patchy demyelination of subcortical white matter Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Patchy loss of myelin from nerve fibers in the central nervous system. (Human Phenotype Ontology, HP_0002545)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0002545
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Genes

2 genes associated with the patchy demyelination of subcortical white matter phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ERCC6 excision repair cross-complementation group 6
ERCC8 excision repair cross-complementation group 8