ORPHA:319569

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

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

Body system

Immunological diseases

Inheritance pattern

Autosomal recessive

Typical age of onset

Infancy

Estimated prevalence

<1 / 1 000 000 (Worldwide)

Rarity class

<1 / 1 000 000

ORPHA:319569 is classified under "Immunological diseases" in the Orphanet nomenclature.