|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||Abnormal development of the choroid and retina. (Human Phenotype Ontology, HP_0007731)|
|Downloads & Tools|
1 genes associated with the chorioretinal dysplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
|KIF11||kinesin family member 11|