| Dataset | HPO Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | Abnormally increased movement at the junction between the first cervical (atlas) and the second cervical (axis) vertebrae as a result of either a bony or ligamentous anomaly. (Human Phenotype Ontology, HP_0003467) |
| External Link | http://compbio.charite.de/hpoweb/showterm?id=HP:0003467 |
| Similar Terms | |
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3 genes associated with the atlantoaxial instability phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
