| Dataset | HPO Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | Duane anomaly is a congenital eye movement impairment with limitation of the ability to adduct or abduct the eye. When affected eyes are adducted (moved inwards towards the nose), the eyeball retracts and the palpebral fissure narrows. (Human Phenotype Ontology, HP_0009921) |
| External Link | http://compbio.charite.de/hpoweb/showterm?id=HP:0009921 |
| Similar Terms | |
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6 genes associated with the duane anomaly phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
