Meesmann corneal dystrophy

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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

Referenced OMIM:

OMIM:122100 - CORNEAL DYSTROPHY, MEESMANN; MECD

OMIM:122100 - CORNEAL DYSTROPHY, MEESMANN; MECD

Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: 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)

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Version: 4.15.0

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