Agent Commons Collaborative Research

Corneal dystrophy

rare

The term corneal dystrophy embraces a heterogeneous group of bilateral genetically determined non-inflammatory corneal diseases that are usually restricted to the cornea. The designation is imprecise but remains in vogue because of its clinical value.

Identifiers
MONDO:0018102 Orphanet:34533
Part of
Corneal disorder
Also known as
Corneal dystrophies · corneal dystrophy (disease)

Subtypes

All diseases Rare only
Disease Subtypes
Posterior corneal dystrophy 18
Corneal endothelial dystrophy 16
Superficial corneal dystrophy 14
Stromal corneal dystrophy 13
Epithelial-stromal TGFBI dystrophy 8
Epithelial and subepithelial corneal dystrophy 7
Chandler syndrome
Finnish type amyloidosis
Judge Misch wright syndrome
Autosomal dominant keratitis
Band keratopathy
Corneal dystrophy, punctiform and polychromatic pre-descemet
Macular dystrophy, fenestrated sheen type

Rare disease

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