MeSH Browser

MeSH Supplementary: Corneal dystrophy, Fuchs' endothelial, 1
Unique ID: C535478
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C535478
Entry Term(s): Corneal Dystrophy, Fuchs Endothelial, 1; Corneal Dystrophy, Fuchs Endothelial, Early-Onset; Corneal dystrophy, Fuchs' endothelial, early-onset; Dystrophia epithelialis corneae; Early-onset FECD Early-onset Fuchs' endothelial corneal dystrophy; FECD1 Fuchs' endothelial corneal dystrophy 1; Fuchs' dystrophy; Fuchs' endothelial corneal dystrophy, early-onset
Registry Numbers: 0
Heading Mapped to: *Fuchs' Endothelial Dystrophy
Frequency: 32
Note: Hereditary Fuch's Endothelial Corneal Dystrophy that is caused by mutations in the COLLAGEN TYPE VIII alpha-2 gene (COL8A2). OMIM: 136800
Date of Entry: 2010/08/25
Revision Date: 2019/06/24

Corneal dystrophy, Fuchs' endothelial, 1 MeSH Supplementary Concept Data 2025