ORPHA:699615
Severe mendelian susceptibility to mycobacterial diseases due to complete IRF1 deficiency
Also called Severe MSMD due to complete IRF1 deficiency, Severe mendelian susceptibility to mycobacterial diseases due to complete interferon regulatory factor 1 deficiency
- Body system
- Immunological diseases
- Inheritance pattern
- Autosomal recessive
- Typical age of onset
- Not documented in Orphadata
- Estimated prevalence
- Not documented in Orphadata
- Rarity class
- Not documented in Orphadata
ORPHA:699615 is classified under "Immunological diseases" in the Orphanet nomenclature.