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 Medical Provider brochure offers a general overview of CACNA1A-related disorders specifically geared toward clinicians.

• We have specific resources available for clinicians on Hemiplegic Migraines.

• We facilitate patient’s engagement in research studies as it is a crucial means of expanding our understanding of CACNA1A-related disorders and expediting the development of future treatments and therapies. We want to move research forward but we need to find patients - please send your patients to us! You can read more here.

• Our Creating Connections Community Conference (7/9 - 7/11) is a great way to learn more about CACNA1A-related disorders and connect with other clinicians. For more information and to register, click here.

• Want to join our list of recommended providers? Register here.

• More resources are below to share with your patients about CACNA1A-related disorders so they can be better informed.

Have any questions?

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