ORPHA:99749
Kostmann syndrome
Also called Infantile agranulocytosis, Severe congenital neutropenia type 3
- Body system
- Immunological diseases
- Inheritance pattern
- Autosomal recessive
- Typical age of onset
- Neonatal
- Estimated prevalence
- <1 / 1 000 000 (Worldwide)
- Rarity class
- <1 / 1 000 000
ORPHA:99749 is classified under "Immunological diseases" in the Orphanet nomenclature.