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Hemochromatosis type 4

MeSH: C537249ORPHA: 139491

Contents

  1. 1. Overview
  2. 2. Available Treatments
  3. 3. Classification & Codes

Overview

hemochromatosis that has material basis in heterozygous mutation in the SLC40A1 gene on chromosome 2q32

Available Treatments (0)

No treatments linked yet

Clinical trials or compassionate use may be available — consult a specialist.

Classification & Codes

MeSH Code

C537249

Orphanet Code

ORPHA:139491
Hemochromatosis type 4
MeSHC537249
OrphanetORPHA:139491
Treatments0 drug(s)
Statuspublished
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO