Disease #01402 (keratitis, hereditary, OMIM:148190)

Official abbreviation -
Name keratitis, hereditary
OMIM ID 148190
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene PAX6
Associated tissues -
Disease features -
Remarks -