ORPHA:313838

Coats plus syndrome

Also called CRMCC, Cerebroretinal microangiopathy with calcifications and cysts

Body system

Immunological diseases

Inheritance pattern

Autosomal recessive

Typical age of onset

Childhood

Estimated prevalence

<1 / 1 000 000 (Europe)

Rarity class

<1 / 1 000 000

ORPHA:313838 is classified under "Immunological diseases" in the Orphanet nomenclature.