facial palsy secondary to cranial hyperostosis Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Paralysis of the facial nerves on the basis of overgrowth of the cranial bones causing impingement upon the seventh cranial nerve. (Human Phenotype Ontology, HP_0007285)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0007285
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Genes

1 genes associated with the facial palsy secondary to cranial hyperostosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
SOST sclerostin