MONDO_0009452 (Vici syndrome) is a very rare and severe congenital multisystem disorder characterized by the principal features of agenesis of the corpus callosum, cataracts, oculocutaneous hypopigmentation, cardiomyopathy and combined immunodeficiency. Also known as: Dionisi-Vici-Sabetta-Gambarara syndrome, absent corpus callosum-cataract-immunodeficiency syndrome, corpus callosum agenesis-cataract-immunodeficiency syndrome, immunodeficiency with cleft lip/palate, cataract, hypopigmentation, and absent corpus callosum.