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Start free with EleplanIsolated congenital sclerocornea
ORPHA:91490Morphological anomaly
What it is
A rare corneal disorder characterized by non-inflammatory, non-progressive, bilateral ingrowth of vascularized, opaque scleral tissue into the peripheral cornea, obliterating the corneoscleral limbus and scleral sulcus. The condition is not associated with other ocular abnormalities.
Key facts
- Inheritance
- Autosomal dominant
- Classified as
- Morphological anomaly
Gene
ICD-10 codes
Cross-references
Orphadata Science: Free access data from Orphanet. © INSERM 1999. Data version 2026-06-23. Available under CC BY 4.0. This is a reference, not medical advice.
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