Rare diseases- Primary immunodeficiencies (PID)
- Familial hemophagocytic lymphohistiocytosis (FHL) syndromes without hypopigmentation
- STXBP2 / Munc18-2 deficiency (FHL5)
European Reference Network for Immunodeficiency, Autoinflammatory, Autimmune and Pediatric Rheumatic disea
- Rare diseases
- Primary immunodeficiencies (PID)
- Familial hemophagocytic lymphohistiocytosis (FHL) syndromes without hypopigmentation
- STXBP2 / Munc18-2 deficiency (FHL5)