OBO ID: DOID:0111028
Term Name: hemochromatosis type 4 Search Ontology:
Synonyms:
  • autosomal dominant hereditary hemochromatosis
  • ferroportin disease
  • hemochromatosis due to defect in ferroportin
  • HFE4
Definition: A hemochromatosis that has_material_basis_in heterozygous mutation in the SLC40A1 gene on chromosome 2q32. https://www.ncbi.nlm.nih.gov/pubmed/11431687
References:
Ontology: Human Disease   (DOID:0111028)
OTHER hemochromatosis type 4 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
SLC40A1 Hemochromatosis, type 4 606069
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS (1)