|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||A darker than expected signal on magnetic resonance imaging emanating from the cerebral white matter. (Human Phenotype Ontology, HP_0007103)|
|Downloads & Tools|
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.