# Pierson syndrome

> Pierson syndrome is characterised by the association of congenital nephrotic syndrome and ocular anomalies with microcoria

**Wikidata**: [Q32136429](https://www.wikidata.org/wiki/Q32136429)  
**Source**: https://4ort.xyz/entity/pierson-syndrome


## References

1. Monarch Disease Ontology release 2018-06-29
2. Disease Ontology
3. UniProt
4. Human laminin beta2 deficiency causes congenital nephrosis with mesangial sclerosis and distinct eye abnormalities
5. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000172037/MONDO_0012184)
6. [Identifiers.org](https://registry.identifiers.org/registry/doid)