Visualize Submit Comment

Metadata
ID	DOID:0080670
Name	Meesmann corneal dystrophy 1
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. https://pubmed.ncbi.nlm.nih.gov/22174841/
Xrefs	OMIM:122100
Parent Relationships	is_a Meesmann corneal dystrophy is_a autosomal dominant disease