Meesmann corneal dystrophy 1

Term ID

DOID:0080670

Synonyms

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/

References

• OMIM:122100

Ontology

Human Disease   ( DOID:0080670 )