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Metadata
ID	DOID:0080671
Name	Meesmann corneal dystrophy 2
Definition	A Messmann corneal dystrophy that is characterized by fragility of the anterior corneal epithelium and the presence of intraepithelial microcysts and that has_material_basis_in heterozygous mutation in the KRT3 gene on chromosome 12q13. https://pubmed.ncbi.nlm.nih.gov/18806880/
Xrefs	MIM:618767
Parent Relationships	is_a autosomal dominant disease is_a Meesmann corneal dystrophy
Subclass Logical Relationships	has material basis in some autosomal dominant inheritance