Forms and Documents
- Confirmation of clinical diagnosis in symptomatic patients
- Genetic counseling and risk assessment of asymptomatic family members of a proband with HCM
- Differentiation of hereditary HCM associated with mutations in sarcomeric genes from phenocopies (i.e. Danon disease, Fabry disease, Noonan syndrome, Pompe disease, Amyloidosis)
- Deletion/Duplication Analysis
- Next-Gen Sequencing
*Reporting times are typical, but could be extended in situations outside GeneDx's reasonable control.
**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.