# exudative vitreoretinopathy

> retinal vascular disease characterized by the prevention of blood vessel formation at the edges of the retina and the hemorrhage of the blood vessels in the retina

**Wikidata**: [Q5432936](https://www.wikidata.org/wiki/Q5432936)  
**Wikipedia**: [English](https://en.wikipedia.org/wiki/Familial_exudative_vitreoretinopathy)  
**Source**: https://4ort.xyz/entity/exudative-vitreoretinopathy


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. Next-generation sequencing of a 40 Mb linkage interval reveals TSPAN12 mutations in patients with familial exudative vitreoretinopathy
4. A mutation in the Norrie disease gene (NDP) associated with X-linked familial exudative vitreoretinopathy
5. Mutations in LRP5 or FZD4 underlie the common familial exudative vitreoretinopathy locus on chromosome 11q.
6. ZNF408 is mutated in familial exudative vitreoretinopathy and is crucial for the development of zebrafish retinal vasculature
7. [Identifiers.org](https://registry.identifiers.org/registry/doid)