| Dataset | HPO Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | A bone structure disease that has_material_basis_in displacement located_in set of vertebrae. (Human Disease Ontology, DOID_6682) |
| External Link | http://compbio.charite.de/hpoweb/showterm?id=HP:0003302 |
| Similar Terms | |
| Downloads & Tools |
9 genes associated with the spondylolisthesis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| AGA | aspartylglucosaminidase |
| CTSK | cathepsin K |
| FBN1 | fibrillin 1 |
| KANSL1 | KAT8 regulatory NSL complex subunit 1 |
| MAN2B1 | mannosidase, alpha, class 2B, member 1 |
| RUNX2 | runt-related transcription factor 2 |
| SMAD3 | SMAD family member 3 |
| TGFB2 | transforming growth factor, beta 2 |
| ZNF469 | zinc finger protein 469 |
