|Dataset||OMIM Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||Type I granular corneal dystrophy (GCDI) is a rare form of stromal corneal dystrophy (see this term) characterized by multiple small deposits in the superficial central corneal stroma, and progressive visual impairment, which may sometimes be severe. (Orphanet Rare Disease Ontology, Orphanet_98962)|
|Downloads & Tools|
1 genes associated with the corneal dystrophy, groenouw type i phenotype from the curated OMIM Gene-Disease Associations dataset.
|TGFBI||transforming growth factor, beta-induced, 68kDa|