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Glomuvenous malformation

Just diagnosed with Glomuvenous malformation?

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

Open the full Glomuvenous malformation hub →

Overview

Glomuvenous malformation is a rare condition. Also known as Glomangiomatosis, Hereditary multiple glomangiomas, Multiple glomus tumors, VMGLOM, Venous malformations with glomus cells. Tomeko brings together the specialists, research, clinical trials, treatments and community for Glomuvenous malformation so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.

Identifiers: ORPHA:83454 · OMIM 138000 · ICD-10 Q27.8 · GARD 0016728

Find care for Glomuvenous malformation

Authoritative references for Glomuvenous malformation

Common questions

I was just diagnosed with Glomuvenous malformation — what should I do first?

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

Where can I find a specialist for Glomuvenous malformation?

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

Are there clinical trials for Glomuvenous malformation?

Tomeko shows live, recruiting studies for Glomuvenous malformation 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