Nelymfoidní cystická dysgeneze brzlíku
ORPHA:169095· ICD-10 D82.8· Severe combined immunodeficiency due to FOXN1 deficiency
- Prevalence
- <1 / 1 000 000
- Dědičnost
- Autosomal recessive
- Věk nástupu
- Infancy, Neonatal
ORPHA:169095· ICD-10 D82.8· Severe combined immunodeficiency due to FOXN1 deficiency