hypointensity of cerebral white matter on mri Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A darker than expected signal on magnetic resonance imaging emanating from the cerebral white matter. (Human Phenotype Ontology, HP_0007103)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0007103
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4 genes associated with the hypointensity of cerebral white matter on mri phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
LAMA2 laminin, alpha 2
TREX1 three prime repair exonuclease 1
TYMP thymidine phosphorylase
UBE2A ubiquitin-conjugating enzyme E2A