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Autosomal recessive bestrophinopathy

Just diagnosed with Autosomal recessive bestrophinopathy?

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

Open the full Autosomal recessive bestrophinopathy hub →

Overview

Autosomal recessive bestrophinopathy is a rare condition. Also known as Retinopathy, Burgess-Black type. Tomeko brings together the specialists, research, clinical trials, treatments and community for Autosomal recessive bestrophinopathy so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.

Identifiers: ORPHA:139455 · OMIM 611809 · ICD-10 H35.5 · GARD 0010301

Find care for Autosomal recessive bestrophinopathy

Authoritative references for Autosomal recessive bestrophinopathy

Common questions

I was just diagnosed with Autosomal recessive bestrophinopathy — what should I do first?

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

Where can I find a specialist for Autosomal recessive bestrophinopathy?

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

Are there clinical trials for Autosomal recessive bestrophinopathy?

Tomeko shows live, recruiting studies for Autosomal recessive bestrophinopathy 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