Hereditary Multigene Panel for Blood Disorders (Electrophoresis-Based Screening)
This test checks for genetic variations linked to inherited blood conditions, including conditions affecting red blood cells, hemoglobin, or enzymes that may cause anemia or other blood-related issues.
["Identifying potential genetic causes of blood disorders that may require further medical evaluation or treatment."]
Key facts at a glance
- LOINC
- 105259-6
- Short code
- Hereditary multigene anl Bld/T
- Synonyms
- Hereditary multigene anl 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
- 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 multiple genes associated with hereditary blood disorders. It may detect mutations in genes linked to conditions such as sickle cell disease, thalassemia, or other hemoglobinopathies, or in genes affecting red blood cell structure or function.
How the Test Works
This screening uses electrophoresis, a method that separates different blood components based on size and charge. It helps identify abnormal proteins or genetic markers that may indicate inherited blood disorders.
Why It Might Be Ordered
Your healthcare provider may recommend this test if you have a family history of blood disorders, symptoms like fatigue, pale skin, or unusual bruising, or if you are planning pregnancy and there is a risk of hereditary conditions.
Sample Collection and Preparation
A blood sample is typically drawn from a vein in your arm. The sample is processed to isolate specific components for analysis. No special preparation is needed, but fasting may not be required unless specified by your provider.
Clinical interpretation
How abnormal results are interpreted and what conditions they suggest.
◆Associated findings1
Short name
Multigene Blood Disorder Screen
Frequently asked questions
Identifying genetic variations early can help guide treatment options, family planning advice, or preventive measures. Some conditions may require monitoring, lifestyle adjustments, or specialized care to manage symptoms effectively.
What does a positive result mean?
How long does it take to get results?
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