ORPHA:238505
Combined immunodeficiency due to CD27 deficiency
Also called Autosomal recessive lymphoproliferative disease due to CD27 deficiency, CD27 deficiency
- Body system
- Immunological diseases
- Inheritance pattern
- Autosomal recessive
- Typical age of onset
- Adolescent, Adult, Childhood, Infancy
- Estimated prevalence
- <1 / 1 000 000 (Worldwide)
- Rarity class
- <1 / 1 000 000
ORPHA:238505 is classified under "Immunological diseases" in the Orphanet nomenclature.