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Summary Literature (0)
DOID:0080670 - Meesmann corneal dystrophy 1


Disease Ontology Definition:A Messmann corneal dystrophy that is characterized by the presence of multitudinous microcysts within the anterior epithelium and that has_material_basis_in heterozygous mutation in the KRT12 gene on chromosome 17q21.

Synonyms:

Referenced OMIM:
OMIM:122100 - CORNEAL DYSTROPHY, MEESMANN; MECD

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): Meesmann corneal dystrophy (is_a), autosomal dominant disease (is_a)


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