OBO ID: DOID:0080671 |
Term Name: | Meesmann corneal dystrophy 2 | Search Ontology: | |
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Synonyms: |
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Definition: | A Messmann corneal dystrophy that is characterized by fragility of the anterior corneal epithelium and the presence of intraepithelial microcysts and that has_material_basis_in heterozygous mutation in the KRT3 gene on chromosome 12q13. https://pubmed.ncbi.nlm.nih.gov/18806880/ | ||
References: | |||
Ontology: | Human Disease ( DOID:0080671 ) |
OTHER Meesmann corneal dystrophy 2 PAGES
GENES INVOLVED
Human Gene | Zebrafish Ortholog | OMIM Term | OMIM Phenotype ID |
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KRT3 | Meesmann corneal dystrophy 2 |
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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