| Dataset | OMIM Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | Meesmann corneal dystrophy (MECD) is a rare form of superficial corneal dystrophy characterized by distinct tiny bubble-like, round-to-oval punctate bilateral opacities in the central corneal epithelium, and to a lesser extent in the peripheral cornea, with little impact on vision. (Orphanet Rare Disease Ontology, Orphanet_98954) |
| External Link | http://www.omim.org/entry/122100 |
| Similar Terms | |
| Downloads & Tools |
2 genes associated with the meesmann corneal dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
