autosomal dominant keratitis
MeSH: C537022ORPHA: 2334
Overview
Hereditary keratitis is characterised by opacification and vascularisation of the cornea, often associated with macula hypoplasia
Available Treatments (0)
No treatments linked yet
Clinical trials or compassionate use may be available — consult a specialist.
Clinical Presentation
Signs and symptoms associated with autosomal dominant keratitis, sourced from HPO and Orphanet clinical annotations.
KeratitisAbnormality of refractionMacular hypoplasiaReduced visual acuityHypoplasia of the foveaOpacification of the corneal stromaHypoplastic iris stromaCorneal neovascularizationAbnormal corneal limbus morphologyLimbal stem cell deficiencyMicrocorneaCataractAniridiaColobomaCongenital nystagmusBilateral microphthalmos
Classification & Codes
MeSH Code
C537022Orphanet Code
ORPHA:2334autosomal dominant keratitis
| MeSH | C537022 |
| Orphanet | ORPHA:2334 |
| Treatments | 0 drug(s) |
| Symptoms on record | 16 signs |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO