c2-c3 subluxation Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A partial dislocation of the intervertebral joint between the second and third cervical vertebrae. (Human Phenotype Ontology, HP_0008456)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0008456
Similar Terms
Downloads & Tools

Genes

1 genes associated with the c2-c3 subluxation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
FLNB filamin B, beta