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  3. IMMUNODEFICIENCY, COMMON VARIABLE, 2; CVID2

Immunodeficiency, Common Variable, 2; Cvid2

Table of contents:

Genes related to Immunodeficiency, Common Variable, 2; Cvid2

  • TNFRSF13B

View recommended genes panels

Clinical Features

Top most frequent phenotypes and symptoms related to Immunodeficiency, Common Variable, 2; Cvid2

  • Neoplasm
  • Hepatomegaly
  • Diarrhea
  • Splenomegaly
  • Immunodeficiency
  • Recurrent infections
  • Carcinoma
  • Autoimmunity
  • Lymphoma
  • Decreased antibody level in blood

And another 17 symptoms. If you need more information about this disease we can help you.

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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

Immunodeficiency, Common Variable, 2; Cvid2 Is also known as antibody deficiency due to taci defect, hypogammaglobulinemia due to taci deficiency.

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, Common Variable, 2; Cvid2 Recommended genes panels

Panel Name, Specifity and genes Tested/covered
Common Variable Immunodeficiency Syndrome (CVID): TNFRSF13B (TACI) (Full Gene Sequencing).

By Molecular Diagnostic Laboratory University of Alberta (Canada).

TNFRSF13B
Specificity
100 %
Genes
100 %
Common Variable Immunodeficiency Syndrome (CVID): TNFRSF13B (TACI) (Known Mutation).

By Molecular Diagnostic Laboratory University of Alberta (Canada).

TNFRSF13B
Specificity
100 %
Genes
100 %
TNFRSF13B Sequencing.

By Cincinnati Children's Hospital Medical Center Laboratory of Genetics and Genomics Cincinnati Children's Hospital Medical Center (United States).

TNFRSF13B
Specificity
100 %
Genes
100 %
TNFRSF13B Deletion/duplication analysis.

By Cincinnati Children's Hospital Medical Center Laboratory of Genetics and Genomics Cincinnati Children's Hospital Medical Center (United States).

TNFRSF13B
Specificity
100 %
Genes
100 %
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 %
Primary Antibody Deficiency Panel, Sequencing and Deletion/Duplication.

By ARUP Laboratories, Molecular Genetics and Genomics (United States).

SH2D1A, BTK, CD40, CD40LG, UNG, VAV1, AICDA, BLNK, CD19, CD79A, CD79B, CD81, LRBA, TNFRSF13C, TNFRSF13B, ADA, LRRC8A, CR2, ICOS, IGHM , (...)

View the complete list with 15 more genes
Specificity
3 %
Genes
100 %
TACI-Associated Common Variable Immunodeficiency (TNFRSF13B) Sequencing.

By ARUP Laboratories, Molecular Genetics and Genomics (United States).

TNFRSF13B
Specificity
100 %
Genes
100 %
Immunoglobulin A deficiency (sequence analysis of TNFRSF13B gene).

By CGC Genetics (Portugal).

TNFRSF13B
Specificity
100 %
Genes
100 %

You can get up to 22 more panels with our dedicated tool

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Sources and references

You can check the following sources for additional information.

OMIM Rare Disease Symptoms Checker

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