ORPHA:688543
T-B-NK- reticular dysgenesis-like severe combined immunodeficiency
Also called Activated RAC2-associated severe combined immunodeficiency, Activated Rac2 defect, Non-syndromic reticular dysgenesis, T-B-NK- reticular dysgenesis-like SCID
- Body system
- Immunological diseases
- Inheritance pattern
- Autosomal dominant
- Typical age of onset
- Not documented in Orphadata
- Estimated prevalence
- Not documented in Orphadata
- Rarity class
- Not documented in Orphadata
ORPHA:688543 is classified under "Immunological diseases" in the Orphanet nomenclature.