: Hereditary Sensory and Autonomic Neuropathy Multi-Gene Panel, Blood
: This test analyzes multiple genes from a blood sample to look for genetic changes associated with hereditary sensory and autonomic neuropathies, a group of rare inherited nerve disorders.
[": The panel helps identify genetic causes of inherited sensory and autonomic nerve problems using a single blood draw."]
Key facts at a glance
- LOINC
- 103729-0
- Short code
- Hrd sens neur multi Bld/T
- Synonyms
- Hrd sens neur multi 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 Looks At
: Hereditary sensory and autonomic neuropathies (HSAN) are a group of rare inherited conditions that affect the nerves carrying sensation and controlling automatic body functions. This multi-gene panel examines several genes at once to look for variants that may cause these disorders.
: Why It May Be Ordered
: A healthcare provider may order this panel when a person has symptoms suggesting an inherited nerve disorder, such as reduced pain or temperature sensation, autonomic symptoms, or a family history of similar problems. Genetic testing can help clarify the cause and guide family discussions.
: How the Sample Is Collected
: The test is performed on a blood sample collected in a standard draw. No special preparation is usually required, though your provider will give specific instructions if needed.
: Understanding Possible Results
: Results may identify a genetic variant that explains symptoms, a variant of uncertain significance whose effect is unclear, or no relevant variant. Because interpretation depends on the specific genes and variants examined, results should always be reviewed with a genetics professional or your care team.
Clinical interpretation
How abnormal results are interpreted and what conditions they suggest.
: Identifying a genetic cause can support accurate diagnosis, inform management and monitoring, and help relatives decide whether testing is appropriate for them. Because HSAN conditions are rare and genetic variants can be complex, results require careful interpretation in the context of symptoms and family history.
Short name
: HSAN Genetic Panel
Frequently asked questions
: Is this test used to diagnose a nerve problem?
: Does a normal result rule out all nerve disorders?
: Will I need genetic counseling?
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