hereditary haemochromatosis
MeSH: D006432ORPHA: 139498
Overview
metal metabolism disorder characterized by the accumulation of iron in various organs of the body
Available Treatments (0)
No treatments linked yet
Clinical trials or compassionate use may be available — consult a specialist.
Classification & Codes
MeSH Code
D006432Orphanet Code
ORPHA:139498hereditary haemochromatosis
| MeSH | D006432 |
| Orphanet | ORPHA:139498 |
| Treatments | 0 drug(s) |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO