Lattice Corneal Dystrophy

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 eye and kidney, and related phenotypes are Increased SMN2 exon 7 inclusion and homeostasis/metabolism