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Leber congenital amaurosis

Just diagnosed with Leber congenital amaurosis?

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

Open the full Leber congenital amaurosis hub →

Overview

Leber congenital amaurosis is a rare condition. Also known as Amaurosis congenita of Leber. Tomeko brings together the specialists, research, clinical trials, treatments and community for Leber congenital amaurosis so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.

Identifiers: ORPHA:65 · OMIM 179900, 204000, 204100 · ICD-10 H35.5 · GARD 0000634

Find care for Leber congenital amaurosis

Authoritative references for Leber congenital amaurosis

Common questions

I was just diagnosed with Leber congenital amaurosis — what should I do first?

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

Where can I find a specialist for Leber congenital amaurosis?

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

Are there clinical trials for Leber congenital amaurosis?

Tomeko shows live, recruiting studies for Leber congenital amaurosis 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