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Pediatric Disease Annotations & Medicines



   childhood leukemia
  

Disease ID 1751
Disease childhood leukemia
Definition

Leukemia is cancer of the white blood cells. It is the most common type of childhood cancer. Your blood cells form in your bone marrow. White blood cells help your body fight infection. In leukemia, the bone marrow produces abnormal white blood cells. These cells crowd out the healthy blood cells, making it hard for blood to do its work.

Leukemia can develop quickly or slowly. Acute leukemia is a fast growing type while chronic leukemia grows slowly. Children with leukemia usually have one of the acute types.

Symptoms include

  • Infections
  • Fever
  • Loss of appetite
  • Tiredness
  • Easy bruising or bleeding
  • Swollen lymph nodes
  • Night sweats
  • Shortness of breath
  • Pain in the bones or joints

Risk factors for childhood leukemia include having a brother or sister with leukemia, having certain genetic disorders and having had radiation or chemotherapy. Treatment often cures childhood leukemia. Treatment options include chemotherapy, other drug therapy and radiation. In some cases bone marrow and blood stem cell transplantation might help.

NIH: National Cancer Institute


Synonym
leukemia, childhood
DOID
UMLS
C1332977
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:7)
C0178664  |  glomerulosclerosis  |  1
C0023418  |  leukemia  |  1
C0000786  |  miscarriage  |  1
C0023448  |  lymphoblastic leukemia  |  1
C0017668  |  focal glomerulosclerosis  |  1
C0948265  |  metabolic syndrome  |  1
C0002871  |  anemia  |  1
Curated Gene(Waiting for update.)
Inferring Gene
Entrez_id | Symbol | Resource(Total Genes:1)
3077  |  HFE  |  infer
Text Mined Gene
Entrez_id | Symbol | Score | Resource(Total Genes:172)
928  |  CD9  |  DISEASES
29850  |  TRPM5  |  DISEASES
7022  |  TFAP2C  |  DISEASES
1053  |  CEBPE  |  DISEASES
201294  |  UNC13D  |  DISEASES
6948  |  TCN2  |  DISEASES
4150  |  MAZ  |  DISEASES
23581  |  CASP14  |  DISEASES
3202  |  HOXA5  |  DISEASES
3203  |  HOXA6  |  DISEASES
1440  |  CSF3  |  DISEASES
952  |  CD38  |  DISEASES
3111  |  HLA-DOA  |  DISEASES
6534  |  SLC6A7  |  DISEASES
2908  |  NR3C1  |  DISEASES
1894  |  ECT2  |  DISEASES
3485  |  IGFBP2  |  DISEASES
2322  |  FLT3  |  DISEASES
6431  |  SRSF6  |  DISEASES
5184  |  PEPD  |  DISEASES
9271  |  PIWIL1  |  DISEASES
2952  |  GSTT1  |  DISEASES
54567  |  DLL4  |  DISEASES
6320  |  CLEC11A  |  DISEASES
4298  |  MLLT1  |  DISEASES
1571  |  CYP2E1  |  DISEASES
3110  |  MNX1  |  DISEASES
5914  |  RARA  |  DISEASES
10752  |  CHL1  |  DISEASES
55270  |  NUDT15  |  DISEASES
64005  |  MYO1G  |  DISEASES
8737  |  RIPK1  |  DISEASES
10113  |  PREB  |  DISEASES
8099  |  CDK2AP1  |  DISEASES
1031  |  CDKN2C  |  DISEASES
8178  |  ELL  |  DISEASES
25939  |  SAMHD1  |  DISEASES
3783  |  KCNN4  |  DISEASES
6929  |  TCF3  |  DISEASES
645  |  BLVRB  |  DISEASES
3589  |  IL11  |  DISEASES
4552  |  MTRR  |  DISEASES
80321  |  CEP70  |  DISEASES
7994  |  KAT6A  |  DISEASES
6821  |  SUOX  |  DISEASES
7157  |  TP53  |  DISEASES
57332  |  CBX8  |  DISEASES
6455  |  SH3GL1  |  DISEASES
55840  |  EAF2  |  DISEASES
4594  |  MUT  |  DISEASES
4103  |  MAGEA4  |  DISEASES
84159  |  ARID5B  |  DISEASES
23389  |  MED13L  |  DISEASES
5018  |  OXA1L  |  DISEASES
23522  |  KAT6B  |  DISEASES
115653  |  KIR3DL3  |  DISEASES
84464  |  SLX4  |  DISEASES
2672  |  GFI1  |  DISEASES
5966  |  REL  |  DISEASES
64399  |  HHIP  |  DISEASES
56979  |  PRDM9  |  DISEASES
1437  |  CSF2  |  DISEASES
30012  |  TLX3  |  DISEASES
89927  |  C16orf45  |  DISEASES
861  |  RUNX1  |  DISEASES
8772  |  FADD  |  DISEASES
3479  |  IGF1  |  DISEASES
8988  |  HSPB3  |  DISEASES
613  |  BCR  |  DISEASES
29  |  ABR  |  DISEASES
2237  |  FEN1  |  DISEASES
8028  |  MLLT10  |  DISEASES
3213  |  HOXB3  |  DISEASES
6573  |  SLC19A1  |  DISEASES
3265  |  HRAS  |  DISEASES
947  |  CD34  |  DISEASES
2944  |  GSTM1  |  DISEASES
84883  |  AIFM2  |  DISEASES
5306  |  PITPNA  |  DISEASES
6950  |  TCP1  |  DISEASES
6470  |  SHMT1  |  DISEASES
348654  |  GEN1  |  DISEASES
1728  |  NQO1  |  DISEASES
2193  |  FARSA  |  DISEASES
1827  |  RCAN1  |  DISEASES
6181  |  RPLP2  |  DISEASES
6478  |  SIAH2  |  DISEASES
55  |  ACPP  |  DISEASES
57491  |  AHRR  |  DISEASES
951  |  CD37  |  DISEASES
8738  |  CRADD  |  DISEASES
7490  |  WT1  |  DISEASES
71  |  ACTG1  |  DISEASES
10320  |  IKZF1  |  DISEASES
10732  |  TCFL5  |  DISEASES
10608  |  MXD4  |  DISEASES
63826  |  SRR  |  DISEASES
4602  |  MYB  |  DISEASES
8805  |  TRIM24  |  DISEASES
5781  |  PTPN11  |  DISEASES
3010  |  HIST1H1T  |  DISEASES
7518  |  XRCC4  |  DISEASES
3205  |  HOXA9  |  DISEASES
1809  |  DPYSL3  |  DISEASES
79971  |  WLS  |  DISEASES
84870  |  RSPO3  |  DISEASES
60  |  ACTB  |  DISEASES
9961  |  MVP  |  DISEASES
728378  |  POTEF  |  DISEASES
2764  |  GMFB  |  DISEASES
131873  |  COL6A6  |  DISEASES
3201  |  HOXA4  |  DISEASES
7037  |  TFRC  |  DISEASES
4311  |  MME  |  DISEASES
5167  |  ENPP1  |  DISEASES
4548  |  MTR  |  DISEASES
8676  |  STX11  |  DISEASES
4121  |  MAN1A1  |  DISEASES
253738  |  EBF3  |  DISEASES
262  |  AMD1  |  DISEASES
10962  |  MLLT11  |  DISEASES
474384  |  F8A3  |  DISEASES
8036  |  SHOC2  |  DISEASES
474383  |  F8A2  |  DISEASES
4893  |  NRAS  |  DISEASES
9446  |  GSTO1  |  DISEASES
10660  |  LBX1  |  DISEASES
2334  |  AFF2  |  DISEASES
1791  |  DNTT  |  DISEASES
1289  |  COL5A1  |  DISEASES
25  |  ABL1  |  DISEASES
714  |  C1QC  |  DISEASES
316  |  AOX1  |  DISEASES
1302  |  COL11A2  |  DISEASES
8242  |  KDM5C  |  DISEASES
4879  |  NPPB  |  DISEASES
5305  |  PIP4K2A  |  DISEASES
4524  |  MTHFR  |  DISEASES
2623  |  GATA1  |  DISEASES
3105  |  HLA-A  |  DISEASES
5987  |  TRIM27  |  DISEASES
5101  |  PCDH9  |  DISEASES
4609  |  MYC  |  DISEASES
7102  |  TSPAN7  |  DISEASES
7163  |  TPD52  |  DISEASES
7020  |  TFAP2A  |  DISEASES
7223  |  TRPC4  |  DISEASES
1543  |  CYP1A1  |  DISEASES
4300  |  MLLT3  |  DISEASES
8644  |  AKR1C3  |  DISEASES
3486  |  IGFBP3  |  DISEASES
286530  |  P2RY8  |  DISEASES
64109  |  CRLF2  |  DISEASES
192668  |  CYS1  |  DISEASES
7862  |  BRPF1  |  DISEASES
64115  |  C10orf54  |  DISEASES
4299  |  AFF1  |  DISEASES
3122  |  HLA-DRA  |  DISEASES
4629  |  MYH11  |  DISEASES
2120  |  ETV6  |  DISEASES
1747  |  DLX3  |  DISEASES
960  |  CD44  |  DISEASES
3109  |  HLA-DMB  |  DISEASES
10499  |  NCOA2  |  DISEASES
862  |  RUNX1T1  |  DISEASES
5087  |  PBX1  |  DISEASES
1408  |  CRY2  |  DISEASES
408  |  ARRB1  |  DISEASES
3077  |  HFE  |  DISEASES
9774  |  BCLAF1  |  DISEASES
930  |  CD19  |  DISEASES
7786  |  MAP3K12  |  DISEASES
Locus(Waiting for update.)
Disease ID 1751
Disease childhood leukemia
Integrated Phenotype(Waiting for update.)
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:5)
HP:0010885  |  Aseptic necrosis  |  2
HP:0000096  |  Glomerulosclerosis  |  1
HP:0001903  |  Anemia  |  1
HP:0001909  |  Leukemia  |  1
HP:0000097  |  focal glomerulosclerosis  |  1
Disease ID 1751
Disease childhood leukemia
Manually Symptom(Waiting for update.)
Text Mined Symptom
UMLS | Name | Sentences' Count(Total Symptoms:1)
C0009450  |  infection  |  1
Manually Genotype(Total Text Mining Genotypes:0)
(Waiting for update.)
All Snps(Total Genotypes:11)
snpId pubmedId geneId geneSymbol diseaseId sourceId sentence score Year geneSymbol_dbSNP CHROMOSOME POS REF ALT
rs10508293183396824524MTHFRumls:C1332977BeFreeThe maternal methylenetetrahydrofolate reductase A1298C polymorphism was found to be an effect modifier of the maternal intron 4 polymorphism of the AKR1C3 gene (rs10508293) and the childhood leukemia risk.0.0010857672008AKR1C3105098945AG
rs1695128276511555CYP2B6umls:C1332977BeFreeThe role of methylenetetrahydrofolate reductase (MTHFR C677T), glutathione S-transferases (GSTM1 and GSTT1 null, GSTP1 Ile105Val), and cytochromes p450 (CYP1A1*2A) genotypes in the etiology of childhood leukemia was simultaneously investigated.0.0002714422003GSTP11167585218AG
rs1695128276514524MTHFRumls:C1332977BeFreeThe role of methylenetetrahydrofolate reductase (MTHFR C677T), glutathione S-transferases (GSTM1 and GSTT1 null, GSTP1 Ile105Val), and cytochromes p450 (CYP1A1*2A) genotypes in the etiology of childhood leukemia was simultaneously investigated.0.0010857672003GSTP11167585218AG
rs1695128276512950GSTP1umls:C1332977BeFreeThe role of methylenetetrahydrofolate reductase (MTHFR C677T), glutathione S-transferases (GSTM1 and GSTT1 null, GSTP1 Ile105Val), and cytochromes p450 (CYP1A1*2A) genotypes in the etiology of childhood leukemia was simultaneously investigated.0.0002714422003GSTP11167585218AG
rs1695128276511543CYP1A1umls:C1332977BeFreeThe role of methylenetetrahydrofolate reductase (MTHFR C677T), glutathione S-transferases (GSTM1 and GSTT1 null, GSTP1 Ile105Val), and cytochromes p450 (CYP1A1*2A) genotypes in the etiology of childhood leukemia was simultaneously investigated.0.0013572092003GSTP11167585218AG
rs1695128276512952GSTT1umls:C1332977BeFreeThe role of methylenetetrahydrofolate reductase (MTHFR C677T), glutathione S-transferases (GSTM1 and GSTT1 null, GSTP1 Ile105Val), and cytochromes p450 (CYP1A1*2A) genotypes in the etiology of childhood leukemia was simultaneously investigated.0.0005428842003GSTP11167585218AG
rs1695128276512944GSTM1umls:C1332977BeFreeThe role of methylenetetrahydrofolate reductase (MTHFR C677T), glutathione S-transferases (GSTM1 and GSTT1 null, GSTP1 Ile105Val), and cytochromes p450 (CYP1A1*2A) genotypes in the etiology of childhood leukemia was simultaneously investigated.0.0002714422003GSTP11167585218AG
rs370216745210731321728NQO1umls:C1332977BeFreeOur results suggest that increased risk of infant leukemia development in patients with NQO1 *1*3 polymorphism is partially dependent on the inhibition of p53 pathway, though further studies are needed to fully understand the pathological role of C465T variant in the development of childhood leukemia.0.0008143262010TP53177674949AG
rs397507444183396824524MTHFRumls:C1332977BeFreeThe maternal methylenetetrahydrofolate reductase A1298C polymorphism was found to be an effect modifier of the maternal intron 4 polymorphism of the AKR1C3 gene (rs10508293) and the childhood leukemia risk.0.0010857672008MTHFR111794407TG
rs4925222939429446GSTO1umls:C1332977BeFreeThe polymorphism A140D of GSTO1-1 has been not only associated with distinct urinary profile of arsenic metabolites in populations chronically exposed to iAs in drinking water, but also with higher risk of childhood leukemia and lung disease in non-exposed populations, suggesting that GSTO1-1 involvement in other physiologic processes different from toxics metabolism could be more relevant than is thought.0.0002714422012GSTO110104263031CA
rs854560229768395444PON1umls:C1332977BeFreePON1 rs854560 (L55M) was associated with an increased risk of developing childhood leukemia (LM + MM, OR 1.93, 95 % CI 1.32-2.81).0.0002714422012PON1795316772AC,G,N,T
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.)