Search Ontology:
Human Disease

autosomal dominant keratitis

Term ID
DOID:0111383
Synonyms
  • hereditary keratitis
Definition
A keratitis characterized by corneal opacification and vascularization and foveal hypoplasia that has_material_basis_in heterozygous mutation in the PAX6 gene on chromosome 11p13. https://www.ncbi.nlm.nih.gov/pubmed/7668281
References
Ontology
Human Disease   ( DOID:0111383 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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