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
Also Known As:
Biber-Haab-Dimmer Dystrophy; CDL1 Corneal dystrophy, lattice type 1; Corneal Dystrophy, Lattice Type I; Corneal dystrophy, lattice type 1; LCD1 Lattice Corneal Dystrophy 1; Lattice Corneal Dystrophy Type I; Lattice Corneal Dystrophy, Type I