ORPHA:437552
Autosomal recessive primary immunodeficiency with defective spontaneous natural killer cell cytotoxicity
Also called Autosomal recessive primary immunodeficiency with defective spontaneous NK cell cytotoxicity, CD16 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:437552 is classified under "Immunological diseases" in the Orphanet nomenclature.