basilar impression Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Abnormal elevation of the floor of the posterior fossa including occipital condyles and foramen magnum. (Human Phenotype Ontology, HP_0005758)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0005758
Similar Terms
Downloads & Tools

Genes

4 genes associated with the basilar impression phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
COL1A1 collagen, type I, alpha 1
COL1A2 collagen, type I, alpha 2
NOTCH2 notch 2
ZBTB20 zinc finger and BTB domain containing 20