ORPHA:477857

Mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency

Also called MSMD due to complete RORgamma receptor defiency, Mendelian susceptibility to mycobacterial diseases due to complete RAR related orphan receptor C deficiency, Primary immunodeficiency due to RORC mutation

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:477857 is classified under "Immunological diseases" in the Orphanet nomenclature.