OBO ID: DOID:0080670 |
Term Name: | Meesmann corneal dystrophy 1 | Search Ontology: | |
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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 ) |
OTHER Meesmann corneal dystrophy 1 PAGES
GENES INVOLVED
Human Gene | Zebrafish Ortholog | OMIM Term | OMIM Phenotype ID |
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KRT12 | Meesmann corneal dystrophy 1 |
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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