|Dataset||CTD Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||An eye disease characterized by missing pieces of tissue in structures that form the eye, such as the iris, retina, choroid or optic disc. (Human Disease Ontology, DOID_12270)|
|Downloads & Tools|
7 genes/proteins associated with the disease Coloboma from the curated CTD Gene-Disease Associations dataset.