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Feingold syndrome type 1

Just diagnosed with Feingold syndrome type 1?

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

Open the full Feingold syndrome type 1 hub →

Overview

Feingold syndrome type 1 is a rare condition. Also known as Brunner-Winter syndrome type 1, Digital anomalies with short palpebral fissures and atresia of esophagus or duodenum type 1, FGLDS1, FS1, MMT type 1, MODED syndrome type 1, Microcephaly-digital anomalies-normal intelligence syndrome type 1, Microcephaly-intellectual disability-tracheoesophageal fistula syndrome type 1. Tomeko brings together the specialists, research, clinical trials, treatments and community for Feingold syndrome type 1 so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.

Identifiers: ORPHA:391641 · OMIM 164280 · ICD-10 Q87.8 · GARD 0017624

Find care for Feingold syndrome type 1

Authoritative references for Feingold syndrome type 1

Common questions

I was just diagnosed with Feingold syndrome type 1 — what should I do first?

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

Where can I find a specialist for Feingold syndrome type 1?

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

Are there clinical trials for Feingold syndrome type 1?

Tomeko shows live, recruiting studies for Feingold syndrome type 1 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