Osteopetrose-Hypogammaglobulinämie-Syndrom
ORPHA:178389· ICD-10 Q78.2· Osteopetrosis-hypogammaglobulinemia syndrome
- Prävalenz
- <1 / 1 000 000
- Vererbung
- Autosomal recessive
- Erkrankungsalter
- Infancy, Neonatal
ORPHA:178389· ICD-10 Q78.2· Osteopetrosis-hypogammaglobulinemia syndrome