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Summary Literature (0)
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

In OMIM:
OMIM:122100 - CORNEAL DYSTROPHY, MEESMANN, 1; MECD1

In Mondo Disease Ontology:
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
Parent(s): epithelial and subepithelial dystrophy (is_a)