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.
Xenbase Genes : krt12.5, krt12.1, krt12.6, krt12.2, krt12.4, krt12.3
|OMIM:122100 - CORNEAL DYSTROPHY, MEESMANN, 1; MECD1|
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee