ORPHA:317476
XMEN
Also called CID due to MAGT1 deficiency, Combined immunodeficiency due to MAGT1 deficiency, X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection and neoplasia
- Body system
- Immunological diseases
- Inheritance pattern
- X-linked recessive
- Typical age of onset
- Adolescent, Adult, Childhood
- Estimated prevalence
- <1 / 1 000 000 (Worldwide)
- Rarity class
- <1 / 1 000 000
ORPHA:317476 is classified under "Immunological diseases" in the Orphanet nomenclature.