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Familial dysautonomia

Just diagnosed with Familial dysautonomia?

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

Open the full Familial dysautonomia hub →

Overview

Familial dysautonomia is a rare condition. Also known as HSAN3, Hereditary sensory and autonomic neuropathy type 3, Hereditary sensory and autonomic neuropathy type III, Riley-Day syndrome. Tomeko brings together the specialists, research, clinical trials, treatments and community for Familial dysautonomia so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.

Identifiers: ORPHA:1764 · OMIM 223900 · ICD-10 G90.1 · GARD 0007581

Find care for Familial dysautonomia

Authoritative references for Familial dysautonomia

Common questions

I was just diagnosed with Familial dysautonomia — what should I do first?

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

Where can I find a specialist for Familial dysautonomia?

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

Are there clinical trials for Familial dysautonomia?

Tomeko shows live, recruiting studies for Familial dysautonomia 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