Macular Corneal Dystrophy Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A corneal dystrophy that is characterized by corneal haze, bilateral loss of vision, eventually necessitating corneal transplantation resulting from progressive punctate opacities in the cornea. (Human Disease Ontology, DOID_2565)
External Link https://www.disgenet.org/browser/0/1/0/C0024439
Similar Terms
Downloads & Tools

Genes

5 genes associated with the disease Macular Corneal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
CHST6 carbohydrate (N-acetylglucosamine 6-O) sulfotransferase 6
LCAT lecithin-cholesterol acyltransferase
TAT tyrosine aminotransferase
TGFBI transforming growth factor, beta-induced, 68kDa
VSX1 visual system homeobox 1