cerebral dysmyelination Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Defective structure and function of myelin sheaths of the white matter of the brain. (Human Phenotype Ontology, HP_0007266)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0007266
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Genes

7 genes associated with the cerebral dysmyelination phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ADGRG1 adhesion G protein-coupled receptor G1
HSD17B4 hydroxysteroid (17-beta) dehydrogenase 4
MCOLN1 mucolipin 1
PHGDH phosphoglycerate dehydrogenase
PLP1 proteolipid protein 1
PSAP prosaposin
SOX10 SRY (sex determining region Y)-box 10