|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||Fibrosis of the external ocular muscles such that the eyes of affected individuals are partially or completely fixed in a strabismic position. Residual eye movements are significantly limited. (Human Phenotype Ontology, HP_0007936)|
|Downloads & Tools|
2 genes associated with the restrictive external ophthalmoplegia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.