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Hereditary spastic paraplegia 36

Just diagnosed with Hereditary spastic paraplegia 36?

You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Hereditary spastic paraplegia 36, look for clinical trials, and connect with others living with it — all in one place.

Open the full Hereditary spastic paraplegia 36 hub →

Overview

Hereditary spastic paraplegia 36 is a rare condition. Also known as SPG36. Tomeko brings together the specialists, research, clinical trials, treatments and community for Hereditary spastic paraplegia 36 so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.

Identifiers: ORPHA:320365 · OMIM 613096 · ICD-10 G11.4 · GARD 0017472

Find care for Hereditary spastic paraplegia 36

Authoritative references for Hereditary spastic paraplegia 36

Common questions

I was just diagnosed with Hereditary spastic paraplegia 36 — what should I do first?

Start by learning the basics from an authoritative source, find a specialist or center that sees Hereditary spastic paraplegia 36, and connect with a patient organization. Tomeko brings these together on one hub.

Where can I find a specialist for Hereditary spastic paraplegia 36?

Use Tomeko's specialist and Centers-of-Excellence directories to find clinicians who treat Hereditary spastic paraplegia 36, filtered to your area.

Are there clinical trials for Hereditary spastic paraplegia 36?

Tomeko shows live, recruiting studies for Hereditary spastic paraplegia 36 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