ORPHA:319581

Autosomal dominant mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR1 deficiency

Also called Autosomal dominant MSMD due to partial IFNgammaR1 deficiency, Autosomal dominant MSMD due to partial interferon gamma receptor 1 deficiency, Autosomal dominant mendelian susceptibility to mycobacterial diseases due to partial interferon gamma receptor 1 deficiency

Body system

Immunological diseases

Inheritance pattern

Autosomal dominant

Typical age of onset

Adolescent

Estimated prevalence

<1 / 1 000 000 (Worldwide)

Rarity class

<1 / 1 000 000

ORPHA:319581 is classified under "Immunological diseases" in the Orphanet nomenclature.