# Wagner's disease

> Wagner disease is a rare hereditary vitreoretinopathy characterized by an anomaleous vitreous associated with myopia, cataract, chorioretinal atrophy, and peripheral tractional or rhegmatogenous retinal detachment

**Wikidata**: [Q2470609](https://www.wikidata.org/wiki/Q2470609)  
**Wikipedia**: [English](https://en.wikipedia.org/wiki/Wagner's_disease)  
**Source**: https://4ort.xyz/entity/wagner-s-disease


## References

1. Monarch Disease Ontology release 2018-06-29
2. Human Phenotype Ontology release 2018-03-08
3. UniProt
4. Identification of a novel splice site mutation of the CSPG2 gene in a Japanese family with Wagner syndrome
5. [ClinGen](https://search.clinicalgenome.org/kb/gene-validity/CGGV:assertion_d1ea2623-463f-40f1-befb-5dfde7abc784-2021-07-26T183919.943Z)
6. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000038427/MONDO_0007740)