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Spinocerebellar ataxia type 29

Just diagnosed with Spinocerebellar ataxia type 29?

You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Spinocerebellar ataxia type 29, look for clinical trials, and connect with others living with it — all in one place.

Open the full Spinocerebellar ataxia type 29 hub →

Overview

Spinocerebellar ataxia type 29 is a rare condition. Also known as Congenital nonprogressive spinocerebellar ataxia, SCA29. Tomeko brings together the specialists, research, clinical trials, treatments and community for Spinocerebellar ataxia type 29 so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.

Identifiers: ORPHA:208513 · OMIM 117360 · ICD-10 G11.0 · GARD 0010480

Find care for Spinocerebellar ataxia type 29

Authoritative references for Spinocerebellar ataxia type 29

Common questions

I was just diagnosed with Spinocerebellar ataxia type 29 — what should I do first?

Start by learning the basics from an authoritative source, find a specialist or center that sees Spinocerebellar ataxia type 29, and connect with a patient organization. Tomeko brings these together on one hub.

Where can I find a specialist for Spinocerebellar ataxia type 29?

Use Tomeko's specialist and Centers-of-Excellence directories to find clinicians who treat Spinocerebellar ataxia type 29, filtered to your area.

Are there clinical trials for Spinocerebellar ataxia type 29?

Tomeko shows live, recruiting studies for Spinocerebellar ataxia type 29 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