|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||Compression of the spinal cord in the cervical region, generally manifested by paresthesias and numbness, weakness, difficulty walking, abnormalities of coordination, and neck pain or stiffness. (Human Phenotype Ontology, HP_0002341)|
|Downloads & Tools|
3 genes associated with the cervical cord compression phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.