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RIDDLE syndrome

Just diagnosed with RIDDLE syndrome?

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

Open the full RIDDLE syndrome hub →

Overview

RIDDLE syndrome is a rare condition. Also known as RNF168 deficiency, Radiosensitivity-immunodeficiency-dysmorphic features-learning difficulties syndrome. Tomeko brings together the specialists, research, clinical trials, treatments and community for RIDDLE syndrome so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.

Identifiers: ORPHA:420741 · OMIM 611943 · ICD-10 D82.8 · GARD 0017701

Find care for RIDDLE syndrome

Authoritative references for RIDDLE syndrome

Common questions

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

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

Where can I find a specialist for RIDDLE syndrome?

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

Are there clinical trials for RIDDLE syndrome?

Tomeko shows live, recruiting studies for RIDDLE 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