abnormality of the coccyx Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormality of the coccyx. (Human Phenotype Ontology, HP_0008519)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0008519
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Genes

2 genes associated with the abnormality of the coccyx phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
TBX15 T-box 15
TRPV4 transient receptor potential cation channel, subfamily V, member 4