abnormality of the striatum Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Abnormality of the striatum (FMA:77618). (Human Phenotype Ontology, HP_0010994)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0010994
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Genes

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

Symbol Name
TREM2 triggering receptor expressed on myeloid cells 2
TYROBP TYRO protein tyrosine kinase binding protein
VPS13A vacuolar protein sorting 13 homolog A (S. cerevisiae)