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Living with Dianzani autoimmune lymphoproliferative disease

A very rare immune condition with autoimmunity and swollen lymph nodes or spleen.

Understanding Dianzani autoimmune lymphoproliferative disease

Dianzani autoimmune lymphoproliferative disease (DALD) is a very rare condition marked by autoimmunity, swollen lymph nodes, and an enlarged spleen.

Autoimmunity means the immune system attacks the body's own tissue. GARD lists onset any time in life.

Signs & symptoms

GARD doesn't list a symptom list. Based on its summary, features include:

  • Autoimmunity (the immune system attacking the body)
  • Swollen lymph nodes
  • Enlarged spleen

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

    Specialists who may be involved include allergy and immune system specialists, cancer specialists and genetic specialists.

  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
Allergy and immune system specialists (allergists / immunologists); Cancer specialists (oncologists); Genetic specialists (geneticists)
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
Which tests confirm Dianzani autoimmune lymphoproliferative disease?
Which specialists, such as immunology, should follow my care?
Can genetic testing help our family?

Quick facts

Symptoms usually startany time in life

GARD says changes in genes cause this condition. It doesn't list a specific gene or inheritance pattern.

Genetic

Also known as: autoimmune lymphoproliferative syndrome without fas mutations; dald; dald - dianzani autoimmune lymphoproliferative disease; dianzani autoimmune lymphoproliferative syndrome; dianzani form of autoimmune lymphoproliferative disease

Patient organizations

Broader rare-disease groups

Source: NIH GARD · Dianzani autoimmune lymphoproliferative diseaseGARD ID 9797 · 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 Dianzani autoimmune lymphoproliferative disease.

Explore the Dianzani autoimmune lymphoproliferative disease blog

Explore research for Dianzani autoimmune lymphoproliferative disease

Explore actively recruiting Dianzani autoimmune lymphoproliferative disease studies with HealthSpark.

HealthSpark

Find actively recruiting studies for Dianzani autoimmune lymphoproliferative disease 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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