Meesmann corneal dystrophy 1

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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:

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: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

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