|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||Congenital non-progressive ophthalmoplegia with multiple extraocular muscle restrictions. Typically, there is ptosis and variable degrees of restriction of horizontal and vertical eye movements. (Human Phenotype Ontology, HP_0001491)|
|Downloads & Tools|
4 genes associated with the congenital fibrosis of extraocular muscles phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.