Wagner's disease
ICD-10: H35.5MeSH: C536075ORPHA: 247834
Overview
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
Available Treatments (0)
No treatments linked yet
Clinical trials or compassionate use may be available — consult a specialist.
Classification & Codes
ICD-10 Code
H35.5MeSH Code
C536075Orphanet Code
ORPHA:247834Wagner's disease
| ICD-10 | H35.5 |
| MeSH | C536075 |
| Orphanet | ORPHA:247834 |
| Treatments | 0 drug(s) |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO