Vici syndrome

MONDO:0009452

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, Vici syndrome, absent corpus callosum-cataract-immunodeficiency syndrome, corpus callosum agenesis-cataract-immunodeficiency syndrome, immunodeficiency with cleft lip/palate, cataract, hypopigmentation, and absent corpus callosum, Dionisi Vici Sabetta Gambarara syndrome, VICIS, absent corpus callosum cataract immunodeficiency

0 clinical trials for this condition and its sub-types, 0 tagged with Vici syndrome itself.

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↑ Immune system disorder (12959) ↑ Syndromic disease (7133) ↑ Autosomal recessive disease (994) ↑ Multiple congenital anomalies/dysmorphic syndrome without intellectual disability (163)

Including sub-types (0) Tagged with Vici syndrome (0)

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