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Corneal dystrophy, Fuchs' endothelial, 1 MeSH Supplementary Concept Data 2022


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 Number
0
Heading Mapped to
*Fuchs' Endothelial Dystrophy
Frequency
21
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 Preferred
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