leukemia acute
leukemia of unspecified cell type, acute
leukemia, acute
DOID
UMLS
C0085669
SNOMED-CT
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:67)
C0023418  |  leukemia  |  8
C0027947  |  neutropenia  |  7
C0023470  |  myeloid leukemia  |  5
C0282193  |  iron overload  |  5
C0006840  |  candidiasis  |  5
C0040034  |  thrombocytopenia  |  4
C0023467  |  acute myeloid leukemia  |  4
C0040053  |  thrombosis  |  3
C1261473  |  sarcoma  |  3
C0003615  |  appendicitis  |  3
C0004030  |  aspergillosis  |  3
C0023449  |  acute lymphoblastic leukemia  |  2
C1568868  |  oral mucositis  |  2
C0152276  |  granulocytic sarcoma  |  2
C0035333  |  retinitis  |  2
C0026946  |  fungal disease  |  2
C0001125  |  lactic acidosis  |  2
C0085693  |  acute appendicitis  |  2
C0032285  |  pneumonia  |  2
C0343386  |  clostridium difficile infection  |  1
C0011570  |  depression  |  1
C1368107  |  bone marrow aplasia  |  1
C0003874  |  septic arthritis  |  1
C0004623  |  bacterial infections  |  1
C0035229  |  respiratory insufficiency  |  1
C0878544  |  cardiomyopathy  |  1
C0019829  |  hodgkin's lymphoma  |  1
C0035305  |  retinal detachment  |  1
C0017551  |  gilbert's syndrome  |  1
C0010414  |  cryptococcosis  |  1
C0019618  |  histiocytosis  |  1
C0026946  |  fungal infections  |  1
C0028754  |  obesity  |  1
C0019069  |  hemophilia  |  1
C0026946  |  fungal infection  |  1
C0023487  |  acute promyelocytic leukemia  |  1
C0014121  |  infective endocarditis  |  1
C0014118  |  endocarditis  |  1
C0001815  |  myelofibrosis  |  1
C0206686  |  adrenocortical carcinoma  |  1
C0024305  |  non-hodgkin lymphoma  |  1
C0036220  |  kaposi's sarcoma  |  1
C0012739  |  disseminated intravascular coagulation  |  1
C0003864  |  arthritis  |  1
C0027022  |  myeloproliferative disorders  |  1
C0031036  |  polyarteritis nodosa  |  1
C0024305  |  non-hodgkin's lymphoma  |  1
C0151744  |  myocardial ischemia  |  1
C0040128  |  thyroid disease  |  1
C0012739  |  consumption coagulopathy  |  1
C0376545  |  hematologic malignancy  |  1
C0019621  |  langerhans cell histiocytosis  |  1
C0376545  |  hematologic malignancies  |  1
C0035305  |  retinal detachments  |  1
C0030312  |  bone marrow failure  |  1
C0376545  |  hematological malignancy  |  1
C0004623  |  bacterial infection  |  1
C0026985  |  myelodysplasia  |  1
C0035412  |  rhabdomyosarcoma  |  1
C0085273  |  parvovirus b19 infection  |  1
C0027022  |  myeloproliferative disorder  |  1
C0006142  |  breast cancer  |  1
C0042769  |  virus infection  |  1
C0022116  |  ischemia  |  1
C0206178  |  cmv retinitis  |  1
C0023473  |  chronic myeloid leukemia  |  1
C0009319  |  colitis  |  1
Curated Gene(Waiting for update.)
Inferring Gene
Entrez_id | Symbol | Resource(Total Genes:1)
4524  |  MTHFR  |  infer
Text Mined Gene
Entrez_id | Symbol | Score | Resource(Total Genes:509)
100506492  |  DSCAM-AS1  |  DISEASES
102725541  |  ELDR  |  DISEASES
928  |  CD9  |  DISEASES
920  |  CD4  |  DISEASES
55359  |  STYK1  |  DISEASES
933  |  CD22  |  DISEASES
10077  |  TSPAN32  |  DISEASES
8079  |  MLF2  |  DISEASES
7066  |  THPO  |  DISEASES
1053  |  CEBPE  |  DISEASES
51382  |  ATP6V1D  |  DISEASES
5834  |  PYGB  |  DISEASES
10273  |  STUB1  |  DISEASES
56915  |  EXOSC5  |  DISEASES
1891  |  ECH1  |  DISEASES
973  |  CD79A  |  DISEASES
1628  |  DBP  |  DISEASES
2057  |  EPOR  |  DISEASES
3202  |  HOXA5  |  DISEASES
1577  |  CYP3A5  |  DISEASES
51510  |  CHMP5  |  DISEASES
7431  |  VIM  |  DISEASES
4353  |  MPO  |  DISEASES
1440  |  CSF3  |  DISEASES
708  |  C1QBP  |  DISEASES
29098  |  RANGRF  |  DISEASES
952  |  CD38  |  DISEASES
3558  |  IL2  |  DISEASES
6688  |  SPI1  |  DISEASES
595  |  CCND1  |  DISEASES
329  |  BIRC2  |  DISEASES
4254  |  KITLG  |  DISEASES
1027  |  CDKN1B  |  DISEASES
55507  |  GPRC5D  |  DISEASES
3458  |  IFNG  |  DISEASES
2597  |  GAPDH  |  DISEASES
26127  |  FGFR1OP2  |  DISEASES
80329  |  ULBP1  |  DISEASES
6534  |  SLC6A7  |  DISEASES
1007  |  CDH9  |  DISEASES
3565  |  IL4  |  DISEASES
5917  |  RARS  |  DISEASES
3485  |  IGFBP2  |  DISEASES
7799  |  PRDM2  |  DISEASES
6402  |  SELL  |  DISEASES
9429  |  ABCG2  |  DISEASES
22936  |  ELL2  |  DISEASES
11064  |  CNTRL  |  DISEASES
84955  |  NUDCD1  |  DISEASES
8743  |  TNFSF10  |  DISEASES
2322  |  FLT3  |  DISEASES
3204  |  HOXA7  |  DISEASES
1026  |  CDKN1A  |  DISEASES
51081  |  MRPS7  |  DISEASES
84081  |  NSRP1  |  DISEASES
7429  |  VIL1  |  DISEASES
3315  |  HSPB1  |  DISEASES
2952  |  GSTT1  |  DISEASES
968  |  CD68  |  DISEASES
9910  |  RABGAP1L  |  DISEASES
4298  |  MLLT1  |  DISEASES
2056  |  EPO  |  DISEASES
57688  |  ZSWIM6  |  DISEASES
5914  |  RARA  |  DISEASES
113  |  ADCY7  |  DISEASES
60678  |  EEFSEC  |  DISEASES
182  |  JAG1  |  DISEASES
1401  |  CRP  |  DISEASES
10752  |  CHL1  |  DISEASES
26519  |  TIMM10  |  DISEASES
5156  |  PDGFRA  |  DISEASES
80761  |  UPK3B  |  DISEASES
4005  |  LMO2  |  DISEASES
1019  |  CDK4  |  DISEASES
23416  |  KCNH3  |  DISEASES
3431  |  SP110  |  DISEASES
3569  |  IL6  |  DISEASES
55363  |  HEMGN  |  DISEASES
971  |  CD72  |  DISEASES
7274  |  TTPA  |  DISEASES
8836  |  GGH  |  DISEASES
53826  |  FXYD6  |  DISEASES
10113  |  PREB  |  DISEASES
3417  |  IDH1  |  DISEASES
4069  |  LYZ  |  DISEASES
29121  |  CLEC2D  |  DISEASES
51646  |  YPEL5  |  DISEASES
7450  |  VWF  |  DISEASES
5159  |  PDGFRB  |  DISEASES
3690  |  ITGB3  |  DISEASES
9172  |  MYOM2  |  DISEASES
945  |  CD33  |  DISEASES
1387  |  CREBBP  |  DISEASES
23090  |  ZNF423  |  DISEASES
3674  |  ITGA2B  |  DISEASES
9135  |  RABEP1  |  DISEASES
23361  |  ZNF629  |  DISEASES
7011  |  TEP1  |  DISEASES
8178  |  ELL  |  DISEASES
57148  |  RALGAPB  |  DISEASES
6929  |  TCF3  |  DISEASES
6598  |  SMARCB1  |  DISEASES
2033  |  EP300  |  DISEASES
23476  |  BRD4  |  DISEASES
1991  |  ELANE  |  DISEASES
3574  |  IL7  |  DISEASES
3791  |  KDR  |  DISEASES
943  |  TNFRSF8  |  DISEASES
867  |  CBL  |  DISEASES
60482  |  SLC5A7  |  DISEASES
5471  |  PPAT  |  DISEASES
941  |  CD80  |  DISEASES
2247  |  FGF2  |  DISEASES
55081  |  IFT57  |  DISEASES
3589  |  IL11  |  DISEASES
7067  |  THRA  |  DISEASES
2122  |  MECOM  |  DISEASES
5443  |  POMC  |  DISEASES
1788  |  DNMT3A  |  DISEASES
4066  |  LYL1  |  DISEASES
3383  |  ICAM1  |  DISEASES
51265  |  CDKL3  |  DISEASES
6722  |  SRF  |  DISEASES
8829  |  NRP1  |  DISEASES
7994  |  KAT6A  |  DISEASES
5243  |  ABCB1  |  DISEASES
84920  |  ALG10  |  DISEASES
1017  |  CDK2  |  DISEASES
5371  |  PML  |  DISEASES
3687  |  ITGAX  |  DISEASES
863  |  CBFA2T3  |  DISEASES
9611  |  NCOR1  |  DISEASES
7157  |  TP53  |  DISEASES
6455  |  SH3GL1  |  DISEASES
150094  |  SIK1  |  DISEASES
207  |  AKT1  |  DISEASES
23126  |  POGZ  |  DISEASES
6233  |  RPS27A  |  DISEASES
4211  |  MEIS1  |  DISEASES
8994  |  LIMD1  |  DISEASES
64434  |  NOM1  |  DISEASES
8795  |  TNFRSF10B  |  DISEASES
7013  |  TERF1  |  DISEASES
1030  |  CDKN2B  |  DISEASES
3439  |  IFNA1  |  DISEASES
4851  |  NOTCH1  |  DISEASES
472  |  ATM  |  DISEASES
3176  |  HNMT  |  DISEASES
2241  |  FER  |  DISEASES
7082  |  TJP1  |  DISEASES
678  |  ZFP36L2  |  DISEASES
2321  |  FLT1  |  DISEASES
8467  |  SMARCA5  |  DISEASES
10225  |  CD96  |  DISEASES
925  |  CD8A  |  DISEASES
7070  |  THY1  |  DISEASES
760  |  CA2  |  DISEASES
1436  |  CSF1R  |  DISEASES
1633  |  DCK  |  DISEASES
27163  |  NAAA  |  DISEASES
5097  |  PCDH1  |  DISEASES
3815  |  KIT  |  DISEASES
6781  |  STC1  |  DISEASES
84303  |  CHCHD6  |  DISEASES
23547  |  LILRA4  |  DISEASES
84449  |  ZNF333  |  DISEASES
9794  |  MAML1  |  DISEASES
6777  |  STAT5B  |  DISEASES
6886  |  TAL1  |  DISEASES
7412  |  VCAM1  |  DISEASES
2215  |  FCGR3B  |  DISEASES
824  |  CAPN2  |  DISEASES
2487  |  FRZB  |  DISEASES
27306  |  HPGDS  |  DISEASES
3490  |  IGFBP7  |  DISEASES
213  |  ALB  |  DISEASES
308  |  ANXA5  |  DISEASES
3562  |  IL3  |  DISEASES
1437  |  CSF2  |  DISEASES
30012  |  TLX3  |  DISEASES
4869  |  NPM1  |  DISEASES
54882  |  ANKHD1  |  DISEASES
122769  |  LRR1  |  DISEASES
3251  |  HPRT1  |  DISEASES
290  |  ANPEP  |  DISEASES
63928  |  CHP2  |  DISEASES
861  |  RUNX1  |  DISEASES
84798  |  C19orf48  |  DISEASES
2125  |  EVPL  |  DISEASES
84132  |  USP42  |  DISEASES
9081  |  PRY  |  DISEASES
598  |  BCL2L1  |  DISEASES
116984  |  ARAP2  |  DISEASES
3308  |  HSPA4  |  DISEASES
10251  |  SPRY3  |  DISEASES
3689  |  ITGB2  |  DISEASES
442862  |  PRY2  |  DISEASES
613  |  BCR  |  DISEASES
442866  |  PRYP4  |  DISEASES
2815  |  GP9  |  DISEASES
171558  |  PTCRA  |  DISEASES
4330  |  MN1  |  DISEASES
8019  |  BRD3  |  DISEASES
8028  |  MLLT10  |  DISEASES
54205  |  CYCS  |  DISEASES
27087  |  B3GAT1  |  DISEASES
2147  |  F2  |  DISEASES
5778  |  PTPN7  |  DISEASES
55695  |  NSUN5  |  DISEASES
9134  |  CCNE2  |  DISEASES
7015  |  TERT  |  DISEASES
3265  |  HRAS  |  DISEASES
947  |  CD34  |  DISEASES
9344  |  TAOK2  |  DISEASES
144245  |  ALG10B  |  DISEASES
56675  |  NRIP3  |  DISEASES
836  |  CASP3  |  DISEASES
2944  |  GSTM1  |  DISEASES
924  |  CD7  |  DISEASES
84883  |  AIFM2  |  DISEASES
8837  |  CFLAR  |  DISEASES
79870  |  BAALC  |  DISEASES
5591  |  PRKDC  |  DISEASES
653499  |  LGALS7B  |  DISEASES
80818  |  ZNF436  |  DISEASES
25758  |  KIAA1549L  |  DISEASES
57453  |  DSCAML1  |  DISEASES
7298  |  TYMS  |  DISEASES
901  |  CCNG2  |  DISEASES
140545  |  RNF32  |  DISEASES
4928  |  NUP98  |  DISEASES
1604  |  CD55  |  DISEASES
4302  |  MLLT6  |  DISEASES
93185  |  IGSF8  |  DISEASES
5306  |  PITPNA  |  DISEASES
2824  |  GPM6B  |  DISEASES
4684  |  NCAM1  |  DISEASES
1728  |  NQO1  |  DISEASES
2146  |  EZH2  |  DISEASES
811  |  CALR  |  DISEASES
9920  |  KBTBD11  |  DISEASES
5345  |  SERPINF2  |  DISEASES
9203  |  ZMYM3  |  DISEASES
113878  |  DTX2  |  DISEASES
1879  |  EBF1  |  DISEASES
9202  |  ZMYM4  |  DISEASES
1555  |  CYP2B6  |  DISEASES
148266  |  ZNF569  |  DISEASES
114971  |  PTPMT1  |  DISEASES
1435  |  CSF1  |  DISEASES
80789  |  INTS5  |  DISEASES
3563  |  IL3RA  |  DISEASES
1789  |  DNMT3B  |  DISEASES
219621  |  C10orf107  |  DISEASES
201501  |  ZBTB7C  |  DISEASES
10614  |  HEXIM1  |  DISEASES
3214  |  HOXB4  |  DISEASES
84295  |  PHF6  |  DISEASES
2811  |  GP1BA  |  DISEASES
842  |  CASP9  |  DISEASES
6938  |  TCF12  |  DISEASES
9146  |  HGS  |  DISEASES
7490  |  WT1  |  DISEASES
56001  |  NXF2  |  DISEASES
10320  |  IKZF1  |  DISEASES
6401  |  SELE  |  DISEASES
796  |  CALCA  |  DISEASES
3418  |  IDH2  |  DISEASES
25901  |  CCDC28A  |  DISEASES
9899  |  SV2B  |  DISEASES
7181  |  NR2C1  |  DISEASES
2152  |  F3  |  DISEASES
55693  |  KDM4D  |  DISEASES
6887  |  TAL2  |  DISEASES
3320  |  HSP90AA1  |  DISEASES
81608  |  FIP1L1  |  DISEASES
1032  |  CDKN2D  |  DISEASES
9138  |  ARHGEF1  |  DISEASES
55146  |  ZDHHC4  |  DISEASES
3932  |  LCK  |  DISEASES
7704  |  ZBTB16  |  DISEASES
23236  |  PLCB1  |  DISEASES
4004  |  LMO1  |  DISEASES
6622  |  SNCA  |  DISEASES
203068  |  TUBB  |  DISEASES
5329  |  PLAUR  |  DISEASES
22978  |  NT5C2  |  DISEASES
4602  |  MYB  |  DISEASES
9516  |  LITAF  |  DISEASES
966  |  CD59  |  DISEASES
5781  |  PTPN11  |  DISEASES
6776  |  STAT5A  |  DISEASES
27255  |  CNTN6  |  DISEASES
442865  |  PRYP3  |  DISEASES
921  |  CD5  |  DISEASES
864  |  RUNX3  |  DISEASES
3205  |  HOXA9  |  DISEASES
53827  |  FXYD5  |  DISEASES
1499  |  CTNNB1  |  DISEASES
10019  |  SH2B3  |  DISEASES
2624  |  GATA2  |  DISEASES
3767  |  KCNJ11  |  DISEASES
2879  |  GPX4  |  DISEASES
1399  |  CRKL  |  DISEASES
57591  |  MKL1  |  DISEASES
331  |  XIAP  |  DISEASES
355  |  FAS  |  DISEASES
56164  |  STK31  |  DISEASES
140885  |  SIRPA  |  DISEASES
51710  |  ZNF44  |  DISEASES
54892  |  NCAPG2  |  DISEASES
10425  |  ARIH2  |  DISEASES
3899  |  AFF3  |  DISEASES
6288  |  SAA1  |  DISEASES
3683  |  ITGAL  |  DISEASES
85236  |  HIST1H2BK  |  DISEASES
5625  |  PRODH  |  DISEASES
9204  |  ZMYM6  |  DISEASES
135250  |  RAET1E  |  DISEASES
64919  |  BCL11B  |  DISEASES
60  |  ACTB  |  DISEASES
9961  |  MVP  |  DISEASES
1612  |  DAPK1  |  DISEASES
5079  |  PAX5  |  DISEASES
6714  |  SRC  |  DISEASES
4763  |  NF1  |  DISEASES
841  |  CASP8  |  DISEASES
11091  |  WDR5  |  DISEASES
2526  |  FUT4  |  DISEASES
3821  |  KLRC1  |  DISEASES
1786  |  DNMT1  |  DISEASES
6427  |  SRSF2  |  DISEASES
7037  |  TFRC  |  DISEASES
6693  |  SPN  |  DISEASES
2114  |  ETS2  |  DISEASES
3135  |  HLA-G  |  DISEASES
170482  |  CLEC4C  |  DISEASES
25942  |  SIN3A  |  DISEASES
4311  |  MME  |  DISEASES
2993  |  GYPA  |  DISEASES
10848  |  PPP1R13L  |  DISEASES
7150  |  TOP1  |  DISEASES
2475  |  MTOR  |  DISEASES
916  |  CD3E  |  DISEASES
171017  |  ZNF384  |  DISEASES
1639  |  DCTN1  |  DISEASES
23038  |  WDTC1  |  DISEASES
142  |  PARP1  |  DISEASES
11116  |  FGFR1OP  |  DISEASES
3664  |  IRF6  |  DISEASES
1378  |  CR1  |  DISEASES
1380  |  CR2  |  DISEASES
7139  |  TNNT2  |  DISEASES
5788  |  PTPRC  |  DISEASES
64407  |  RGS18  |  DISEASES
51278  |  IER5  |  DISEASES
462  |  SERPINC1  |  DISEASES
356  |  FASLG  |  DISEASES
2214  |  FCGR3A  |  DISEASES
10962  |  MLLT11  |  DISEASES
8528  |  DDO  |  DISEASES
4170  |  MCL1  |  DISEASES
55278  |  QRSL1  |  DISEASES
2209  |  FCGR1A  |  DISEASES
8515  |  ITGA10  |  DISEASES
914  |  CD2  |  DISEASES
965  |  CD58  |  DISEASES
4893  |  NRAS  |  DISEASES
10660  |  LBX1  |  DISEASES
3195  |  TLX1  |  DISEASES
3149  |  HMGB3  |  DISEASES
959  |  CD40LG  |  DISEASES
728911  |  CT45A2  |  DISEASES
5688  |  PSMA7  |  DISEASES
5236  |  PGM1  |  DISEASES
1791  |  DNTT  |  DISEASES
3725  |  JUN  |  DISEASES
860  |  RUNX2  |  DISEASES
8813  |  DPM1  |  DISEASES
2060  |  EPS15  |  DISEASES
5728  |  PTEN  |  DISEASES
7422  |  VEGFA  |  DISEASES
2889  |  RAPGEF1  |  DISEASES
25  |  ABL1  |  DISEASES
4352  |  MPL  |  DISEASES
728343  |  NXF2B  |  DISEASES
1441  |  CSF3R  |  DISEASES
1046  |  CDX4  |  DISEASES
1043  |  CD52  |  DISEASES
6891  |  TAP2  |  DISEASES
978  |  CDA  |  DISEASES
171023  |  ASXL1  |  DISEASES
22852  |  ANKRD26  |  DISEASES
3107  |  HLA-C  |  DISEASES
11040  |  PIM2  |  DISEASES
4524  |  MTHFR  |  DISEASES
3133  |  HLA-E  |  DISEASES
648  |  BMI1  |  DISEASES
2623  |  GATA1  |  DISEASES
5611  |  DNAJC3  |  DISEASES
3105  |  HLA-A  |  DISEASES
7056  |  THBD  |  DISEASES
4609  |  MYC  |  DISEASES
127262  |  TPRG1L  |  DISEASES
3963  |  LGALS7  |  DISEASES
3400  |  ID4  |  DISEASES
1543  |  CYP1A1  |  DISEASES
54790  |  TET2  |  DISEASES
5931  |  RBBP7  |  DISEASES
3440  |  IFNA2  |  DISEASES
4300  |  MLLT3  |  DISEASES
7280  |  TUBB2A  |  DISEASES
284390  |  ZNF763  |  DISEASES
5277  |  PIGA  |  DISEASES
11168  |  PSIP1  |  DISEASES
414  |  ARSD  |  DISEASES
29126  |  CD274  |  DISEASES
3717  |  JAK2  |  DISEASES
83650  |  SLC35G5  |  DISEASES
7750  |  ZMYM2  |  DISEASES
9811  |  CTIF  |  DISEASES
7862  |  BRPF1  |  DISEASES
6419  |  SETMAR  |  DISEASES
56254  |  RNF20  |  DISEASES
6003  |  RGS13  |  DISEASES
3239  |  HOXD13  |  DISEASES
2113  |  ETS1  |  DISEASES
114609  |  TIRAP  |  DISEASES
23041  |  MON2  |  DISEASES
4299  |  AFF1  |  DISEASES
6046  |  BRD2  |  DISEASES
6387  |  CXCL12  |  DISEASES
115560  |  ZNF501  |  DISEASES
4629  |  MYH11  |  DISEASES
2120  |  ETV6  |  DISEASES
116135  |  LRRC3B  |  DISEASES
85403  |  EAF1  |  DISEASES
7913  |  DEK  |  DISEASES
5609  |  MAP2K7  |  DISEASES
2950  |  GSTP1  |  DISEASES
84444  |  DOT1L  |  DISEASES
23532  |  PRAME  |  DISEASES
4363  |  ABCC1  |  DISEASES
4839  |  NOP2  |  DISEASES
23028  |  KDM1A  |  DISEASES
55536  |  CDCA7L  |  DISEASES
23160  |  WDR43  |  DISEASES
340273  |  ABCB5  |  DISEASES
9699  |  RIMS2  |  DISEASES
7018  |  TF  |  DISEASES
50489  |  CD207  |  DISEASES
7852  |  CXCR4  |  DISEASES
9354  |  UBE4A  |  DISEASES
1385  |  CREB1  |  DISEASES
1111  |  CHEK1  |  DISEASES
8925  |  HERC1  |  DISEASES
55743  |  CHFR  |  DISEASES
8861  |  LDB1  |  DISEASES
2260  |  FGFR1  |  DISEASES
57448  |  BIRC6  |  DISEASES
1029  |  CDKN2A  |  DISEASES
7155  |  TOP2B  |  DISEASES
56616  |  DIABLO  |  DISEASES
960  |  CD44  |  DISEASES
7124  |  TNF  |  DISEASES
10499  |  NCOA2  |  DISEASES
7465  |  WEE1  |  DISEASES
862  |  RUNX1T1  |  DISEASES
5087  |  PBX1  |  DISEASES
3276  |  PRMT1  |  DISEASES
84106  |  PRAM1  |  DISEASES
196527  |  ANO6  |  DISEASES
3925  |  STMN1  |  DISEASES
7153  |  TOP2A  |  DISEASES
3586  |  IL10  |  DISEASES
10043  |  TOM1  |  DISEASES
54838  |  WBP1L  |  DISEASES
8842  |  PROM1  |  DISEASES
1849  |  DUSP7  |  DISEASES
4193  |  MDM2  |  DISEASES
30816  |  ERVW-1  |  DISEASES
4345  |  CD200  |  DISEASES
5238  |  PGM3  |  DISEASES
1050  |  CEBPA  |  DISEASES
27  |  ABL2  |  DISEASES
2994  |  GYPB  |  DISEASES
2053  |  EPHX2  |  DISEASES
404635  |  NANOGP1  |  DISEASES
399687  |  MYO18A  |  DISEASES
930  |  CD19  |  DISEASES
5134  |  PDCD2  |  DISEASES
8615  |  USO1  |  DISEASES
3684  |  ITGAM  |  DISEASES
26150  |  RIBC2  |  DISEASES
3227  |  HOXC11  |  DISEASES
317  |  APAF1  |  DISEASES
567  |  B2M  |  DISEASES
4927  |  NUP88  |  DISEASES
81033  |  KCNH6  |  DISEASES
9212  |  AURKB  |  DISEASES
115727  |  RASGRP4  |  DISEASES
8148  |  TAF15  |  DISEASES
7409  |  VAV1  |  DISEASES
348120  |  LINC01193  |  DISEASES
285758  |  LINC01268  |  DISEASES
103164619  |  PCAT2  |  DISEASES
100126781  |  SNAR-F  |  DISEASES
692215  |  SNORD112  |  DISEASES
26769  |  SNORD81  |  DISEASES
Locus(Waiting for update.)
Disease ID 1497
Disease acute leukemia
Integrated Phenotype(Waiting for update.)
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:63)
HP:0001909  |  Leukemia  |  8
HP:0001875  |  Neutropenia  |  7
HP:0012324  |  Myeloid leukemia  |  5
HP:0001873  |  Low platelet count  |  4
HP:0004808  |  Acute myelogenous leukemia  |  4
HP:0001907  |  Thromboembolic disease  |  3
HP:0002664  |  Neoplasia  |  3
HP:0100242  |  Sarcoma  |  3
HP:0100806  |  Sepsis  |  3
HP:0001945  |  Fever  |  3
HP:0001974  |  Leukocytosis  |  2
HP:0001941  |  acidemia  |  2
HP:0002090  |  Pneumonia  |  2
HP:0006721  |  Acute lymphocytic leukemia  |  2
HP:0030731  |  Carcinoma  |  2
HP:0002835  |  Aspiration  |  2
HP:0003128  |  Lactic acidosis  |  2
HP:0002653  |  Bone pain  |  1
HP:0004387  |  Enterocolitis  |  1
HP:0001513  |  Obesity  |  1
HP:0004900  |  Severe lactic acidosis  |  1
HP:0003002  |  Breast carcinoma  |  1
HP:0002625  |  Blood clot in a deep vein  |  1
HP:0001908  |  Hypoplastic anemia  |  1
HP:0012539  |  Non-Hodgkin lymphoma  |  1
HP:0000105  |  Renal enlargement  |  1
HP:0011974  |  Myelofibrosis  |  1
HP:0012531  |  Pain  |  1
HP:0005521  |  Disseminated intravascular coagulation  |  1
HP:0002716  |  Lymph node hyperplasia  |  1
HP:0003095  |  Septic arthritis  |  1
HP:0006744  |  Adrenal carcinoma  |  1
HP:0100584  |  Endocarditis  |  1
HP:0001638  |  Cardiomyopathy  |  1
HP:0001433  |  Enlarged liver and spleen  |  1
HP:0005528  |  Bone marrow hypoplasia  |  1
HP:0003256  |  Coagulopathy  |  1
HP:0000365  |  Hearing impairment  |  1
HP:0002113  |  Pulmonary infiltrates  |  1
HP:0004936  |  Blood clot in vein  |  1
HP:0000820  |  Thyroid abnormality  |  1
HP:0100726  |  Kaposi's sarcoma  |  1
HP:0001250  |  Seizures  |  1
HP:0002202  |  Pleural effusion  |  1
HP:0012132  |  Erythroid hyperplasia  |  1
HP:0000541  |  Detached retina  |  1
HP:0012189  |  Hodgkin disease  |  1
HP:0004836  |  Acute promyelocytic leukemia  |  1
HP:0100727  |  Histiocytosis  |  1
HP:0000716  |  Depression  |  1
HP:0002859  |  Rhabdomyosarcoma  |  1
HP:0001824  |  Weight loss  |  1
HP:0002863  |  Myelodysplastic syndrome  |  1
HP:0002315  |  Headaches  |  1
HP:0005506  |  Chronic myeloid leukemia  |  1
HP:0006689  |  Bacterial endocarditis  |  1
HP:0002170  |  Intracranial hemorrhage  |  1
HP:0005547  |  Myeloproliferative disorder  |  1
HP:0002583  |  Colitis  |  1
HP:0002955  |  Granulomatosis  |  1
HP:0002093  |  progressive respiratory failure  |  1
HP:0010447  |  Fistula in ano  |  1
HP:0001369  |  Arthritis  |  1
Disease ID 1497
Disease acute leukemia
Manually Symptom(Waiting for update.)
Text Mined Symptom
UMLS | Name | Sentences' Count(Total Symptoms:46)
C0009450  |  infection  |  20
C0021311  |  infections  |  9
C1839611  |  n syndrome  |  7
C0027947  |  neutropenia  |  7
C0006840  |  candidiasis  |  5
C0040034  |  thrombocytopenia  |  4
C0040038  |  thromboembolism  |  3
C0746883  |  febrile neutropenia  |  3
C0004030  |  aspergillosis  |  3
C0015967  |  fever  |  3
C0003615  |  appendicitis  |  3
C0036690  |  sepsis  |  3
C0040053  |  thrombosis  |  3
C0948150  |  splenic candidiasis  |  2
C0001125  |  lactic acidosis  |  2
C0343885  |  chronic disseminated candidiasis  |  2
C0085693  |  acute appendicitis  |  2
C0032285  |  pneumonia  |  2
C0948689  |  hepatosplenic candidiasis  |  2
C1568868  |  oral mucositis  |  2
C0153252  |  disseminated candidiasis  |  2
C0004623  |  bacterial infections  |  1
C0012739  |  consumption coagulopathy  |  1
C0042487  |  venous thrombosis  |  1
C0005779  |  coagulopathy  |  1
C0012739  |  disseminated intravascular coagulation  |  1
C0085274  |  parvovirus b19  |  1
C0014121  |  infective endocarditis  |  1
C0029166  |  oral manifestations  |  1
C0036220  |  kaposi's sarcoma  |  1
C0235896  |  pulmonary infiltrates  |  1
C0746883  |  neutropenic fever  |  1
C0085082  |  fungemia  |  1
C0205851  |  germ cell tumor  |  1
C0343386  |  clostridium difficile infection  |  1
C0011570  |  depression  |  1
C0041364  |  tumor lysis syndrome  |  1
C0026946  |  fungal infection  |  1
C0343387  |  neutropenic enterocolitis  |  1
C0085273  |  parvovirus b19 infection  |  1
C0036690  |  septicemia  |  1
C0003864  |  arthritis  |  1
C0035229  |  respiratory insufficiency  |  1
C0014118  |  endocarditis  |  1
C0042769  |  virus infection  |  1
C0162679  |  leukemic infiltration  |  1
Manually Genotype(Total Text Mining Genotypes:0)
(Waiting for update.)
All Snps(Total Genotypes:18)
snpId pubmedId geneId geneSymbol diseaseId sourceId sentence score Year geneSymbol_dbSNP CHROMOSOME POS REF ALT
rs1045642211336255243ABCB1umls:C0085669BeFreeAssociation of an MDR1 gene (C3435T) polymorphism with acute leukemia in India.0.0078718142010ABCB1787509329AT,G
rs1048943230565461543CYP1A1umls:C0085669BeFreeAssociation between CYP1A1 Ile462Val variation and acute leukemia risk: meta-analyses including 2164 cases and 4160 controls.0.0010857672012CYP1A11574720644TG,C,A
rs1137101170720673953LEPRumls:C0085669BeFreeThe aim of the study was to evaluate bone marrow and peripheral blood leptin level and frequency of distribution of leptin receptor gene polymorphism Gln223Arg in children with acute leukemia.0.0005428842006LEPR165592830AG
rs1137101170720673952LEPumls:C0085669BeFreeThe aim of the study was to evaluate bone marrow and peripheral blood leptin level and frequency of distribution of leptin receptor gene polymorphism Gln223Arg in children with acute leukemia.0.0005428842006LEPR165592830AG
rs12143459218392055207AKT1umls:C0085669BeFreeMutational analysis of oncogenic AKT E17K mutation in common solid cancers and acute leukaemias.0.0010857672008AKT114104780214CT
rs121918464219307665781PTPN11umls:C0085669BeFreeThus, Ptpn11(E76K) mutation has non-lineage-specific effects on malignant transformation of hematopoietic cells and initiates acute leukemias at various stages of hematopoiesis.0.0008143262011PTPN1112112450406GA,C
rs13181244865062068ERCC2umls:C0085669BeFreeThe effect of XPD/ERCC2 Lys751Gln polymorphism on acute leukemia risk: a systematic review and meta-analysis.0.0005428842014ERCC2;KLC31945351661TA,G
rs1800566229768395444PON1umls:C0085669BeFreeNQO1 rs1800566 (C609T), PON1 rs662 (Q192R), and PON1 rs854560 (L55M) polymorphisms segregate the risk of childhood acute leukemias according to age range distribution.0.0002714422012NQO11669711242GA
rs38660211822652301627BDNFumls:C0085669BeFreeThe BDNF Val66Met polymorphism may contribute to development of depressive symptomatology in patients undergoing stressful life events, such as diagnosis of acute leukemia and preparation for HSCT.0.0005428842012NANANANANA
rs386626619214215403717JAK2umls:C0085669BeFreeThe transformation of MPNs into acute leukemia is by itself a very rare phenomenon, and so is the persistence of the JAK2(V617F) mutation after blast crisis.0.0035287442011NANANANANA
rs386626619216586593717JAK2umls:C0085669BeFreeJAK2 V617F mutation was detected after transformation to CMML in 1 of them; in the other, a novel translocation t(5;12)(p13;q24) was observed at the time of progression to acute leukemia.0.0035287442011NANANANANA
rs386626619228188583717JAK2umls:C0085669BeFreeA high JAK2(V617F) allele burden was correlated with the transformation to myelofibrosis (p<0.0001), but not with the transformation to acute leukemia.0.0035287442012NANANANANA
rs397507444179700894524MTHFRumls:C0085669BeFreeThe MTHFR C677T and A1298C polymorphisms are not significant risk factors in adult acute leukemia in the Korean population.0.0053528932007MTHFR111794407TG
rs662229768395444PON1umls:C0085669BeFreeNQO1 rs1800566 (C609T), PON1 rs662 (Q192R), and PON1 rs854560 (L55M) polymorphisms segregate the risk of childhood acute leukemias according to age range distribution.0.0002714422012PON1795308134TC
rs77375493216586593717JAK2umls:C0085669BeFreeJAK2 V617F mutation was detected after transformation to CMML in 1 of them; in the other, a novel translocation t(5;12)(p13;q24) was observed at the time of progression to acute leukemia.0.0035287442011JAK2;INSL695073770GA,T
rs77375493214215403717JAK2umls:C0085669BeFreeThe transformation of MPNs into acute leukemia is by itself a very rare phenomenon, and so is the persistence of the JAK2(V617F) mutation after blast crisis.0.0035287442011JAK2;INSL695073770GA,T
rs77375493228188583717JAK2umls:C0085669BeFreeA high JAK2(V617F) allele burden was correlated with the transformation to myelofibrosis (p<0.0001), but not with the transformation to acute leukemia.0.0035287442012JAK2;INSL695073770GA,T
rs854560229768395444PON1umls:C0085669BeFreeNQO1 rs1800566 (C609T), PON1 rs662 (Q192R), and PON1 rs854560 (L55M) polymorphisms segregate the risk of childhood acute leukemias according to age range distribution.0.0002714422012PON1795316772AC,G,N,T
GWASdb Annotation(Total Genotypes:0)
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GWASdb Snp Trait(Total Genotypes:0)
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Mapped by lexical matching(Total Items:0)
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Mapped by homologous gene(Total Items:0)
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