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Crigler-Najjar syndrome

Specialists and centers, recruiting clinical trials, patient organizations, research, and community for Crigler-Najjar syndrome — brought together in one place.

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Just diagnosed with Crigler-Najjar syndrome?

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

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Overview

Crigler-Najjar syndrome is a rare condition. Also known as Bilirubin uridinediphosphate glucuronosyltransferase deficiency, Bilirubin-UGT deficiency. Tomeko brings together the specialists, research, clinical trials, treatments and community for Crigler-Najjar syndrome so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.

Identifiers: ORPHA:205 · OMIM 218800, 606785 · ICD-10 E80.5 · GARD 0016526

Find care for Crigler-Najjar syndrome

Authoritative references for Crigler-Najjar syndrome

Research & market landscape for Crigler-Najjar syndrome

Following Crigler-Najjar syndrome for research or industry? Tomeko brings together the recruiting trials, the latest literature, patient organizations, and the specialist and care-center footprint for Crigler-Najjar syndrome — the real-world landscape behind the condition, in one place.

Researchers, patient organizations & industry: Tomeko provides de-identified, no-PHI demand and engagement signal, trial awareness, and a labeled, editorially-firewalled presence for Crigler-Najjar syndrome and every rare condition. See how Tomeko works with industry →

Common questions

What is Crigler-Najjar syndrome?

Crigler-Najjar syndrome is a rare condition. Also known as Bilirubin uridinediphosphate glucuronosyltransferase deficiency, Bilirubin-UGT deficiency. For an authoritative medical description see the reference sources on this page; Tomeko brings the specialists, clinical trials, patient organizations and community for Crigler-Najjar syndrome together in one place.

What are the symptoms of Crigler-Najjar syndrome?

Symptoms of Crigler-Najjar syndrome vary from person to person. For a reviewed, plain-language overview see the authoritative references below (NIH GARD, Orphanet), and discuss your own symptoms with a clinician who treats Crigler-Najjar syndrome.

How is Crigler-Najjar syndrome treated?

Treatment for Crigler-Najjar syndrome depends on the individual and is managed by specialists. Use Tomeko to find clinicians and Centers of Excellence who see Crigler-Najjar syndrome, and review current options with them.

What causes Crigler-Najjar syndrome — is it genetic?

The cause and inheritance of Crigler-Najjar syndrome are described in the authoritative references linked on this page. A genetics or specialist clinician who treats Crigler-Najjar syndrome can explain what it means for you and your family.

I was just diagnosed with Crigler-Najjar syndrome — what should I do first?

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

Where can I find a specialist for Crigler-Najjar syndrome?

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

Are there clinical trials for Crigler-Najjar syndrome?

Tomeko shows live, recruiting studies for Crigler-Najjar syndrome from ClinicalTrials.gov on the hub.

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