|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||A deviation from normal signal on magnetic resonance imaging (MRI) of the basal ganglia. (Human Phenotype Ontology, HP_0012751)|
|Downloads & Tools|
1 genes associated with the abnormal basal ganglia mri signal intensity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
|ETHE1||ethylmalonic encephalopathy 1|