Combined Immunodeficiency Multigene Analysis (Whole Blood DNA)
This test examines genetic variations across multiple genes linked to primary immunodeficiency disorders, helping identify potential causes of weakened immune function.
["A genetic check for rare immune system disorders that may affect your health or increase infection risk."]
Key facts at a glance
- LOINC
- 112329-8
- Short code
- Combined immunodeficiency multigene analysis Bld/T
- Synonyms
- Combined immunodeficiency multigene analysis Bld/T
- Category
- chemistry
- Sample
- whole-blood
- Container
- Lavender-top (EDTA)
- Units
- N/A
- Fasting
- false
- Population
- adult
- Sex
- all
- Age range
- 18–65 years
- Method
- molgen
- CPT
- 86038
- Specimen volume
- 3 mL
- Stability
- Room temperature: 4h, Refrigerated: 24h
- Hemolysis max
- 0
- Lipemia max
- 0
- Icterus max
- 0
- TAT
- 4–24 hours
- Order
- routine
What This Test Measures
The test analyzes DNA from your blood to detect specific mutations in genes associated with primary immunodeficiencies. These mutations can impair immune cell development or function, leading to recurrent infections, chronic inflammation, or other immune-related symptoms. Some genes may also be linked to autoimmune conditions or cancer risk.
Why It Might Be Ordered
Your healthcare provider may recommend this test if you have symptoms like frequent, severe infections (e.g., pneumonia, sinusitis, or skin infections), unusual allergic reactions, or a family history of immunodeficiency. It’s also used in newborn screening programs or for diagnosing suspected inherited immune disorders.
Sample Collection and Process
A blood sample is drawn from your arm, and DNA is extracted from your white blood cells. The lab then sequences DNA from multiple genes to identify any inherited changes that could affect immunity. Results are compared to a reference database of known genetic variations.
What to Expect After Testing
Results typically take 4–8 weeks. If abnormalities are found, your doctor will discuss next steps, which may include additional testing, monitoring, or genetic counseling. Follow-up may involve managing symptoms, lifestyle adjustments, or specialized treatments if applicable.
Clinical interpretation
How abnormal results are interpreted and what conditions they suggest.
◆Associated findings1
Short name
Multigene Panel for Immunodeficiency
Frequently asked questions
How can I prepare for this test?
What does a positive result mean?
Will this test affect my insurance or coverage?
Sources
- 1
- 2Lab Tests OnlineSource
- 3
Click any link to access the full source. PubMed Central (PMC) links provide free full-text access.
This information is for educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment.
This content is for general informational and educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment. Always seek the guidance of a qualified healthcare provider with any questions you have about a medical condition, and never disregard professional medical advice or delay seeking it because of something you read here.
If you think you may have a medical emergency, call your local emergency number or go to the nearest emergency department immediately.
Medically reviewed by WellAlly Editorial Team Last reviewed August 16, 2026. · Read our editorial policy