peripheral hypermyelination Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Increased amount of peripheral myelination. (Human Phenotype Ontology, HP_0030173)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0030173
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Genes

5 genes associated with the peripheral hypermyelination phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
MPZ myelin protein zero
MTMR2 myotubularin related protein 2
NEFL neurofilament, light polypeptide
PMP22 peripheral myelin protein 22
SOX10 SRY (sex determining region Y)-box 10