| Dataset | HPO Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | A fixed reduction in the vertical distance between the upper and lower eyelids with short palpebral fissures on one side only. (Human Phenotype Ontology, HP_0007946) |
| External Link | http://compbio.charite.de/hpoweb/showterm?id=HP:0007946 |
| Similar Terms | |
| Downloads & Tools |
1 genes associated with the unilateral narrow palpebral fissure phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| SMARCA2 | SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 2 |
