The registry is a unique online tool that helps empower patients, families, clinicians and researchers to work together to improve the knowledge of these disorders. This knowledge has the potential to accelerate research for new treatments and improve care. The registry establishes a global resource of information gathered from patients and families like you who are affected by organic acidemias. The type of information collected will include diagnoses, symptoms, current treatments, and quality of life. This information is crucial to developing new treatments.