Ferroportin deficiency

Synonym(s)
- Hereditary hemochromatosis type 4,
- ferroportin disease
Type

Disease
External link(s)
- Orphanet
- IEMbase
Gene
- SLC40A1 / solute carrier family 40 member 1
  2q32.2
  OMIM
  GnomAD
  Ensembl
  HGNC
  VMH
  LOVD
Gene product
- Ferroportin
Disease group(s)
- 22.2 Disorders of iron metabolism
Child entries
- SLC40A1-related hemochromatosis