hereditary hyperferritinemia with congenital cataracts
MeSH: C538137ORPHA: 163
Overview
Hereditary hyperferritinemia with congenital cataracts is characterized by the association of early onset (although generally absent at birth) cataract with persistently raised plasma ferritin concentrations in the absence of iron overload
Available Treatments (0)
No treatments linked yet
Clinical trials or compassionate use may be available — consult a specialist.
Clinical Presentation
Signs and symptoms associated with hereditary hyperferritinemia with congenital cataracts, sourced from HPO and Orphanet clinical annotations.
CataractAbnormality of metabolism/homeostasis
Classification & Codes
MeSH Code
C538137Orphanet Code
ORPHA:163hereditary hyperferritinemia with congenital cataracts
| MeSH | C538137 |
| Orphanet | ORPHA:163 |
| Treatments | 0 drug(s) |
| Symptoms on record | 2 signs |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO