ORPHA:319558
Mendelian susceptibility to mycobacterial diseases due to complete IL12B deficiency
Also called MSMD due to complete IL12B deficiency, MSMD due to complete interleukin 12B deficiency, Mendelian susceptibility to mycobacterial diseases due to complete interleukin 12B deficiency
- Body system
- Immunological diseases
- Inheritance pattern
- Autosomal recessive
- Typical age of onset
- Infancy, Neonatal
- Estimated prevalence
- <1 / 1 000 000 (Worldwide)
- Rarity class
- <1 / 1 000 000
ORPHA:319558 is classified under "Immunological diseases" in the Orphanet nomenclature.