|Dataset||OMIM Gene-Disease Associations|
|Category||disease or phenotype associations|
|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)|
|Downloads & Tools|
2 genes associated with the meesmann corneal dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.