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Scleromyxedema

Just diagnosed with Scleromyxedema?

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

Open the full Scleromyxedema hub →

Overview

Scleromyxedema is a rare condition. Also known as Arndt-Gottron disease, Generalized lichenoid papular eruption, Generalized papular and sclerodermoid lichen myxedematosus. Tomeko brings together the specialists, research, clinical trials, treatments and community for Scleromyxedema so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.

Identifiers: ORPHA:167635 · ICD-10 L98.5 · GARD 0007615

Find care for Scleromyxedema

Authoritative references for Scleromyxedema

Common questions

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

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

Where can I find a specialist for Scleromyxedema?

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

Are there clinical trials for Scleromyxedema?

Tomeko shows live, recruiting studies for Scleromyxedema 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