ORPHA:228003
T-B+NK+ severe combined immunodeficiency due to CORO1A deficiency
Also called T-B+NK+ SCID due to CORO1A deficiency, T-B+NK+ SCID due to coronin-1A deficiency, T-B+NK+ severe combined immunodeficiency due to coronin-1A deficiency
- Body system
- Immunological diseases
- Inheritance pattern
- Autosomal recessive
- Typical age of onset
- Childhood, Infancy, Neonatal
- Estimated prevalence
- <1 / 1 000 000 (Worldwide)
- Rarity class
- <1 / 1 000 000
ORPHA:228003 is classified under "Immunological diseases" in the Orphanet nomenclature.