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Living with Immunoglobulin A deficiency 2

A selective IgA deficiency caused by changes in the TNFRSF13B gene.

Understanding Immunoglobulin A deficiency 2

Immunoglobulin A deficiency 2 is a selective IgA deficiency disease caused by a change in the TNFRSF13B gene.

GARD doesn't give more details for this condition yet. Its description is that it is a selective IgA deficiency (low IgA, an antibody) caused by a mutation in the TNFRSF13B gene.

Signs & symptoms

GARD doesn't list specific symptoms for this condition yet.

Not everyone has every symptom. GARD's list comes from the Human Phenotype Ontology.

Diagnosis

  1. Talk with your doctor

    Share the symptoms you've noticed, when they started and your family health history. Notes and photos can help.

  2. See a specialist

    Your doctor may refer you to a specialist who knows rare conditions.

  3. Ask which tests can help

    Your care team will decide which exams and tests can confirm the diagnosis.

  4. Connect with expert centers

    Immune Deficiency Foundation may keep lists of experts for this condition.

Care & treatment

Care team
A doctor familiar with rare conditions, plus specialists as needed
Expert care
Expert lists: Immune Deficiency Foundation
Treatment
GARD doesn't list specific treatments for this condition. Your care team will tailor care to your symptoms.
Research
Clinical trials and observational studies may be options. See the research section below.

General information, not medical advice. Your care team makes the decisions.

Everyday life

Living with a rare condition is easier with support.

  • Connect with Immune Deficiency Foundation
  • Keep notes on symptoms, changes and questions for appointments
  • Ask about patient registries that help research
  • Look into financial aid and travel resources for care visits
Bring these questions to your next doctor visit
Can genetic testing for the TNFRSF13B gene confirm the diagnosis?
How is my IgA level checked?
What signs of infection should I watch for?

Quick facts

GARD says the disease is caused by a mutation in the TNFRSF13B gene.

Also known as: igad2; immunoglobulin a deficiency type 2; selective iga deficiency disease caused by mutation in tnfrsf13b; tnfrsf13b selective iga deficiency disease

Patient organizations

Source: NIH GARD · Immunoglobulin A deficiency 2GARD ID 10198 · GARD page updated September 2026 · Plain-language summary by Know Rare; editorial review pending. General information, not medical advice.

You are more than your diagnosis

Perspectives from people navigating life with Immunoglobulin A deficiency 2.

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Explore research for Immunoglobulin A deficiency 2

Explore actively recruiting Immunoglobulin A deficiency 2 studies with HealthSpark.

HealthSpark

Find actively recruiting studies for Immunoglobulin A deficiency 2 with HealthSpark. Share your city to explore research near you.

  • Recruiting studies from ClinicalTrials.gov
  • Share your city to look for research near you
  • Eligibility is confirmed by the study team

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Powered by HealthSpark, our AI chat helper · Study information from ClinicalTrials.gov · Eligibility is confirmed by the study team.

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