Monarch Disease Ontology entry MONDO_0013751 (cutis laxa, autosomal dominant 2) is any autosomal dominant cutis laxa in which the cause of the disease is a mutation in the FBLN5 gene. Also known as: FBLN5 autosomal dominant cutis laxa, autosomal dominant cutis laxa 2, autosomal dominant cutis laxa caused by mutation in FBLN5, cutis laxa, autosomal dominant type 2.