autonomic dysregulation Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormality of the regulation of the autonomic nervous system. (Human Phenotype Ontology, HP_0002271)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0002271
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Genes

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

Symbol Name
EDNRB endothelin receptor type B
SOX10 SRY (sex determining region Y)-box 10