| 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) |
| External Link | http://www.omim.org/entry/217800 |
| Similar Terms | |
| Downloads & Tools |
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 |
