# Dubin-Johnson syndrome

> rare, autosomal recessive, benign disorder that causes an isolated increase of conjugated bilirubin in the serum

**Wikidata**: [Q1263039](https://www.wikidata.org/wiki/Q1263039)  
**Wikipedia**: [English](https://en.wikipedia.org/wiki/Dubin–Johnson_syndrome)  
**Source**: https://4ort.xyz/entity/dubin-johnson-syndrome


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. Freebase Data Dumps. 2013
4. [Source](http://www.patient.co.uk/patientplus/d.htm)
5. UniProt
6. Mutations in the canilicular multispecific organic anion transporter (cMOAT) gene, a novel ABC transporter, in patients with hyperbilirubinemia II/Dubin-Johnson syndrome
7. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000023839/MONDO_0009380)
8. [Identifiers.org](https://registry.identifiers.org/registry/doid)