Lymphoma, Mucosa-associated Lymphoid Type

Table of contents:

Description
Related genes
Clinical Features
Incidence and onset information
Alternative Names
Researches and researchers
Gene Panels
Sources and references

Description

The concept of mucosa-associated lymphoid tissue (MALT) lymphomas was introduced by Isaacson and Wright (1983). MALT lymphomas are now recognized as a distinct subtype of non-Hodgkin lymphoma (OMIM ). B-cell lymphomas of mucosa-associated lymphoid tissue (MALT lymphomas) are the most common form of lymphoma arising in extranodal sites, in most cases arising in the gastric mucosa (Isaacson and Spencer, 1995).

Genes related to Lymphoma, Mucosa-associated Lymphoid Type

BCL10

View recommended genes panels

Clinical Features

Phenotypes and symptoms related to Lymphoma, Mucosa-associated Lymphoid Type

Neoplasm
Immunodeficiency
Lymphoma
Hodgkin lymphoma
Gastric ulcer
Gastric lymphoma

Incidence and onset information

— Based on the latest data available LYMPHOMA, MUCOSA-ASSOCIATED LYMPHOID TYPE have a estimated prevalence of 7 per 100k worldwide.
— No data available about the known clinical features onset.

Alternative names

Lymphoma, Mucosa-associated Lymphoid Type Is also known as malt lymphoma, gastric lymphoma, primary.

Researches and researchers

Currently, we don't have any information about doctors, researches or researchers related to this disease. Please contact us if you would like to appear here.

Lymphoma, Mucosa-associated Lymphoid Type Recommended genes panels

Panel Name, Specifity and genes Tested/covered
Mesothelioma, somatic. By Centogene AG - the Rare Disease Company (Germany). BCL10 Specificity 100 % Genes 100 %
Lymphoma, MALT, somatic. By Centogene AG - the Rare Disease Company (Germany). BCL10 Specificity 100 % Genes 100 %
Lymphoma, follicular, somatic. By Centogene AG - the Rare Disease Company (Germany). BCL10 Specificity 100 % Genes 100 %
Male germ cell tumor, somatic. By Centogene AG - the Rare Disease Company (Germany). BCL10 Specificity 100 % Genes 100 %
Invitae Comprehensive Severe Combined Immunodeficiency (SCID) and Combined Immunodeficiency (CID) Panel. By Invitae (United States). STK4, TAPBP, TNFRSF4, CD27, CD40LG, ZAP70, CARD11, CD3D, CD3E, CD3G, CD247, CD8A, LRBA, DCLRE1C, ADA, DOCK8, CORO1A, CTPS1, NHEJ1, MAGT1 , (...) View the complete list with 29 more genes Panel complete gene list STK4, TAPBP, TNFRSF4, CD27, CD40LG, ZAP70, CARD11, CD3D, CD3E, CD3G, CD247, CD8A, LRBA, DCLRE1C, ADA, DOCK8, CORO1A, CTPS1, NHEJ1, MAGT1, DOCK2, AK2, TAP1, TAP2, ICOS, IKBKB, IL21, IL21R, IL2RG, IL7R, ITK, JAK3, LCK, LIG4, MALT1, MAP3K14, RHOH, CIITA, PNP, B2M, PRKDC, PTPRC, RAC2, RAG1, RAG2, BCL10, RFX5, RFXANK, RFXAP Specificity 3 % Genes 100 %
Invitae Primary Immunodeficiency Panel. By Invitae (United States). RMRP, RORC, SEMA3E, SH2D1A, SH3BP2, SLC7A7, SMARCAL1, BTK, STAT1, STAT2, STAT3, STAT5B, STIM1, STK4, STX11, STXBP2, TAPBP, TAZ, TBK1, TCN2 , (...) View the complete list with 187 more genes Panel complete gene list RMRP, RORC, SEMA3E, SH2D1A, SH3BP2, SLC7A7, SMARCAL1, BTK, STAT1, STAT2, STAT3, STAT5B, STIM1, STK4, STX11, STXBP2, TAPBP, TAZ, TBK1, TCN2, TERC, TERT, TINF2, TLR3, TNFRSF1A, TNFRSF4, FAS, CD27, TNFSF12, CD40LG, FASLG, TPP2, TRAF3, TREX1, ACP5, TYK2, UNG, WAS, WIPF1, FOXN1, ZAP70, ACTB, AICDA, TRAF3IP2, UNC93B1, ITCH, BLNK, NHP2, NOP10, LPIN2, VPS45, CASP10, CASP8, SPINK5, IL36RN, RBCK1, RTEL1, SAMHD1, CARD9, CARD11, NLRP3, IL17F, NLRC4, CARD14, CD3D, CD3E, CD3G, CD247, HAX1, CD79A, CD79B, CD8A, TRNT1, LRBA, DCLRE1B, DCLRE1C, TNFRSF13C, IRAK4, TMC6, TNFRSF13B, TICAM1, IL17RC, CEBPE, ADA2, RNASEH2A, ADA, IFIH1, DOCK8, ADAM17, LYST, TTC7A, SLC35C1, TMC8, CHD7, ZBTB24, VPS13B, COPA, ADAR, CORO1A, NLRP12, SLC29A3, UNC13D, FERMT3, CR2, RNASEH2C, CSF2RA, CSF3R, G6PC3, MOGS, CTLA4, ACD, CTPS1, CTSC, CXCR4, RNASEH2B, NHEJ1, CYBA, CYBB, ORAI1, CTC1, JAGN1, TMEM173, MAGT1, DKC1, EPG5, DNMT3B, LAMTOR2, DOCK2, CLPB, ELANE, FADD, AIRE, AK2, FPR1, ISG15, SLC37A4, GATA2, GFI1, TAP1, TAP2, NOD2, ICOS, IRF8, SP110, IFNGR1, IFNGR2, AP3B1, IGLL1, XIAP, IKBKB, IL10, IL10RA, IL10RB, IL12B, IL12RB1, IL17RA, IL1RN, IL21, IL21R, IL2RA, IL2RG, IL7R, FOXP3, IRF7, ITGB2, ITK, JAK3, LCK, LIG4, MALT1, MAP3K14, RHOH, MEFV, CIITA, MVK, MYD88, NBN, NCF2, NCF4, NFAT5, NFKB2, NFKBIA, PNP, ATM, BLOC1S6, PARN, PGM3, PIK3CD, PIK3R1, PLCG2, PMS2, B2M, POLE, PRF1, PRKCD, PRKDC, PSMB8, PSTPIP1, PTPRC, RAB27A, RAC2, RAG1, RAG2, BCL10, RFX5, RFXANK, RFXAP Specificity 1 % Genes 100 %
Invitae Combined Immunodeficiency (CID) Panel. By Invitae (United States). STK4, TAPBP, TNFRSF4, CD27, CD40LG, ZAP70, CARD11, CD3G, CD8A, LRBA, DOCK8, CTPS1, MAGT1, DOCK2, TAP1, TAP2, ICOS, IKBKB, IL21, IL21R , (...) View the complete list with 12 more genes Panel complete gene list STK4, TAPBP, TNFRSF4, CD27, CD40LG, ZAP70, CARD11, CD3G, CD8A, LRBA, DOCK8, CTPS1, MAGT1, DOCK2, TAP1, TAP2, ICOS, IKBKB, IL21, IL21R, ITK, LCK, MALT1, MAP3K14, RHOH, CIITA, B2M, RAC2, BCL10, RFX5, RFXANK, RFXAP Specificity 4 % Genes 100 %
BCL10. By Fulgent Genetics Fulgent Genetics (United States). BCL10 Specificity 100 % Genes 100 %

You can get up to 8 more panels with our dedicated tool

Learn more

Sources and references

You can check the following sources for additional information.

OMIM ORPHANET Rare Disease Search Engine

If you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like X-LINKED INTELLECTUAL DISABILITY, GOLABI-ITO-HALL TYPE DYSFIBRINOGENEMIA, CONGENITAL JUNCTIONAL EPIDERMOLYSIS BULLOSA, GENERALIZED SEVERE ISOLATED SCAPHOCEPHALY ACTH-INDEPENDENT MACRONODULAR ADRENAL HYPERPLASIA 2; AIMAH2