Toriello-Carey syndrome (Monarch Disease Ontology term MONDO_0009021) can be described as follows. Toriello Carey syndrome is a multiple congenital anomaly syndrome characterized by craniofacial dysmorphic features, cerebral anomalies, swallowing difficulties, cardiac defects and hypotonia. Also known as: corpus callosum agenesis-blepharophimosis-Robin sequence syndrome.