Phakomatosis Cesioflammea, also known as phakomatosis pigmentovascularis type 2, is related to capillary malformations, congenital and phakomatosis pigmentovascularis. An important gene associated with Phakomatosis Cesioflammea is GNA11 (G Protein Subunit Alpha 11), and among its related pathways/superpathways are Development Angiotensin activation of ERK and Calmodulin induced events. Affiliated tissues include skin and eye.