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Dyskeratosis congenita

Just diagnosed with Dyskeratosis congenita?

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

Open the full Dyskeratosis congenita hub →

Overview

Dyskeratosis congenita is a rare condition. Also known as DC, DKC, Zinsser-Engman-Cole syndrome. Tomeko brings together the specialists, research, clinical trials, treatments and community for Dyskeratosis congenita so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.

Identifiers: ORPHA:1775 · OMIM 127550, 224230, 305000 · ICD-10 Q82.8 · GARD 0010905

Find care for Dyskeratosis congenita

Authoritative references for Dyskeratosis congenita

Common questions

I was just diagnosed with Dyskeratosis congenita — what should I do first?

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

Where can I find a specialist for Dyskeratosis congenita?

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

Are there clinical trials for Dyskeratosis congenita?

Tomeko shows live, recruiting studies for Dyskeratosis congenita 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