MONDO_0012195 (arthrogryposis-severe scoliosis syndrome) can be described as follows. Distal arthrogryposis type 4 is an inherited developmental defect syndrome characterized by multiple congenital contractures of limbs, without primary neurologic and/or muscle disease that affects limb function, and a mild to severe scoliosis. Intelligence is normal. Also known as: distal arthrogryposis type 4, distal arthrogryposis type IID.