deep white matter hypodensities Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Multiple areas of darker than expected signal on magnetic resonance imaging emanating from the deep cerebral white matter. (Human Phenotype Ontology, HP_0007321)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0007321
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Genes

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

Symbol Name
TREX1 three prime repair exonuclease 1