# PCWH syndrome

> human disease

**Wikidata**: [Q30989286](https://www.wikidata.org/wiki/Q30989286)  
**Source**: https://4ort.xyz/entity/pcwh-syndrome


## References

1. Monarch Disease Ontology release 2018-06-29
2. Disease Ontology
3. UniProt
4. Neurological phenotype in Waardenburg syndrome type 4 correlates with novel SOX10 truncating mutations and expression in developing brain
5. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000100146/MONDO_0012198)
6. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000100146/Orphanet_163746)
7. [Identifiers.org](https://registry.identifiers.org/registry/doid)