ORPHA:277
T-B-NK- severe combined immunodeficiency due to adenosine deaminase deficiency
Also called ADA deficiency, T-B-NK- SCID due to adenosine deaminase deficiency
- Body system
- Inborn errors of metabolism
- Inheritance pattern
- Autosomal recessive
- Typical age of onset
- Infancy, Neonatal
- Estimated prevalence
- 1-9 / 1 000 000 (Europe)
- Rarity class
- 1-9 / 1 000 000
ORPHA:277 is classified under "Inborn errors of metabolism" in the Orphanet nomenclature.
Common signs
- Sinusitis
- Recurrent otitis media
- Failure to thrive
- Lymphopenia
- Diarrhea
- Recurrent upper respiratory tract infections