O'donnell-Luria-Rodan Syndrome, also known as odluro, is related to contractures, pterygia, and spondylocarpotarsal fusion syndrome 1a and autism spectrum disorder. An important gene associated with O'donnell-Luria-Rodan Syndrome is KMT2E (Lysine Methyltransferase 2E (Inactive)). Affiliated tissues include skin and brain, and related phenotypes are seizure and epileptic encephalopathy