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.
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.
Disease data
Classification
Disease
Synonyms
Bonneau-Beaumont syndrome
HHCS
Zespół hiperferrytemia dziedziczna-zaćma
Zespół Bonneau i Beaumont
HHCS
Hereditary hyperferritinemia with congenital cataracts
ORPHA code
163
OMIM code
600886
ICD10 code
H26.0
ICD11 code
-
No additional description.
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