aplasia/hypoplasia of the cervical spine Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Aplasia or developmental hypoplasia of the cervical vertebral column. (Human Phenotype Ontology, HP_0011041)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0011041
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Genes

3 genes associated with the aplasia/hypoplasia of the cervical spine phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
FLNB filamin B, beta
SLC26A2 solute carrier family 26 (anion exchanger), member 2
SOX9 SRY (sex determining region Y)-box 9