Immundefekt, kombinierter schwerer, durch FOXN1-Defizienz
ORPHA:169095· ICD-10 D82.8· Severe combined immunodeficiency due to FOXN1 deficiency
- Prävalenz
- <1 / 1 000 000
- Vererbung
- Autosomal recessive
- Erkrankungsalter
- Infancy, Neonatal
ORPHA:169095· ICD-10 D82.8· Severe combined immunodeficiency due to FOXN1 deficiency