Ogden Syndrome (OGDNS)

Ogden Syndrome, also known as n-terminal acetyltransferase deficiency, is related to microphthalmia, syndromic 1 and aortic aneurysm, familial abdominal, 1. An important gene associated with Ogden Syndrome is NAA10 (N-Alpha-Acetyltransferase 10, NatA Catalytic Subunit), and among its related pathways/superpathways is Ac/N-end rule pathway. Affiliated tissues include skin and testis, and related phenotypes are scoliosis and global developmental delay