severe demyelination of the white matter Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A severe loss of myelin from nerve fibers in the central nervous system. (Human Phenotype Ontology, HP_0007258)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0007258
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Genes

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

Symbol Name
L2HGDH L-2-hydroxyglutarate dehydrogenase