|Dataset||CTD Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||Type I lattice corneal dystrophy (LCDI) is a frequent form of stromal corneal dystrophy (see this term) characterized by a network of delicate interdigitating branching filamentous opacities within the cornea with progressive visual impairment and no systemic manifestations. (Orphanet Rare Disease Ontology, Orphanet_98964)|
|Downloads & Tools|
1 genes/proteins associated with the disease Lattice corneal dystrophy type 1 from the curated CTD Gene-Disease Associations dataset.
|TGFBI||transforming growth factor, beta-induced, 68kDa||2.88009|