ORPHA:720371

T-B+NK+ severe combined immunodeficiency due to LCP2 deficiency

Body system

Immunological diseases

Inheritance pattern

Autosomal recessive

Typical age of onset

Infancy, Neonatal

Estimated prevalence

<1 / 1 000 000 (Worldwide)

Rarity class

<1 / 1 000 000

ORPHA:720371 is classified under "Immunological diseases" in the Orphanet nomenclature.