peripheral dysmyelination Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Defective structure and function of myelin sheaths. Dysmyelination is distinguished from demyleination where there is destruction or damage of previously normal myelination. (Human Phenotype Ontology, HP_0003469)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0003469
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Genes

2 genes associated with the peripheral dysmyelination 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