ORPHA:86788
X-linked severe congenital neutropenia
- Body system
- Immunological diseases
- Inheritance pattern
- X-linked recessive
- Typical age of onset
- Infancy, Neonatal
- Estimated prevalence
- <1 / 1 000 000 (Worldwide)
- Rarity class
- <1 / 1 000 000
ORPHA:86788 is classified under "Immunological diseases" in the Orphanet nomenclature.
Common signs
- Decreased total neutrophil count
- Recurrent bacterial infections
- Monocytopenia