Kalıtsal hiperferritinemi-katarakt sendromu
ORPHA:163· ICD-10 H26.0· Hereditary hyperferritinemia-cataract syndrome
- Yaygınlık
- <1 / 1 000 000
- Kalıtım
- Autosomal dominant
- Başlangıç yaşı
- All ages
ORPHA:163· ICD-10 H26.0· Hereditary hyperferritinemia-cataract syndrome