# Wolcott-Rallison syndrome

> Wolcott-Rallison syndrome (WRS) is a very rare genetic disease, characterized by permanent neonatal diabetes mellitus (PNDM) with multiple epiphyseal dysplasia and other clinical manifestations, including recurrent episodes of acute liver failure

**Wikidata**: [Q8029730](https://www.wikidata.org/wiki/Q8029730)  
**Wikipedia**: [English](https://en.wikipedia.org/wiki/Wolcott–Rallison_syndrome)  
**Source**: https://4ort.xyz/entity/wolcott-rallison-syndrome


## References

1. Monarch Disease Ontology release 2018-06-29
2. Disease Ontology
3. UniProt
4. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000172071/MONDO_0009192)
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)