Disease #04337 (FECD (dystrophy, corneal, Fuchs endothelial (FECD)))
Official abbreviation |
FECD |
Name |
dystrophy, corneal, Fuchs endothelial (FECD) |
OMIM ID |
- |
Inheritance |
- |
Individuals reported having this disease |
8 |
Phenotype entries for this disease |
8 |
Associated with 0 genes |
- |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Individuals
|
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