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Familial expansile osteolysis

Just diagnosed with Familial expansile osteolysis?

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

Open the full Familial expansile osteolysis hub →

Overview

Familial expansile osteolysis is a rare condition. Also known as Hereditary expansile polyostotic osteolytic dysplasia, McCabe disease. Tomeko brings together the specialists, research, clinical trials, treatments and community for Familial expansile osteolysis so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.

Identifiers: ORPHA:85195 · OMIM 174810 · ICD-10 M89.5 · GARD 0009168

Find care for Familial expansile osteolysis

Authoritative references for Familial expansile osteolysis

Common questions

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

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

Where can I find a specialist for Familial expansile osteolysis?

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

Are there clinical trials for Familial expansile osteolysis?

Tomeko shows live, recruiting studies for Familial expansile osteolysis 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