macular corneal dystrophy Gene Set

Dataset DISEASES Text-mining Gene-Disease Assocation Evidence Scores
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)
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Genes

16 genes co-occuring with the disease macular corneal dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
CHST6 carbohydrate (N-acetylglucosamine 6-O) sulfotransferase 6 3.71807
GLYCAM1 glycosylation dependent cell adhesion molecule 1 (pseudogene) 1.55779
CHST1 carbohydrate (keratan sulfate Gal-6) sulfotransferase 1 1.54318
CHST5 carbohydrate (N-acetylglucosamine 6-O) sulfotransferase 5 1.45748
TGFBI transforming growth factor, beta-induced, 68kDa 1.40045
LUM lumican 0.984321
KRT12 keratin 12, type I 0.96918
COL8A2 collagen, type VIII, alpha 2 0.929587
KRT3 keratin 3, type II 0.84585
GSN gelsolin 0.804026
VSX1 visual system homeobox 1 0.801154
LCAT lecithin-cholesterol acyltransferase 0.777386
IDS iduronate 2-sulfatase 0.536957
GLB1 galactosidase, beta 1 0.50689
DCN decorin 0.401572
GGT2 gamma-glutamyltransferase 2 0.258064