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Autosomal recessive spastic paraplegia type 76

Just diagnosed with Autosomal recessive spastic paraplegia type 76?

You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Autosomal recessive spastic paraplegia type 76, look for clinical trials, and connect with others living with it — all in one place.

Open the full Autosomal recessive spastic paraplegia type 76 hub →

Overview

Autosomal recessive spastic paraplegia type 76 is a rare condition. Also known as SPG76. Tomeko brings together the specialists, research, clinical trials, treatments and community for Autosomal recessive spastic paraplegia type 76 so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.

Identifiers: ORPHA:488594 · OMIM 616907 · ICD-10 G11.4 · GARD 0017892

Find care for Autosomal recessive spastic paraplegia type 76

Authoritative references for Autosomal recessive spastic paraplegia type 76

Common questions

I was just diagnosed with Autosomal recessive spastic paraplegia type 76 — what should I do first?

Start by learning the basics from an authoritative source, find a specialist or center that sees Autosomal recessive spastic paraplegia type 76, and connect with a patient organization. Tomeko brings these together on one hub.

Where can I find a specialist for Autosomal recessive spastic paraplegia type 76?

Use Tomeko's specialist and Centers-of-Excellence directories to find clinicians who treat Autosomal recessive spastic paraplegia type 76, filtered to your area.

Are there clinical trials for Autosomal recessive spastic paraplegia type 76?

Tomeko shows live, recruiting studies for Autosomal recessive spastic paraplegia type 76 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