Kombinovaná imunodeficience způsobená haploinsuficiencí FOXN1
ORPHA:676039· ICD-10 D81.8· Combined immunodeficiency due to FOXN1 haploinsufficiency
- Prevalence
- <1 / 1 000 000
- Dědičnost
- Autosomal dominant
- Věk nástupu
- Childhood, Infancy, Neonatal
ORPHA:676039· ICD-10 D81.8· Combined immunodeficiency due to FOXN1 haploinsufficiency