macular corneal dystrophy Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
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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1 genes associated with the macular corneal dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
CHST6 carbohydrate (N-acetylglucosamine 6-O) sulfotransferase 6