Temtamy syndrome is a very rare congenital genetic neurological disorder characterized by agenesis/hypoplasia of corpus callosum with developmental abnormalities, ocular disorders, and variable craniofacial and skeletal abnormalities. The disease is MONDO_0009033 (temtamy syndrome). Also known as: Temtamy-Shalash syndrome, craniofacial dysmorphism-coloboma-corpus callosum agenesis syndrome.