|Dataset||OMIM Gene-Disease Associations|
|Category||disease or phenotype associations|
|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)|
|Downloads & Tools|
1 genes associated with the macular corneal dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
|CHST6||carbohydrate (N-acetylglucosamine 6-O) sulfotransferase 6|