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Oculotrichoanal syndrome

Just diagnosed with Oculotrichoanal syndrome?

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

Open the full Oculotrichoanal syndrome hub →

Overview

Oculotrichoanal syndrome is a rare condition. Also known as MOTA syndrome, Manitoba oculotrichoanal syndrome, Marles syndrome, Marles-Greenberg-Persaud syndrome. Tomeko brings together the specialists, research, clinical trials, treatments and community for Oculotrichoanal syndrome so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.

Identifiers: ORPHA:2717 · OMIM 248450 · ICD-10 Q87.8 · GARD 0003395

Find care for Oculotrichoanal syndrome

Authoritative references for Oculotrichoanal syndrome

Common questions

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

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

Where can I find a specialist for Oculotrichoanal syndrome?

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

Are there clinical trials for Oculotrichoanal syndrome?

Tomeko shows live, recruiting studies for Oculotrichoanal 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