Clinician Resources

Let’s Work Together

If you are treating someone with a CACNA1A-related disorder, we ask you to please connect the family to the CACNA1A Foundation. We are a global community and can provide resources & support to families affected by this rare, genetic disease. Additionally, we are supporting research and the more patients we have, the stronger we are!

• Our website provides information about CACNA1A-related disorders for your patients under Newly Diagnosed.

• Starting October 1, 2025 the ICD-10 code for CACNA1A-related neurodevelopmental disorder is QA0.0102.

• Educational webinars, archived on our website, deliver valuable information for patients, clinicians and researchers.

• Our Natural History Study is the best way to move research forward but we need to find patients - please send your patients to us! You can read more about the importance of signing up for the CACNA1A Natural History Study on this blog post.

• Our Scientific and Family Conference (7/24 - 7/25/21) is a great way to learn more about CACNA1A-related diseases and connect with other clinicians. For more information and to register, click here.

• Printable resources to give to your patients about CACNA1A so they can be better informed…

Have any questions? Want to join our list of recommended providers?

Please reach out by filling in the form or emailing us at info@cacna1a.org