ORPHA:183707

Infantile LAD-like disease due to RAC2 deficiency

Also called Infantile leukocyte adhesion deficiency due to Rac family small GTPase 2 deficiency

Body system

Immunological diseases

Inheritance pattern

Autosomal dominant

Typical age of onset

Infancy, Neonatal

Estimated prevalence

<1 / 1 000 000 (Worldwide)

Rarity class

<1 / 1 000 000

ORPHA:183707 is classified under "Immunological diseases" in the Orphanet nomenclature.