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Spinocerebellar ataxia type 19/22

Just diagnosed with Spinocerebellar ataxia type 19/22?

You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Spinocerebellar ataxia type 19/22, look for clinical trials, and connect with others living with it — all in one place.

Open the full Spinocerebellar ataxia type 19/22 hub →

Overview

Spinocerebellar ataxia type 19/22 is a rare condition. Also known as SCA19/22. Tomeko brings together the specialists, research, clinical trials, treatments and community for Spinocerebellar ataxia type 19/22 so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.

Identifiers: ORPHA:98772 · OMIM 607346 · ICD-10 G11.2 · GARD 0012365

Find care for Spinocerebellar ataxia type 19/22

Authoritative references for Spinocerebellar ataxia type 19/22

Common questions

I was just diagnosed with Spinocerebellar ataxia type 19/22 — what should I do first?

Start by learning the basics from an authoritative source, find a specialist or center that sees Spinocerebellar ataxia type 19/22, and connect with a patient organization. Tomeko brings these together on one hub.

Where can I find a specialist for Spinocerebellar ataxia type 19/22?

Use Tomeko's specialist and Centers-of-Excellence directories to find clinicians who treat Spinocerebellar ataxia type 19/22, filtered to your area.

Are there clinical trials for Spinocerebellar ataxia type 19/22?

Tomeko shows live, recruiting studies for Spinocerebellar ataxia type 19/22 from ClinicalTrials.gov on the hub.

Informational only — not medical advice. Always consult a qualified clinician. Provider and reference data from public sources (NIH GARD, Orphanet, OMIM, HPO, MONDO, ClinicalTrials.gov, CMS NPPES). © Tomeko · tomekohealth.com