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DOID:0060451 - Meesmann corneal dystrophy
Disease Ontology Definition:An epithelial and subepithelial dystrophy that is characterized by the formation of tiny round cysts in the corneal epithelium.
Synonyms: MECD, Stocker-Holt dystrophy, juvenile hereditary epithelial dystrophy
| OMIM:122100 - CORNEAL DYSTROPHY, MEESMANN, 1; MECD1 |
| MONDO:0007379 - Meesmann corneal dystrophy |
Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Xenbase Genes
:
krt12.5,
krt12.1,
krt12.6,
krt12.2,
krt12.4,
krt12.3
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD