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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.


Parent Relationships

is_a Meesmann corneal dystrophy

is_a autosomal dominant disease

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