Lattice Corneal Dystrophy

About the Disease
Lattice Corneal Dystrophy, also known as familial amyloid neuropathy, finnish type, is related to corneal dystrophy, lattice type i and corneal dystrophy, gelatinous drop-like. An important gene associated with Lattice Corneal Dystrophy is TGFBI (Transforming Growth Factor Beta Induced), and among its related pathways/superpathways are "Ca, cAMP and Lipid Signaling" and Coregulation of Androgen receptor activity. Affiliated tissues include cornea, eye and kidney, and related phenotypes are no effect and no effect

Common Targets
GSN | TACSTD2 | G3576 | TGFBI

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