ORPHA:183660

Severe combined immunodeficiency

Also called SCID

Body system

Immunological diseases

Inheritance pattern

Autosomal recessive, X-linked recessive

Typical age of onset

Infancy, Neonatal

Estimated prevalence

1-9 / 100 000 (Europe)

Rarity class

1-9 / 100 000

ORPHA:183660 is classified under "Immunological diseases" in the Orphanet nomenclature.