ORPHA:699618
Severe mendelian susceptibility to mycobacterial diseases due to complete IFNG deficiency
Also called Severe MSMD due to complete IFNG deficiency, Severe mendelian susceptibility to mycobacterial diseases due to complete interferon gamma deficiency
- Body system
- Immunological diseases
- Inheritance pattern
- Autosomal recessive
- Typical age of onset
- Childhood, Infancy
- Estimated prevalence
- <1 / 1 000 000 (Worldwide)
- Rarity class
- <1 / 1 000 000
ORPHA:699618 is classified under "Immunological diseases" in the Orphanet nomenclature.