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Neuroferritinopathy

Just diagnosed with Neuroferritinopathy?

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

Open the full Neuroferritinopathy hub →

Overview

Neuroferritinopathy is a rare condition. Also known as Adult basal ganglia disease, Ferritin-related neurodegeneration, Hereditary ferritinopathy. Tomeko brings together the specialists, research, clinical trials, treatments and community for Neuroferritinopathy so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.

Identifiers: ORPHA:157846 · OMIM 606159 · ICD-10 G23.0 · GARD 0010686

Find care for Neuroferritinopathy

Authoritative references for Neuroferritinopathy

Common questions

I was just diagnosed with Neuroferritinopathy — what should I do first?

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

Where can I find a specialist for Neuroferritinopathy?

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

Are there clinical trials for Neuroferritinopathy?

Tomeko shows live, recruiting studies for Neuroferritinopathy 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