Hereditary hyperferritinemia-cataract syndrome
ORPHA:163· ICD-10 H26.0
Definition
A rare genetic disease characterized by the association of early onset cataract with persistently raised plasma ferritin concentrations in the absence of iron overload.
- Prevalence
- <1 / 1 000 000
- Inheritance
- Autosomal dominant
- Age of onset
- All ages