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Oculocutaneous albinism type 1A

Just diagnosed with Oculocutaneous albinism type 1A?

You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Oculocutaneous albinism type 1A, look for clinical trials, and connect with others living with it — all in one place.

Open the full Oculocutaneous albinism type 1A hub →

Overview

Oculocutaneous albinism type 1A is a rare condition. Also known as OCA1A, Tyrosinase-negative oculocutaneous albinism. Tomeko brings together the specialists, research, clinical trials, treatments and community for Oculocutaneous albinism type 1A so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.

Identifiers: ORPHA:79431 · OMIM 203100 · ICD-10 E70.3 · GARD 0016721

Find care for Oculocutaneous albinism type 1A

Authoritative references for Oculocutaneous albinism type 1A

Common questions

I was just diagnosed with Oculocutaneous albinism type 1A — what should I do first?

Start by learning the basics from an authoritative source, find a specialist or center that sees Oculocutaneous albinism type 1A, and connect with a patient organization. Tomeko brings these together on one hub.

Where can I find a specialist for Oculocutaneous albinism type 1A?

Use Tomeko's specialist and Centers-of-Excellence directories to find clinicians who treat Oculocutaneous albinism type 1A, filtered to your area.

Are there clinical trials for Oculocutaneous albinism type 1A?

Tomeko shows live, recruiting studies for Oculocutaneous albinism type 1A 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