Long Qt Syndrome 11 (LQT11)

Long Qt Syndrome 11, also known as lqt11, is related to benign familial neonatal epilepsy and deafness, autosomal recessive 98, and has symptoms including syncope An important gene associated with Long Qt Syndrome 11 is AKAP9 (A-Kinase Anchoring Protein 9), and among its related pathways/superpathways are Cardiac conduction and G-Beta Gamma Signaling. Affiliated tissues include heart, and related phenotypes are syncope and prolonged qtc interval