ORPHA:209

Cutis laxa

Body system

Skin diseases

Inheritance pattern

Autosomal dominant, Autosomal recessive, Not applicable, X-linked recessive

Typical age of onset

Not documented in Orphadata

Estimated prevalence

1-9 / 1 000 000 (Europe)

Rarity class

1-9 / 1 000 000

ORPHA:209 is classified under "Skin diseases" in the Orphanet nomenclature.