OBO ID: DOID:0080671
Term Name: Meesmann corneal dystrophy 2 Search Ontology:
Synonyms:
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
KRT3 Meesmann corneal dystrophy 2
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None