pseudobulbar paralysis Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0007024
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Genes

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

Symbol Name
CYP27A1 cytochrome P450, family 27, subfamily A, polypeptide 1
LMNB1 lamin B1
NOTCH3 notch 3
SOD1 superoxide dismutase 1, soluble