helicoid peripapillary chorioretinal degeneration
MeSH: C566236ORPHA: 86813
Overview
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
Available Treatments (0)
No treatments linked yet
Clinical trials or compassionate use may be available — consult a specialist.
Classification & Codes
MeSH Code
C566236Orphanet Code
ORPHA:86813helicoid peripapillary chorioretinal degeneration
| MeSH | C566236 |
| Orphanet | ORPHA:86813 |
| Treatments | 0 drug(s) |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO