Forms and Documents
Test Details
- Brown-Vialetto-Van Laere Syndrome
- Charcot Marie Tooth (CMT)
- CMT with Focal Segmental Glomerulosclerosis
- Congenital Insensitivity to Pain (CIP)
- Congenital Insensitivity to Pain with Anhidrosis
- Distal Hereditary Motor Neuropathy
- Fabry Disease
- Familial Dysautonomia
- Familial Transthyretin Amyloidosis
- Hereditary Motor and Sensory Neuropathy (HMSN)
- Hereditary Sensory and Autonomic Neuropathy (HSAN)
- HSAN with Spastic Paraplegia
- Inherited Erythromelalgia (IEM)
- Menkes Disease
- Occipital Horn Disease
- Paroxysmal Extreme Pain Disorder (PEPD)
- Riley Day Syndrome
- Rosenberg-Chutorian Syndrome
- Small Fiber Neuropathy (SFN)
- Spinal Muscular Atrophy with Respiratory Distress Type 1 (SMARD1)
- Molecular confirmation of a clinical diagnosis
- To assist with decisions about treatment and management of individuals with neuropathy
- Testing of at-risk relatives for specific known mutation(s) previously identified in an affected family member
- Prenatal diagnosis for known familial mutation(s) in at-risk pregnancies
Ordering
*Reporting times are typical, but could be extended in situations outside GeneDx's reasonable control.
Billing
**The CPT codes provided are based on AMA guidelines and are for informational purposes only. CPT coding is the sole responsibility of the billing party. Please direct any questions regarding coding to the payer being billed.