hemochromatosis type 5
MeSH: C565020ORPHA: 247790
Overview
hemochromatosis that has material basis in heterozygous mutation in the FTH1 gene on chromosome 11q12
Available Treatments (0)
No treatments linked yet
Clinical trials or compassionate use may be available — consult a specialist.
Classification & Codes
MeSH Code
C565020Orphanet Code
ORPHA:247790hemochromatosis type 5
| MeSH | C565020 |
| Orphanet | ORPHA:247790 |
| Treatments | 0 drug(s) |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO