echolalia Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A speech disorder that involves the automatic repetition of vocalizations made by another person. (Human Disease Ontology, DOID_4188)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0010529
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Genes

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

Symbol Name
MAPT microtubule-associated protein tau
PSEN1 presenilin 1
SLITRK1 SLIT and NTRK-like family, member 1
UBE2A ubiquitin-conjugating enzyme E2A