General Information of Disease (ID: DISGYV3F)

Disease Name Lymphosarcoma
Synonyms malignant lymphoma (category); diffuse lymphoma; lymphosarcoma
Definition An antiquated term that refers to a non-Hodgkin lymphoma composed of small and medium sized lymphocytes.
Disease Hierarchy
DISUX76L: Lymphatic system cancer
DISS2Y8A: Non-hodgkin lymphoma
DISGYV3F: Lymphosarcoma
Disease Identifiers
MONDO ID
MONDO_0004638
MESH ID
D008228
UMLS CUI
C3714542
MedGen ID
811370
SNOMED CT ID
188498009

Drug-Interaction Atlas (DIA) of This Disease

Drug-Interaction Atlas (DIA)
This Disease is Treated as An Indication in 1 Approved Drug(s)
Drug Name Drug ID Highest Status Drug Type REF
Rituximab DM1YVZT Approved Antibody [1]
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Molecular Interaction Atlas (MIA) of This Disease

Molecular Interaction Atlas (MIA)
This Disease Is Related to 8 DTT Molecule(s)
Gene Name DTT ID Evidence Level Mode of Inheritance REF
TFRC TT8MG4S Limited Biomarker [2]
TYMS TTP1UKZ moderate Biomarker [3]
CBS TTVZJ7G Strong Biomarker [4]
CHEK2 TT9ABMF Strong Biomarker [5]
CSF2 TTNYZG2 Strong Therapeutic [6]
CYP2E1 TTWVHQ5 Strong Biomarker [7]
HLA-DRB1 TTUXSTW Strong Biomarker [8]
BCL6 TTC9YX5 Definitive Biomarker [9]
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⏷ Show the Full List of 8 DTT(s)
This Disease Is Related to 2 DME Molecule(s)
Gene Name DME ID Evidence Level Mode of Inheritance REF
EPHX1 DELB4KP Strong Biomarker [7]
FPGS DECWT2V Strong Biomarker [4]
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This Disease Is Related to 9 DOT Molecule(s)
Gene Name DOT ID Evidence Level Mode of Inheritance REF
ALG1 OTVXPA9E Strong Posttranslational Modification [10]
BHMT OTYB6PXZ Strong Biomarker [4]
CHIC2 OTNE3T6Z Strong Genetic Variation [11]
MT1F OTZVUYG1 Strong Posttranslational Modification [10]
MT1G OTAV1OCR Strong Posttranslational Modification [10]
MT1H OT0MVBM6 Strong Posttranslational Modification [10]
MT1M OTVT8PLU Strong Posttranslational Modification [10]
MT1X OT9AKFVS Strong Posttranslational Modification [10]
SHMT1 OTIINA3J Strong Biomarker [4]
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⏷ Show the Full List of 9 DOT(s)

References

1 Infusion reactions associated with the therapeutic use of monoclonal antibodies in the treatment of malignancy. Cancer Metastasis Rev. 1999;18(4):465-71.
2 The transferrin receptor part I: Biology and targeting with cytotoxic antibodies for the treatment of cancer.Clin Immunol. 2006 Nov;121(2):144-58. doi: 10.1016/j.clim.2006.06.010. Epub 2006 Aug 10.
3 Risk of non-Hodgkin lymphoma associated with polymorphisms in folate-metabolizing genes.Cancer Epidemiol Biomarkers Prev. 2005 Dec;14(12):2999-3003. doi: 10.1158/1055-9965.EPI-05-0515.
4 Gene-nutrient interactions among determinants of folate and one-carbon metabolism on the risk of non-Hodgkin lymphoma: NCI-SEER case-control study.Blood. 2007 Apr 1;109(7):3050-9. doi: 10.1182/blood-2006-07-034330.
5 Association of Germline CHEK2 Gene Variants with Risk and Prognosis of Non-Hodgkin Lymphoma.PLoS One. 2015 Oct 27;10(10):e0140819. doi: 10.1371/journal.pone.0140819. eCollection 2015.
6 DICE (dexamethasone, ifosfamide, cisplatin, etoposide) infusional chemotherapy for refractory or relapsed non-Hodgkin's lymphoma (NHL).Eur J Haematol Suppl. 2001 Jul;64:41-5.
7 Genetic polymorphisms of biotransformation enzymes in patients with Hodgkin's and non-Hodgkin's lymphomas.Hum Mol Genet. 2001 Jun 1;10(12):1265-73. doi: 10.1093/hmg/10.12.1265.
8 Variation in effects of non-Hodgkin lymphoma risk factors according to the human leukocyte antigen (HLA)-DRB1*01:01 allele and ancestral haplotype 8.1.PLoS One. 2011;6(11):e26949. doi: 10.1371/journal.pone.0026949. Epub 2011 Nov 9.
9 Suppression of human B cell activation by 2,3,7,8-tetrachlorodibenzo-p-dioxin involves altered regulation of B cell lymphoma-6.Toxicol Sci. 2015 Mar;144(1):39-50. doi: 10.1093/toxsci/kfu257. Epub 2014 Dec 26.
10 Physical and functional interaction of DNA methyltransferase 3A with Mbd3 and Brg1 in mouse lymphosarcoma cells.Cancer Res. 2005 Dec 1;65(23):10891-900. doi: 10.1158/0008-5472.CAN-05-1455.
11 Characterization of differentially expressed genes in the bovine T lymphoma cell line.Vet Immunol Immunopathol. 1998 Apr 16;62(3):209-19. doi: 10.1016/s0165-2427(98)00098-1.