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DO Term : Meesmann corneal dystrophy 1 [DOID:0080670] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  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:
  • OMIM:122100,
  • 122100
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