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CANOMAD syndrome

Just diagnosed with CANOMAD syndrome?

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

Open the full CANOMAD syndrome hub →

Overview

CANOMAD syndrome is a rare condition. Also known as CANDA syndrome, Chronic ataxic neuropathy-ophthalmoplegia-IgM paraprotein-cold agglutinins-disialosyl antibodies syndrome, Chronic sensory ataxic neuropathy with anti-disialosyl IgM antibodies. Tomeko brings together the specialists, research, clinical trials, treatments and community for CANOMAD syndrome so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.

Identifiers: ORPHA:71279 · ICD-10 G61.8 · GARD 0009778

Find care for CANOMAD syndrome

Authoritative references for CANOMAD syndrome

Common questions

I was just diagnosed with CANOMAD syndrome — what should I do first?

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

Where can I find a specialist for CANOMAD syndrome?

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

Are there clinical trials for CANOMAD syndrome?

Tomeko shows live, recruiting studies for CANOMAD syndrome 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