cavitation of the basal ganglia Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description The formation of small cavities in the tissue of the basal ganglia. (Human Phenotype Ontology, HP_0007007)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0007007
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Genes

1 genes associated with the cavitation of the basal ganglia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
FTL ferritin, light polypeptide