| Dataset | HPO Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | Slender, slit-like aperture of the nostril. (Human Phenotype Ontology, HP_0009933) |
| External Link | http://compbio.charite.de/hpoweb/showterm?id=HP:0009933 |
| Similar Terms | |
| Downloads & Tools |
1 genes associated with the narrow naris phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| ESCO2 | establishment of sister chromatid cohesion N-acetyltransferase 2 |
