You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Spinocerebellar ataxia, autosomal recessive 23, look for clinical trials, and connect with others living with it — all in one place.
Open the full Spinocerebellar ataxia, autosomal recessive 23 hub →Spinocerebellar ataxia, autosomal recessive 23 is a rare condition. Also known as SCAR23, Spinocerebellar ataxia autosomal recessive type 23. Tomeko brings together the specialists, research, clinical trials, treatments and community for Spinocerebellar ataxia, autosomal recessive 23 so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:404493 · OMIM 616949 · ICD-10 G11.1 · GARD 0017677
Start by learning the basics from an authoritative source, find a specialist or center that sees Spinocerebellar ataxia, autosomal recessive 23, and connect with a patient organization. Tomeko brings these together on one hub.
Use Tomeko's specialist and Centers-of-Excellence directories to find clinicians who treat Spinocerebellar ataxia, autosomal recessive 23, filtered to your area.
Tomeko shows live, recruiting studies for Spinocerebellar ataxia, autosomal recessive 23 from ClinicalTrials.gov on the hub.