abnormal basal ganglia mri signal intensity Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A deviation from normal signal on magnetic resonance imaging (MRI) of the basal ganglia. (Human Phenotype Ontology, HP_0012751)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0012751
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Genes

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.

Symbol Name
ETHE1 ethylmalonic encephalopathy 1