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Human Disease
Meesmann corneal dystrophy 1
- Term ID
- DOID:0080670
- Synonyms
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- 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 )
- is a type of
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Genes Involved
Zebrafish Models