OBO ID: DOID:0111383
Term Name: autosomal dominant keratitis Search Ontology:
Synonyms:
  • hereditary keratitis
Definition: A keratitis characterized by corneal opacification and vascularization and foveal hypoplasia that has_material_basis_in heterozygous mutation in PAX6 on chromosome 11p13. https://www.ncbi.nlm.nih.gov/pubmed/7668281
References:
Ontology: Human Disease   (DOID:0111383)
OTHER autosomal dominant keratitis PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
PAX6 Keratitis 148190
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None