Immunodeficiency 37; Imd37

Table of contents:

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

Genes related to Immunodeficiency 37; Imd37

BCL10

View recommended genes panels

Clinical Features

Phenotypes and symptoms related to Immunodeficiency 37; Imd37

Seizures
Immunodeficiency
Recurrent infections
Respiratory tract infection
Decreased antibody level in blood
Status epilepticus
Progressive neurologic deterioration
Lymphopenia
Encephalitis
Combined immunodeficiency

Incidence and onset information

— Currently we don't have prevalence information about this disease (Not enough data available about incidence and published cases.)
— No data available about the known clinical features onset.

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.

Immunodeficiency 37; Imd37 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 Genetic Syndrome Finder

If you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like SESSILE SERRATED POLYPOSIS CANCER SYNDROME; SSPCS ATAXIA-OCULOMOTOR APRAXIA 3; AOA3 CHROMOSOME 15q13.3 DELETION SYNDROME CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ih; CDG1H KEPPEN-LUBINSKY SYNDROME; KPLBS