OBO ID: DOID:0080670
Term Name: Meesmann corneal dystrophy 1 Search Ontology:
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 )
OTHER Meesmann corneal dystrophy 1 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
KRT12 Meesmann corneal dystrophy 1
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None