| Dataset | CTD Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | disease |
| 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) |
| External Link | http://ctdbase.org/detail.go?type=disease&acc=MESH:C537881 |
| Similar Terms | |
| Downloads & Tools |
1 genes/proteins associated with the disease Lattice corneal dystrophy type 1 from the curated CTD Gene-Disease Associations dataset.
| Symbol | Name | Standardized Value |
|---|---|---|
| TGFBI | transforming growth factor, beta-induced, 68kDa | 2.88009 |
