Benta Disease

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.

Alternative names

Benta Disease Is also known as b-cell expansion with nf-kb and t-cell anergy disease.

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.


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Benta Disease Recommended genes panels

Panel Name, Specifity and genes Tested/covered
Tier 2: Hereditary Lymphoma and Immunodeficiency Panel.

By Genetic Services Laboratory University of Chicago (United States).

BLM, SH2D1A, BRCA1, BRCA2, STXBP2, FAS, CD27, FASLG, WAS, IKZF1, CASP10, CARD11, TNFRSF13B, ADA, DOCK8, CTLA4, MAGT1, ITK, NBN, NF1 , (...)

View the complete list with 3 more genes
Specificity
5 %
Genes
100 %
CentoICU platinum plus.

By Centogene AG - the Rare Disease Company (Germany).

RMRP, BCS1L, BDNF, RPS19, RPS6KA3, SALL1, SCN1A, SCN2A, SFTPB, SFTPC, SFTPD, ST3GAL5, STIL, SIX1, SIX5, SLC16A1, SLCO1B1, SLCO1B3, SLC22A5, BRAF , (...)

View the complete list with 487 more genes
Specificity
1 %
Genes
100 %
New Born testing (CentoICU).

By Centogene AG - the Rare Disease Company (Germany).

RMRP, BCS1L, BDNF, RPS19, RPS6KA3, SALL1, SCN1A, SCN2A, SFTPB, SFTPC, SFTPD, ST3GAL5, STIL, SIX1, SIX5, SLC16A1, SLCO1B1, SLCO1B3, SLC22A5, BRAF , (...)

View the complete list with 487 more genes
Specificity
1 %
Genes
100 %
B-cell expansion with NFKB and T-cell anergy.

By Centogene AG - the Rare Disease Company (Germany).

CARD11
Specificity
100 %
Genes
100 %
Immunodeficiency type 11.

By Centogene AG - the Rare Disease Company (Germany).

CARD11
Specificity
100 %
Genes
100 %
Immune dysregulation Panel.

By CeGaT GmbH (Germany).

SH2D1A, STX11, STXBP2, FAS, FASLG, TREX1, ITCH, CASP10, CASP8, CARD11, LYST, UNC13D, AIRE, FCGR2B, AOAH, AP3B1, XIAP, IL2RA, FOXP3, PRF1 , (...)

View the complete list with 2 more genes
Specificity
5 %
Genes
100 %
Combined immunodeficiencies Panel.

By CeGaT GmbH (Germany).

RMRP, SEMA3E, STAT5B, STIM1, STK4, TAPBP, TBX1, THBD, TNFRSF4, CD40, CD27, CD40LG, TRAC, ACP5, FOXN1, ZAP70, CARD11, CD3D, CD3E, CD3G , (...)

View the complete list with 39 more genes
Specificity
2 %
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
Specificity
3 %
Genes
100 %

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Sources and references

You can check the following sources for additional information.

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 WEBB-DATTANI SYNDROME; WEDAS TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 1; HHT1 MAZABRAUD SYNDROME CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2W; CMT2W ISOLATED BRACHYCEPHALY

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