pontocerebellar atrophy Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Atrophy affecting the pons and the cerebellum. (Human Phenotype Ontology, HP_0006879)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0006879
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Genes

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

Symbol Name
DPM1 dolichyl-phosphate mannosyltransferase polypeptide 1, catalytic subunit
SETX senataxin