Charcot-Marie-Tooth disease, demyelinating, 1H (CMT1H) [130]; Cutis laxa, autosomal dominant, 2 (ADCL2) [131]; Cutis laxa, autosomal recessive, 1A (ARCL1A) [132]; Macular degeneration, age-related, 3 (ARMD3) [133]. The gene discussed is FBLN5; the disease is autosomal dominant cutis laxa.