Lattice corneal dystrophy type 1 [Supplementary Concept]
A hereditary autosomal dominant form of corneal dystrophy with significant phenotypic variability. It is characterized by polymorphic geographic deposits at BOWMAN'S MEMBRANE, lattice corneal dystrophy, recurrent corneal ulceration, and mild progressive visual impairment. Mutations in the TGFBI gene have been identified. OMIM: 122200
Date introduced: August 25, 2010
MeSH Unique ID: C537881
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Entry Terms:
- LCD1 Lattice Corneal Dystrophy 1
- Corneal dystrophy, lattice type 1
- Corneal Dystrophy, Lattice Type I
- Lattice Corneal Dystrophy, Type I
- Lattice Corneal Dystrophy Type I
- Biber-Haab-Dimmer Dystrophy
- CDL1 Corneal dystrophy, lattice type 1