multifocal cerebral white matter abnormalities Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0007052
Similar Terms
Downloads & Tools

Genes

1 genes associated with the multifocal cerebral white matter abnormalities phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
D2HGDH D-2-hydroxyglutarate dehydrogenase