ORPHA:1775

Dyskeratosis congenita

Also called DC, DKC, Zinsser-Engman-Cole syndrome

Body system

Immunological diseases

Inheritance pattern

Autosomal dominant, Autosomal recessive, X-linked recessive

Typical age of onset

Adolescent, Adult, Childhood, Infancy, Neonatal

Estimated prevalence

1-9 / 1 000 000 (Europe)

Rarity class

1-9 / 1 000 000

ORPHA:1775 is classified under "Immunological diseases" in the Orphanet nomenclature.