OUR MISSION
We’re committed to improving the lives of individuals affected by ATAD3A gene-related disorders, including Harel-Yoon Syndrome.
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We support groundbreaking scientific research, provide information and a support network for patients and families, and advocate for improved medical care.
Every person shown here lives with ATAD3A mutations. Their stories inspire, give hope and drive research.
What You Can Do
DONATE
Support ATAD3A
Patient Advocacy Alliance
Make a tax-deductible donation to fund research and support our mission.
PATIENT REGISTRY
Get Research-Ready with MitoSHARE
Please participate in the MitoSHARE registry to provide consistent data to researchers who are working to better understand ATAD3A mutations and how to treat them.
OUR PLANS
A Support Community for ATAD3A Conditions
We support groundbreaking scientific research, provide information and a support network for patients and families, and advocate for improved medical care
Patient and Family Support
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​Create a welcoming, informed, and connected experience for newly diagnosed families.
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Treatment Advancement
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Support progress toward a treatment that improves quality of life.​
Clinician and Researcher Engagement
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Increase collaboration, interest, and knowledge among researchers and clinicians.
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Informational Resources
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Provide accurate, accessible educational content.
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Early Detection and Diagnosis
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Improve identification of new ATAD3A cases.