meesmann corneal dystrophy Gene Set

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
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Genes

2 genes associated with the meesmann corneal dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
KRT12 keratin 12, type I
KRT3 keratin 3, type II