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Human Disease

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
Ontology
Human Disease   ( DOID:0080670 )
Relationships
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Genes Involved
Zebrafish Models