Osteopetroz-hipogammaglobulinemi sendromu
ORPHA:178389· ICD-10 Q78.2· Osteopetrosis-hypogammaglobulinemia syndrome
- Yaygınlık
- <1 / 1 000 000
- Kalıtım
- Autosomal recessive
- Başlangıç yaşı
- Infancy, Neonatal
ORPHA:178389· ICD-10 Q78.2· Osteopetrosis-hypogammaglobulinemia syndrome