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PedAM

Pediatric Disease Annotations & Medicines



   prolymphocytic leukemia
  

Disease ID 1795
Disease prolymphocytic leukemia
Definition
A chronic leukemia characterized by a large number of circulating prolymphocytes. It can arise spontaneously or as a consequence of transformation of CHRONIC LYMPHOCYTIC LEUKEMIA.
Synonym
[m]prolymphocytic leukaemia
[m]prolymphocytic leukemia
leukemia, prolymphocytic
leukemia, prolymphocytic [disease/finding]
leukemias, prolymphocytic
pll
pll - prolymphocytic leukaemia
pll - prolymphocytic leukemia
pll prolymphocytic leukemia
pro-lymphocytic leukemia
prolymphocytic leukaemia
prolymphocytic leukaemia (clinical)
prolymphocytic leukaemia -retired-
prolymphocytic leukemia (b or t)
prolymphocytic leukemia (b or t-cell)
prolymphocytic leukemia (clinical)
prolymphocytic leukemia (disorder)
prolymphocytic leukemia (morphologic abnormality)
prolymphocytic leukemia -retired-
prolymphocytic leukemia, no icd-o subtype (morphologic abnormality)
prolymphocytic leukemias
DOID
UMLS
C0023486
MeSH
SNOMED-CT
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:9)
C0023434  |  chronic lymphocytic leukemia  |  2
C0024299  |  lymphoma  |  2
C0023448  |  lymphocytic leukemia  |  1
C0023418  |  leukemia  |  1
C0017601  |  glaucoma  |  1
C0002880  |  autoimmune hemolytic anemia  |  1
C0042384  |  vasculitis  |  1
C0019829  |  hodgkin's lymphoma  |  1
C0002878  |  hemolytic anemia  |  1
Curated Gene(Waiting for update.)
Inferring Gene(Waiting for update.)
Text Mined Gene
Entrez_id | Symbol | Score | Resource(Total Genes:105)
9052  |  GPRC5A  |  DISEASES
340533  |  KIAA2022  |  DISEASES
933  |  CD22  |  DISEASES
602  |  BCL3  |  DISEASES
54  |  ACP5  |  DISEASES
10226  |  PLIN3  |  DISEASES
944  |  TNFSF8  |  DISEASES
952  |  CD38  |  DISEASES
3558  |  IL2  |  DISEASES
595  |  CCND1  |  DISEASES
604  |  BCL6  |  DISEASES
5341  |  PLEK  |  DISEASES
4695  |  NDUFA2  |  DISEASES
8572  |  PDLIM4  |  DISEASES
10752  |  CHL1  |  DISEASES
301  |  ANXA1  |  DISEASES
23213  |  SULF1  |  DISEASES
10113  |  PREB  |  DISEASES
3682  |  ITGAE  |  DISEASES
943  |  TNFRSF8  |  DISEASES
7294  |  TXK  |  DISEASES
3383  |  ICAM1  |  DISEASES
7535  |  ZAP70  |  DISEASES
7994  |  KAT6A  |  DISEASES
3687  |  ITGAX  |  DISEASES
7157  |  TP53  |  DISEASES
207  |  AKT1  |  DISEASES
4863  |  NPAT  |  DISEASES
472  |  ATM  |  DISEASES
116337  |  PANX3  |  DISEASES
7345  |  UCHL1  |  DISEASES
89858  |  SIGLEC12  |  DISEASES
2215  |  FCGR3B  |  DISEASES
327  |  APEH  |  DISEASES
1437  |  CSF2  |  DISEASES
9317  |  PTER  |  DISEASES
290  |  ANPEP  |  DISEASES
133418  |  EMB  |  DISEASES
27087  |  B3GAT1  |  DISEASES
924  |  CD7  |  DISEASES
931  |  MS4A1  |  DISEASES
4261  |  CIITA  |  DISEASES
4684  |  NCAM1  |  DISEASES
6470  |  SHMT1  |  DISEASES
6664  |  SOX11  |  DISEASES
55  |  ACPP  |  DISEASES
951  |  CD37  |  DISEASES
8519  |  IFITM1  |  DISEASES
942  |  CD86  |  DISEASES
3932  |  LCK  |  DISEASES
966  |  CD59  |  DISEASES
921  |  CD5  |  DISEASES
3716  |  JAK1  |  DISEASES
9623  |  TCL1B  |  DISEASES
1399  |  CRKL  |  DISEASES
2331  |  FMOD  |  DISEASES
9260  |  PDLIM7  |  DISEASES
219844  |  HYLS1  |  DISEASES
64919  |  BCL11B  |  DISEASES
9961  |  MVP  |  DISEASES
5893  |  RAD52  |  DISEASES
55959  |  SULF2  |  DISEASES
2114  |  ETS2  |  DISEASES
3164  |  NR4A1  |  DISEASES
4311  |  MME  |  DISEASES
4515  |  MTCP1  |  DISEASES
1380  |  CR2  |  DISEASES
5788  |  PTPRC  |  DISEASES
2214  |  FCGR3A  |  DISEASES
4288  |  MKI67  |  DISEASES
79184  |  BRCC3  |  DISEASES
914  |  CD2  |  DISEASES
1847  |  DUSP5  |  DISEASES
959  |  CD40LG  |  DISEASES
1791  |  DNTT  |  DISEASES
100  |  ADA  |  DISEASES
1043  |  CD52  |  DISEASES
4609  |  MYC  |  DISEASES
54880  |  BCOR  |  DISEASES
3559  |  IL2RA  |  DISEASES
11200  |  CHEK2  |  DISEASES
238  |  ALK  |  DISEASES
2113  |  ETS1  |  DISEASES
7187  |  TRAF3  |  DISEASES
974  |  CD79B  |  DISEASES
5450  |  POU2AF1  |  DISEASES
3122  |  HLA-DRA  |  DISEASES
10517  |  FBXW10  |  DISEASES
2120  |  ETV6  |  DISEASES
23308  |  ICOSLG  |  DISEASES
8115  |  TCL1A  |  DISEASES
2011  |  MARK2  |  DISEASES
3718  |  JAK3  |  DISEASES
59339  |  PLEKHA2  |  DISEASES
1029  |  CDKN2A  |  DISEASES
83876  |  MRO  |  DISEASES
3702  |  ITK  |  DISEASES
30816  |  ERVW-1  |  DISEASES
4345  |  CD200  |  DISEASES
4603  |  MYBL1  |  DISEASES
930  |  CD19  |  DISEASES
3684  |  ITGAM  |  DISEASES
567  |  B2M  |  DISEASES
2323  |  FLT3LG  |  DISEASES
27004  |  TCL6  |  DISEASES
Locus(Waiting for update.)
Disease ID 1795
Disease prolymphocytic leukemia
Integrated Phenotype(Waiting for update.)
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:9)
HP:0005550  |  Chronic lymphatic leukemia  |  2
HP:0002665  |  Lymphoma  |  2
HP:0000501  |  Glaucoma  |  1
HP:0001890  |  Autoimmune hemolytic anemia  |  1
HP:0001909  |  Leukemia  |  1
HP:0002664  |  Neoplasia  |  1
HP:0001878  |  Haemolytic anaemia  |  1
HP:0012189  |  Hodgkin disease  |  1
HP:0002633  |  Vasculitis  |  1
Disease ID 1795
Disease prolymphocytic leukemia
Manually Symptom(Waiting for update.)
Text Mined Symptom(Waiting for update.)
Manually Genotype(Total Text Mining Genotypes:0)
(Waiting for update.)
All Snps(Total Genotypes:1)
snpId pubmedId geneId geneSymbol diseaseId sourceId sentence score Year geneSymbol_dbSNP CHROMOSOME POS REF ALT
rs11348802222230299673BRAFumls:C0023486BeFreeIncidence of the BRAF V600E mutation in chronic lymphocytic leukaemia and prolymphocytic leukaemia.0.0002714422012BRAF7140753336AT,G,C
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.)