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Disease Ontology Browser
Meesmann corneal dystrophy (DOID:0060451)
Alliance: disease page
Synonyms: juvenile hereditary epithelial dystrophy; MECD; Stocker-Holt dystrophy
Alt IDs: ICD10CM:H18.52, ICD9CM:371.51, MESH:D053559, NCI:C84795, OMIM:PS122100, ORDO:98954, UMLS_CUI:C0339277
Definition: An epithelial and subepithelial dystrophy that is characterized by the formation of tiny round cysts in the corneal epithelium.

Disease References using Mouse Models (1)
Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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Send questions and comments to User Support. 		last database update
10/29/2024
MGI 6.24 		The Jackson Laboratory