| Dataset | HPO Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| External Link | http://compbio.charite.de/hpoweb/showterm?id=HP:0006794 |
| Similar Terms | |
| Downloads & Tools |
1 genes associated with the loss of ability to walk in first decade phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| SLC9A6 | solute carrier family 9, subfamily A (NHE6, cation proton antiporter 6), member 6 |
