megalencephaly-capillary malformation-polymicrogyria syndrome, somatic Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://www.omim.org/entry/602501
Similar Terms
Downloads & Tools

Genes

1 genes associated with the megalencephaly-capillary malformation-polymicrogyria syndrome, somatic phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
PIK3CA phosphatidylinositol-4,5-bisphosphate 3-kinase, catalytic subunit alpha