ORPHA:504523
T-B+NK+ severe combined immunodeficiency due to LAT deficiency
Also called T-B+NK+ SCID due to LAT deficiency
- Body system
- Immunological diseases
- Inheritance pattern
- Autosomal recessive
- Typical age of onset
- Infancy
- Estimated prevalence
- <1 / 1 000 000 (Worldwide)
- Rarity class
- <1 / 1 000 000
ORPHA:504523 is classified under "Immunological diseases" in the Orphanet nomenclature.