Distal arthrogryposis type 5 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 ocular anomalies (ptosis, external ophtalmoplegia and/or strabismus). Intelligence is normal. The disease is Monarch Disease Ontology entry MONDO_0007158 (arthrogryposis- oculomotor limitation-electroretinal anomalies syndrome). Also known as: distal arthrogryposis type 5, distal arthrogryposis type IIB, distal arthrogryposis with ophthalmoplegia, oculomelic amyoplasia.