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CCDC115-CDG

Just diagnosed with CCDC115-CDG?

You are not alone. Here is where to start: learn the basics, find a specialist or center that sees CCDC115-CDG, look for clinical trials, and connect with others living with it — all in one place.

Open the full CCDC115-CDG hub →

Overview

CCDC115-CDG is a rare condition. Also known as CDG syndrome type IIo, CDG-IIo, CDG2O, Carbohydrate deficient glycoprotein syndrome type IIo, Congenital disorder of glycosylation type 2o, Congenital disorder of glycosylation type IIo. Tomeko brings together the specialists, research, clinical trials, treatments and community for CCDC115-CDG so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.

Identifiers: ORPHA:468684 · OMIM 616828 · ICD-10 E77.8 · GARD 0017845

Find care for CCDC115-CDG

Authoritative references for CCDC115-CDG

Common questions

I was just diagnosed with CCDC115-CDG — what should I do first?

Start by learning the basics from an authoritative source, find a specialist or center that sees CCDC115-CDG, and connect with a patient organization. Tomeko brings these together on one hub.

Where can I find a specialist for CCDC115-CDG?

Use Tomeko's specialist and Centers-of-Excellence directories to find clinicians who treat CCDC115-CDG, filtered to your area.

Are there clinical trials for CCDC115-CDG?

Tomeko shows live, recruiting studies for CCDC115-CDG 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