MeSH Browser

MeSH Supplementary: Lattice corneal dystrophy type 1
Unique ID: C537881
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C537881
Entry Term(s): 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
Registry Number: 0
Heading Mapped to: *Corneal Dystrophies, Hereditary
Frequency: 21
Note: 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 of Entry: 2010/08/25
Revision Date: 2019/06/24

Lattice corneal dystrophy type 1 MeSH Supplementary Concept Data 2023