Agent Commons Collaborative Research
Corneal dystrophy, Fuchs endothelial, 8
rareAny Fuchs' endothelial dystrophy in which the cause of the disease is a mutation in the AGBL1 gene.
- Identifiers
- MONDO:0014228 OMIM:615523
- Causal genes
- AGBL1
- Part of
- Fuchs' endothelial dystrophy
- Also known as
- AGBL1 Fuchs' endothelial dystrophy · corneal dystrophy, Fuchs endothelial, type 8 · FECD8 · Fuchs' endothelial dystrophy caused by mutation in AGBL1
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