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Pediatric Disease Annotations & Medicines



   lymphoblastic lymphoma
  

Disease ID 1202
Disease lymphoblastic lymphoma
Definition
A lymphoma composed of immature small to medium-sized precursor lymphoid cells (lymphoblasts). It includes the B- and T-cell lymphoblastic lymphoma.
Synonym
[m]lymphoblastic lymphoma nos
diffuse lymphoblastic lymphoma
diffuse lymphoblastic lymphosarcoma
diffuse lymphoblastic malignant lymphoma
diffuse lymphoblastoma
diffuse non-hodgkin lymphoma, lymphoblastic
diffuse non-hodgkin's lymphoma, lymphoblastic
diffuse non-hodgkin's lymphoma, lymphoblastic (clinical)
diffuse non-hodgkin's lymphoma, lymphoblastic (disorder)
lymphoblastic lymphoma, diffuse
lymphoblastic lymphosarcoma
lymphoblastic malignant lymphoma
lymphoblastoma
lymphoblastoma [obs]
lymphoma lymphoblastic
lymphoma, lymphoblastic, malignant
malignant lymphoma - lymphoblastic
malignant lymphoma, convoluted cell
malignant lymphoma, convoluted cell [obs]
malignant lymphoma, lymphoblastic
malignant lymphoma, lymphoblastic (morphologic abnormality)
malignant lymphoma, lymphoblastic -retired-
precursor cell lymphoblastic lymphoma
precursor cell lymphoblastic lymphoma (morphologic abnormality)
precursor lymphoblastic lymphoma
DOID
UMLS
C0079748
SNOMED-CT
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:18)
C0024299  |  lymphoma  |  4
C0023470  |  myeloid leukemia  |  3
C0019618  |  histiocytosis  |  2
C0023467  |  acute myeloid leukemia  |  2
C0023418  |  leukemia  |  2
C0042769  |  virus infection  |  2
C0019621  |  langerhans cell histiocytosis  |  2
C0023473  |  chronic myeloid leukemia  |  1
C0023448  |  lymphoblastic leukemia  |  1
C0023449  |  acute lymphoblastic leukemia  |  1
C0151332  |  active tuberculosis  |  1
C0028754  |  obesity  |  1
C0041296  |  tuberculosis  |  1
C1258215  |  ileus  |  1
C0001125  |  lactic acidosis  |  1
C0079731  |  b-cell lymphoma  |  1
C0494165  |  hepatic metastasis  |  1
C1333375  |  ectopic thymus  |  1
Curated Gene(Waiting for update.)
Inferring Gene(Waiting for update.)
Text Mined Gene
Entrez_id | Symbol | Score | Resource(Total Genes:170)
972  |  CD74  |  DISEASES
9603  |  NFE2L3  |  DISEASES
933  |  CD22  |  DISEASES
6561  |  SLC13A1  |  DISEASES
990  |  CDC6  |  DISEASES
1113  |  CHGA  |  DISEASES
973  |  CD79A  |  DISEASES
51384  |  WNT16  |  DISEASES
944  |  TNFSF8  |  DISEASES
4353  |  MPO  |  DISEASES
1440  |  CSF3  |  DISEASES
8456  |  FOXN1  |  DISEASES
952  |  CD38  |  DISEASES
3558  |  IL2  |  DISEASES
116449  |  CLNK  |  DISEASES
595  |  CCND1  |  DISEASES
1027  |  CDKN1B  |  DISEASES
2026  |  ENO2  |  DISEASES
26127  |  FGFR1OP2  |  DISEASES
10279  |  PRSS16  |  DISEASES
6534  |  SLC6A7  |  DISEASES
604  |  BCL6  |  DISEASES
22924  |  MAPRE3  |  DISEASES
5624  |  PROC  |  DISEASES
27434  |  POLM  |  DISEASES
6299  |  SALL1  |  DISEASES
3998  |  LMAN1  |  DISEASES
57418  |  WDR18  |  DISEASES
10752  |  CHL1  |  DISEASES
8739  |  HRK  |  DISEASES
1840  |  DTX1  |  DISEASES
9883  |  POM121  |  DISEASES
4005  |  LMO2  |  DISEASES
10017  |  BCL2L10  |  DISEASES
10113  |  PREB  |  DISEASES
4069  |  LYZ  |  DISEASES
8140  |  SLC7A5  |  DISEASES
1975  |  EIF4B  |  DISEASES
945  |  CD33  |  DISEASES
4025  |  LPO  |  DISEASES
84662  |  GLIS2  |  DISEASES
9618  |  TRAF4  |  DISEASES
6929  |  TCF3  |  DISEASES
5264  |  PHYH  |  DISEASES
6855  |  SYP  |  DISEASES
943  |  TNFRSF8  |  DISEASES
10382  |  TUBB4A  |  DISEASES
4066  |  LYL1  |  DISEASES
5924  |  RASGRF2  |  DISEASES
4683  |  NBN  |  DISEASES
7994  |  KAT6A  |  DISEASES
1021  |  CDK6  |  DISEASES
51411  |  BIN2  |  DISEASES
23067  |  SETD1B  |  DISEASES
7157  |  TP53  |  DISEASES
6455  |  SH3GL1  |  DISEASES
63978  |  PRDM14  |  DISEASES
1030  |  CDKN2B  |  DISEASES
4851  |  NOTCH1  |  DISEASES
55294  |  FBXW7  |  DISEASES
2838  |  GPR15  |  DISEASES
7345  |  UCHL1  |  DISEASES
3815  |  KIT  |  DISEASES
89858  |  SIGLEC12  |  DISEASES
6777  |  STAT5B  |  DISEASES
1973  |  EIF4A1  |  DISEASES
6886  |  TAL1  |  DISEASES
10206  |  TRIM13  |  DISEASES
10818  |  FRS2  |  DISEASES
201161  |  CENPV  |  DISEASES
290  |  ANPEP  |  DISEASES
915  |  CD3D  |  DISEASES
81620  |  CDT1  |  DISEASES
8772  |  FADD  |  DISEASES
613  |  BCR  |  DISEASES
171558  |  PTCRA  |  DISEASES
8625  |  RFXANK  |  DISEASES
8028  |  MLLT10  |  DISEASES
27087  |  B3GAT1  |  DISEASES
64978  |  MRPL38  |  DISEASES
3265  |  HRAS  |  DISEASES
947  |  CD34  |  DISEASES
10125  |  RASGRP1  |  DISEASES
924  |  CD7  |  DISEASES
7172  |  TPMT  |  DISEASES
84883  |  AIFM2  |  DISEASES
92745  |  SLC38A5  |  DISEASES
931  |  MS4A1  |  DISEASES
147912  |  SIX5  |  DISEASES
4684  |  NCAM1  |  DISEASES
55024  |  BANK1  |  DISEASES
1351  |  COX8A  |  DISEASES
6664  |  SOX11  |  DISEASES
923  |  CD6  |  DISEASES
11284  |  PNKP  |  DISEASES
2027  |  ENO3  |  DISEASES
951  |  CD37  |  DISEASES
1974  |  EIF4A2  |  DISEASES
3563  |  IL3RA  |  DISEASES
3543  |  IGLL1  |  DISEASES
81608  |  FIP1L1  |  DISEASES
3932  |  LCK  |  DISEASES
3824  |  KLRD1  |  DISEASES
4004  |  LMO1  |  DISEASES
23583  |  SMUG1  |  DISEASES
3266  |  ERAS  |  DISEASES
6776  |  STAT5A  |  DISEASES
132884  |  EVC2  |  DISEASES
921  |  CD5  |  DISEASES
2335  |  FN1  |  DISEASES
219844  |  HYLS1  |  DISEASES
1822  |  ATN1  |  DISEASES
5079  |  PAX5  |  DISEASES
4149  |  MAX  |  DISEASES
2526  |  FUT4  |  DISEASES
117583  |  PARD3B  |  DISEASES
7037  |  TFRC  |  DISEASES
6693  |  SPN  |  DISEASES
4311  |  MME  |  DISEASES
5475  |  PPEF1  |  DISEASES
5693  |  PSMB5  |  DISEASES
961  |  CD47  |  DISEASES
1378  |  CR1  |  DISEASES
1380  |  CR2  |  DISEASES
5788  |  PTPRC  |  DISEASES
51022  |  GLRX2  |  DISEASES
1314  |  COPA  |  DISEASES
154215  |  NKAIN2  |  DISEASES
4942  |  OAT  |  DISEASES
914  |  CD2  |  DISEASES
965  |  CD58  |  DISEASES
3195  |  TLX1  |  DISEASES
959  |  CD40LG  |  DISEASES
1647  |  GADD45A  |  DISEASES
1791  |  DNTT  |  DISEASES
25  |  ABL1  |  DISEASES
100  |  ADA  |  DISEASES
896  |  CCND3  |  DISEASES
5090  |  PBX3  |  DISEASES
7027  |  TFDP1  |  DISEASES
4524  |  MTHFR  |  DISEASES
4609  |  MYC  |  DISEASES
64225  |  ATL2  |  DISEASES
3559  |  IL2RA  |  DISEASES
54790  |  TET2  |  DISEASES
4267  |  CD99  |  DISEASES
80333  |  KCNIP4  |  DISEASES
7750  |  ZMYM2  |  DISEASES
238  |  ALK  |  DISEASES
340152  |  ZC3H12D  |  DISEASES
3239  |  HOXD13  |  DISEASES
838  |  CASP5  |  DISEASES
347734  |  SLC35B2  |  DISEASES
196410  |  METTL7B  |  DISEASES
83478  |  ARHGAP24  |  DISEASES
55120  |  FANCL  |  DISEASES
7441  |  VPREB1  |  DISEASES
29072  |  SETD2  |  DISEASES
2260  |  FGFR1  |  DISEASES
81542  |  TMX1  |  DISEASES
1438  |  CSF2RA  |  DISEASES
1029  |  CDKN2A  |  DISEASES
2313  |  FLI1  |  DISEASES
2130  |  EWSR1  |  DISEASES
7072  |  TIA1  |  DISEASES
6158  |  RPL28  |  DISEASES
26054  |  SENP6  |  DISEASES
4049  |  LTA  |  DISEASES
22862  |  FNDC3A  |  DISEASES
930  |  CD19  |  DISEASES
Locus(Waiting for update.)
Disease ID 1202
Disease lymphoblastic lymphoma
Integrated Phenotype(Waiting for update.)
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:16)
HP:0002665  |  Lymphoma  |  4
HP:0012324  |  Myeloid leukemia  |  3
HP:0004808  |  Acute myelogenous leukemia  |  2
HP:0100727  |  Histiocytosis  |  2
HP:0001909  |  Leukemia  |  2
HP:0006721  |  Acute lymphocytic leukemia  |  1
HP:0002664  |  Neoplasia  |  1
HP:0012191  |  B-cell lymphoma  |  1
HP:0005506  |  Chronic myeloid leukemia  |  1
HP:0003128  |  Lactic acidosis  |  1
HP:0001513  |  Obesity  |  1
HP:0001941  |  acidemia  |  1
HP:0002595  |  Gastrointestinal atony  |  1
HP:0001880  |  Eosinophilia  |  1
HP:0002716  |  Lymph node hyperplasia  |  1
HP:0002202  |  Pleural effusion  |  1
Disease ID 1202
Disease lymphoblastic lymphoma
Manually Symptom
UMLS  | Name(Total Manually Symptoms:4)
C0400979  |  biliary obstruction
C0347016  |  spinal cord metastasis
C0032227  |  pleural effusions
C0018133  |  graft-versus-host disease
Text Mined Symptom(Waiting for update.)
Manually Genotype(Total Text Mining 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
rs1051266184585674524MTHFRumls:C0079748BeFreeWe investigated preliminarily whether methylenetetrahydrofolate reductase (MTHFR) 677C/T or reduced folate carrier 1 (RFC1) 80G/A polymorphisms were associated with toxicities during maintenance chemotherapy with mercaptopurine (6MP) and methotrexate (MTX) in children with acute lymphoblastic leukemia or lymphoblastic lymphoma.0.0005428842008SLC19A12145537880TC
rs368087026184585674524MTHFRumls:C0079748BeFreeWe investigated preliminarily whether methylenetetrahydrofolate reductase (MTHFR) 677C/T or reduced folate carrier 1 (RFC1) 80G/A polymorphisms were associated with toxicities during maintenance chemotherapy with mercaptopurine (6MP) and methotrexate (MTX) in children with acute lymphoblastic leukemia or lymphoblastic lymphoma.0.0005428842008SLC19A12145530890GA
rs386514057184585674524MTHFRumls:C0079748BeFreeWe investigated preliminarily whether methylenetetrahydrofolate reductase (MTHFR) 677C/T or reduced folate carrier 1 (RFC1) 80G/A polymorphisms were associated with toxicities during maintenance chemotherapy with mercaptopurine (6MP) and methotrexate (MTX) in children with acute lymphoblastic leukemia or lymphoblastic lymphoma.0.0005428842008NANANANANA
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.)