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Human Disease and Mouse Model Detail
Human Disease Corneal Dystrophy, Fuchs Endothelial, 2; FECD2
OMIM ID: 610158
Synonyms Corneal Dystrophy, Fuchs Endothelial; Corneal Dystrophy, Fuchs Endothelial, Late-Onset; Fcd1 Locus
Genes and
mouse models
There are currently no human or mouse genes associated with this disease in the MGI database.

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
MGI 6.03
The Jackson Laboratory