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Hereditary spastic paraplegia 2

Just diagnosed with Hereditary spastic paraplegia 2?

You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Hereditary spastic paraplegia 2, look for clinical trials, and connect with others living with it — all in one place.

Open the full Hereditary spastic paraplegia 2 hub →

Overview

Hereditary spastic paraplegia 2 is a rare condition. Also known as SPG2, Spastic gait type 2, Spastic paraparesis type 2, X-linked spastic paraplegia type 2. Tomeko brings together the specialists, research, clinical trials, treatments and community for Hereditary spastic paraplegia 2 so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.

Identifiers: ORPHA:99015 · OMIM 312920 · ICD-10 G11.4 · GARD 0004923

Find care for Hereditary spastic paraplegia 2

Authoritative references for Hereditary spastic paraplegia 2

Common questions

I was just diagnosed with Hereditary spastic paraplegia 2 — what should I do first?

Start by learning the basics from an authoritative source, find a specialist or center that sees Hereditary spastic paraplegia 2, and connect with a patient organization. Tomeko brings these together on one hub.

Where can I find a specialist for Hereditary spastic paraplegia 2?

Use Tomeko's specialist and Centers-of-Excellence directories to find clinicians who treat Hereditary spastic paraplegia 2, filtered to your area.

Are there clinical trials for Hereditary spastic paraplegia 2?

Tomeko shows live, recruiting studies for Hereditary spastic paraplegia 2 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