|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|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.
|SLC9A6||solute carrier family 9, subfamily A (NHE6, cation proton antiporter 6), member 6|