ORPHA:1451

CINCA syndrome

Also called Chronic infantile neurological cutaneous and articular syndrome, IOMID syndrome, Infantile-onset multisystem inflammatory disease, NOMID syndrome, Neonatal-onset multisystem inflammatory disease, Prieur-Griscelli syndrome

Body system

Immunological diseases

Inheritance pattern

Autosomal dominant, Not applicable

Typical age of onset

Infancy, Neonatal

Estimated prevalence

Unknown (Worldwide)

Rarity class

Unknown

ORPHA:1451 is classified under "Immunological diseases" in the Orphanet nomenclature.