tomeko

CEBALID syndrome

Just diagnosed with CEBALID syndrome?

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

Open the full CEBALID syndrome hub →

Overview

CEBALID syndrome is a rare condition. Also known as CEBALID, Craniofacial defects-dysmorphic ears-brain abnormalities-language delay-intellectual disability, MCTT, MN1 C-terminal truncation syndrome. Tomeko brings together the specialists, research, clinical trials, treatments and community for CEBALID syndrome so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.

Identifiers: ORPHA:693549 · OMIM 618774 · GARD 0027949

Find care for CEBALID syndrome

Authoritative references for CEBALID syndrome

Common questions

I was just diagnosed with CEBALID syndrome — what should I do first?

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

Where can I find a specialist for CEBALID syndrome?

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

Are there clinical trials for CEBALID syndrome?

Tomeko shows live, recruiting studies for CEBALID syndrome 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