ORPHA:319563

Mendelian susceptibility to mycobacterial diseases due to complete ISG15 deficiency

Also called MSMD due to complete ISG15 deficiency

Body system

Immunological diseases

Inheritance pattern

Autosomal recessive

Typical age of onset

Childhood

Estimated prevalence

<1 / 1 000 000 (Worldwide)

Rarity class

<1 / 1 000 000

ORPHA:319563 is classified under "Immunological diseases" in the Orphanet nomenclature.