# helicoid peripapillary chorioretinal degeneration

> eye disease characterized by presence in the fundus of progressive bilateral retinal and choroidal atrophy leading to central vision loss that has material basis in heterozygous muation in TEAD1 on 11p15.3

**Wikidata**: [Q55780357](https://www.wikidata.org/wiki/Q55780357)  
**Source**: https://4ort.xyz/entity/helicoid-peripapillary-chorioretinal-degeneration


## References

1. Monarch Disease Ontology release 2018-06-29
2. Disease Ontology
3. Mapping the locus of atrophia areata, a helicoid peripapillary chorioretinal degeneration with autosomal dominant inheritance, to chromosome 11p15
4. [Identifiers.org](https://registry.identifiers.org/registry/doid)