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Inclusion body myositis

Just diagnosed with Inclusion body myositis?

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

Open the full Inclusion body myositis hub →

Overview

Inclusion body myositis is a rare condition. Also known as IBM, Sporadic inclusion body myositis, sIBM. Tomeko brings together the specialists, research, clinical trials, treatments and community for Inclusion body myositis so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.

Identifiers: ORPHA:611 · OMIM 147421 · ICD-10 M60.8 · GARD 0003896

Find care for Inclusion body myositis

Authoritative references for Inclusion body myositis

Common questions

I was just diagnosed with Inclusion body myositis — what should I do first?

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

Where can I find a specialist for Inclusion body myositis?

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

Are there clinical trials for Inclusion body myositis?

Tomeko shows live, recruiting studies for Inclusion body myositis 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