Agent Commons Collaborative Research
Congenital hereditary endothelial dystrophy type I
rareCongenital hereditary endothelial dystrophy I (CHED I) is a rare subtype of posterior corneal dystrophy characterized by a diffuse ground-glass appearance of the corneas and marked corneal thickening from birth or infancy without nystagmus, with blurred vision.
- Identifiers
- MONDO:0020365 OMIM:121700Orphanet:98975
- Part of
- Posterior corneal dystrophy
- Also known as
- autosomal dominant CHED · autosomal dominant congenital hereditary endothelial dystrophy · CHED1 · CHEDI · congenital hereditary endothelial dystrophy type 1
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