ORPHA:481662

Familial Chilblain lupus

Body system

Skin diseases

Inheritance pattern

Autosomal dominant

Typical age of onset

Childhood, Infancy

Estimated prevalence

<1 / 1 000 000 (Worldwide)

Rarity class

<1 / 1 000 000

ORPHA:481662 is classified under "Skin diseases" in the Orphanet nomenclature.