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DO Term : hemochromatosis type 4 [DOID:0111028] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A hemochromatosis that has_material_basis_in heterozygous mutation in the SLC40A1 gene on chromosome 2q32.
  • synonyms:
  • GARD:10094,
  • UMLS_CUI:C1853733,
  • 606069,
  • SNOMEDCT_US_2023_03_01:719975002,
  • ferroportin disease,
  • MESH:C537249,
  • OMIM:606069,
  • hemochromatosis due to defect in ferroportin,
  • ORDO:139491,
  • autosomal dominant hereditary hemochromatosis,
  • HFE4
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Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents





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