corneal dystrophy, groenouw type i Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
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)
External Link http://www.omim.org/entry/121900
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Genes

1 genes associated with the corneal dystrophy, groenouw type i phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
TGFBI transforming growth factor, beta-induced, 68kDa