ORPHA:169095

T-B+NK+ severe combined immunodeficiency due to FOXN1 deficiency

Also called T-B+NK+ SCID due to FOXN1 deficiency, Alymphoid cystic thymic dysgenesis, Nude/SCID, Nude/severe combined immunodeficiency, Severe T-cell immunodeficiency-congenital alopecia-nail dystrophy syndrome, Winged helix 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:169095 is classified under "Immunological diseases" in the Orphanet nomenclature.