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Pediatric Disease Annotations & Medicines



   central nervous system lymphoma
  

Disease ID 1429
Disease central nervous system lymphoma
Definition
A non-Hodgkin or Hodgkin lymphoma that arises in the brain or spinal cord as a primary lesion. There is no evidence of lymphoma outside the central nervous system at the time of diagnosis.
Synonym
central lymphoma nervous system
cns lymphoma
cns lymphomas
lymphoma cns
malignant lymphomas of cns
malignant lymphomas of the cns
DOID
UMLS
C0742472
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:26)
C0024299  |  lymphoma  |  3
C0281658  |  primary intraocular lymphoma  |  2
C0281658  |  intraocular lymphoma  |  2
C0730306  |  ocular lymphoma  |  2
C0001175  |  acquired immune deficiency  |  1
C0023418  |  leukemia  |  1
C0006413  |  burkitt lymphoma  |  1
C0011848  |  diabetes insipidus  |  1
C0003864  |  arthritis  |  1
C0497327  |  dementia  |  1
C0002878  |  hemolytic anemia  |  1
C0011847  |  diabetes  |  1
C0024141  |  systemic lupus erythematosus  |  1
C0017636  |  glioblastoma  |  1
C0024299  |  lymphomas  |  1
C0023492  |  t-cell leukemia  |  1
C0023493  |  adult t-cell leukemia  |  1
C0002871  |  anemia  |  1
C0085113  |  neurofibromatosis  |  1
C0002880  |  autoimmune hemolytic anemia  |  1
C0007688  |  central retinal artery occlusion  |  1
C0003873  |  rheumatoid arthritis  |  1
C0035302  |  retinal artery occlusion  |  1
C0001175  |  acquired immune deficiency syndrome  |  1
C1621958  |  glioblastoma multiforme  |  1
C0409974  |  lupus erythematosus  |  1
Curated Gene(Waiting for update.)
Inferring Gene(Waiting for update.)
Text Mined Gene
Entrez_id | Symbol | Score | Resource(Total Genes:133)
84245  |  MRI1  |  DISEASES
608  |  TNFRSF17  |  DISEASES
6948  |  TCN2  |  DISEASES
7494  |  XBP1  |  DISEASES
2091  |  FBL  |  DISEASES
3558  |  IL2  |  DISEASES
9896  |  FIG4  |  DISEASES
55754  |  TMEM30A  |  DISEASES
51185  |  CRBN  |  DISEASES
604  |  BCL6  |  DISEASES
5947  |  RBP1  |  DISEASES
7128  |  TNFAIP3  |  DISEASES
9429  |  ABCG2  |  DISEASES
114784  |  CSMD2  |  DISEASES
1236  |  CCR7  |  DISEASES
968  |  CD68  |  DISEASES
4005  |  LMO2  |  DISEASES
3569  |  IL6  |  DISEASES
8140  |  SLC7A5  |  DISEASES
23495  |  TNFRSF13B  |  DISEASES
7597  |  ZBTB25  |  DISEASES
4481  |  MSR1  |  DISEASES
6009  |  RHEB  |  DISEASES
7305  |  TYROBP  |  DISEASES
5605  |  MAP2K2  |  DISEASES
5264  |  PHYH  |  DISEASES
55850  |  USE1  |  DISEASES
943  |  TNFRSF8  |  DISEASES
60482  |  SLC5A7  |  DISEASES
6774  |  STAT3  |  DISEASES
939  |  CD27  |  DISEASES
7157  |  TP53  |  DISEASES
9180  |  OSMR  |  DISEASES
4594  |  MUT  |  DISEASES
4794  |  NFKBIE  |  DISEASES
80005  |  DOCK5  |  DISEASES
26011  |  TENM4  |  DISEASES
2838  |  GPR15  |  DISEASES
10563  |  CXCL13  |  DISEASES
56896  |  DPYSL5  |  DISEASES
909  |  CD1A  |  DISEASES
7832  |  BTG2  |  DISEASES
115650  |  TNFRSF13C  |  DISEASES
643  |  CXCR5  |  DISEASES
51705  |  EMCN  |  DISEASES
9607  |  CARTPT  |  DISEASES
84624  |  FNDC1  |  DISEASES
114788  |  CSMD3  |  DISEASES
23588  |  KLHDC2  |  DISEASES
322  |  APBB1  |  DISEASES
6778  |  STAT6  |  DISEASES
4255  |  MGMT  |  DISEASES
10886  |  NPFFR2  |  DISEASES
695  |  BTK  |  DISEASES
2629  |  GBA  |  DISEASES
57381  |  RHOJ  |  DISEASES
10318  |  TNIP1  |  DISEASES
260436  |  FDCSP  |  DISEASES
4684  |  NCAM1  |  DISEASES
27086  |  FOXP1  |  DISEASES
10892  |  MALT1  |  DISEASES
10938  |  EHD1  |  DISEASES
1879  |  EBF1  |  DISEASES
1303  |  COL12A1  |  DISEASES
81857  |  MED25  |  DISEASES
8204  |  NRIP1  |  DISEASES
284359  |  IZUMO1  |  DISEASES
5580  |  PRKCD  |  DISEASES
23583  |  SMUG1  |  DISEASES
3266  |  ERAS  |  DISEASES
51393  |  TRPV2  |  DISEASES
1809  |  DPYSL3  |  DISEASES
6890  |  TAP1  |  DISEASES
6050  |  RNH1  |  DISEASES
5789  |  PTPRD  |  DISEASES
1612  |  DAPK1  |  DISEASES
5079  |  PAX5  |  DISEASES
56241  |  SUSD2  |  DISEASES
112476  |  PRRT2  |  DISEASES
9332  |  CD163  |  DISEASES
57565  |  KLHL14  |  DISEASES
4311  |  MME  |  DISEASES
10848  |  PPP1R13L  |  DISEASES
9760  |  TOX  |  DISEASES
80178  |  C16orf59  |  DISEASES
4548  |  MTR  |  DISEASES
359948  |  IRF2BP2  |  DISEASES
1378  |  CR1  |  DISEASES
23345  |  SYNE1  |  DISEASES
5788  |  PTPRC  |  DISEASES
3068  |  HDGF  |  DISEASES
5796  |  PTPRK  |  DISEASES
4580  |  MTX1  |  DISEASES
3713  |  IVL  |  DISEASES
5654  |  HTRA1  |  DISEASES
639  |  PRDM1  |  DISEASES
965  |  CD58  |  DISEASES
1847  |  DUSP5  |  DISEASES
541466  |  CT45A1  |  DISEASES
80351  |  TNKS2  |  DISEASES
10673  |  TNFSF13B  |  DISEASES
4524  |  MTHFR  |  DISEASES
10257  |  ABCC4  |  DISEASES
10590  |  SCGN  |  DISEASES
4609  |  MYC  |  DISEASES
551  |  AVP  |  DISEASES
1646  |  AKR1C2  |  DISEASES
3662  |  IRF4  |  DISEASES
399  |  RHOH  |  DISEASES
238  |  ALK  |  DISEASES
974  |  CD79B  |  DISEASES
6696  |  SPP1  |  DISEASES
220963  |  SLC16A9  |  DISEASES
6387  |  CXCL12  |  DISEASES
114884  |  OSBPL10  |  DISEASES
84433  |  CARD11  |  DISEASES
7852  |  CXCR4  |  DISEASES
5349  |  FXYD3  |  DISEASES
23210  |  JMJD6  |  DISEASES
1029  |  CDKN2A  |  DISEASES
10672  |  GNA13  |  DISEASES
7072  |  TIA1  |  DISEASES
4615  |  MYD88  |  DISEASES
79718  |  TBL1XR1  |  DISEASES
81704  |  DOCK8  |  DISEASES
9734  |  HDAC9  |  DISEASES
3586  |  IL10  |  DISEASES
6513  |  SLC2A1  |  DISEASES
257144  |  GCSAM  |  DISEASES
345778  |  MTX3  |  DISEASES
10687  |  PNMA2  |  DISEASES
567  |  B2M  |  DISEASES
407975  |  MIR17HG  |  DISEASES
Locus(Waiting for update.)
Disease ID 1429
Disease central nervous system lymphoma
Integrated Phenotype(Waiting for update.)
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:17)
HP:0002665  |  Lymphoma  |  3
HP:0002664  |  Neoplasia  |  2
HP:0002721  |  Immunodeficiency  |  2
HP:0001370  |  Rheumatoid arthritis  |  1
HP:0000726  |  Dementia  |  1
HP:0001369  |  Arthritis  |  1
HP:0001909  |  Leukemia  |  1
HP:0002902  |  Hyponatremia  |  1
HP:0002725  |  Systemic lupus erythematosus  |  1
HP:0001890  |  Autoimmune hemolytic anemia  |  1
HP:0001903  |  Anemia  |  1
HP:0012174  |  Glioblastoma multiforme  |  1
HP:0030080  |  Burkitt lymphoma  |  1
HP:0000873  |  Diabetes insipidus  |  1
HP:0001067  |  Neurofibromas  |  1
HP:0001878  |  Haemolytic anaemia  |  1
HP:0100843  |  Glioblastoma  |  1
Disease ID 1429
Disease central nervous system lymphoma
Manually Symptom
UMLS  | Name(Total Manually Symptoms:4)
C0040053  |  thrombosis
C0040038  |  thromboembolism
C0027831  |  neurofibromatosis type 1
C0020524  |  disorder of excessive somnolence
Text Mined Symptom
UMLS | Name | Sentences' Count(Total Symptoms:1)
Manually Genotype(Total Text Mining Genotypes:0)
(Waiting for update.)
All Snps(Total Genotypes:0)
(Waiting for update.)
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.)