ORPHA:99898

Mendelian susceptibility to mycobacterial diseases due to complete IFNgammaR1 deficiency

Also called MSMD due to complete IFNgammaR1 deficiency, MSMD due to complete interferon gamma receptor 1 deficiency, Mendelian susceptibility to mycobacterial diseases due to complete interferon gamma receptor 1 deficiency

Body system

Immunological diseases

Inheritance pattern

Autosomal recessive

Typical age of onset

Infancy, Neonatal

Estimated prevalence

<1 / 1 000 000 (Worldwide)

Rarity class

<1 / 1 000 000

ORPHA:99898 is classified under "Immunological diseases" in the Orphanet nomenclature.