Corneal Dystrophy, Juvenile Epithelial of Meesmann
An autosomal dominant form of hereditary corneal dystrophy due to a defect in cornea-specific KERATIN formation. Mutations in the genes that encode KERATIN-3 and KERATIN-12 have been linked to this disorder.
Year introduced: 2007
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Subheadings:
Tree Number(s): C11.204.236.218, C11.270.162.218, C16.320.290.162.204
MeSH Unique ID: D053559
Entry Terms:
- Corneal Dystrophy, Meesmann Epithelial
- Meesmann Corneal Dystrophy
- Corneal Dystrophy, Meesmann
- Corneal Dystrophies, Meesmann
- Dystrophies, Meesmann Corneal
- Meesmann Corneal Dystrophies
- Meesmann Epithelial Corneal Dystrophy
- Juvenile Hereditary Epithelial Dystrophy
- Meesmann Corneal Epithelial Dystrophy
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