You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 1, look for clinical trials, and connect with others living with it — all in one place.
Open the full Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 1 hub →Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 1 is a rare condition. Also known as SCAN1. Tomeko brings together the specialists, research, clinical trials, treatments and community for Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 1 so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:94124 · OMIM 607250 · ICD-10 G60.2 · GARD 0010000
Start by learning the basics from an authoritative source, find a specialist or center that sees Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 1, 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, with axonal neuropathy 1, filtered to your area.
Tomeko shows live, recruiting studies for Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 1 from ClinicalTrials.gov on the hub.