ORPHA:319589

Autosomal dominant mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR2 deficiency

Also called Autosomal dominant MSMD due to partial IFNgammaR2 deficiency, Autosomal dominant MSMD due to partial interferon gamma receptor 2 deficiency, Autosomal dominant mendelian susceptibility to mycobacterial diseases due to partial interferon gamma receptor 2 deficiency

Body system

Immunological diseases

Inheritance pattern

Autosomal dominant

Typical age of onset

Infancy

Estimated prevalence

<1 / 1 000 000 (Worldwide)

Rarity class

<1 / 1 000 000

ORPHA:319589 is classified under "Immunological diseases" in the Orphanet nomenclature.