|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||An abnormality related to a defect of vertebral separation of cervical vetebrae during development. (Human Phenotype Ontology, HP_0004632)|
|Downloads & Tools|
1 genes associated with the cervical segmentation defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
|FLNB||filamin B, beta|