frontoparietal polymicrogyria Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An excessive number of small gyri (convolutions) on the surface of the brain in the frontoparietal region. (Human Phenotype Ontology, HP_0007095)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0007095
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Genes

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

Symbol Name
ADGRG1 adhesion G protein-coupled receptor G1
SRPX2 sushi-repeat containing protein, X-linked 2
TBC1D20 TBC1 domain family, member 20