anarthria Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A defect in the motor ability that enables speech. (Human Phenotype Ontology, HP_0002425)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0002425
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Genes

3 genes associated with the anarthria phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ALS2 amyotrophic lateral sclerosis 2 (juvenile)
ATP13A2 ATPase type 13A2
FTL ferritin, light polypeptide