ORPHA:619953
Familial hyperinflammatory lymphoproliferative immunodeficiency
Also called HEM1 deficiency syndrome, NCKAP1L-associated hyperinflammatory disorder
- Body system
- Immunological diseases
- Inheritance pattern
- Autosomal recessive
- Typical age of onset
- Childhood, Infancy, Neonatal
- Estimated prevalence
- <1 / 1 000 000 (Worldwide)
- Rarity class
- <1 / 1 000 000
ORPHA:619953 is classified under "Immunological diseases" in the Orphanet nomenclature.