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Hemochromatosis type 4

^ http://www.orpha.net/ORDO/Orphanet_139491


Hemochromatosis type 4 (also called ferroportin disease) is a form of rare hereditary hemochromatosis (HH; see this term), a group of diseases characterized by excessive tissue iron deposition of genetic origin.

Synonyms: Ferroportin disease, Autosomal dominant hereditary hemochromatosis, Hemochromatosis due to defect in ferroportin

Term info

database cross reference
  • UMLS:C1853733 (E (exact mapping (the terms and the concepts are equivalent)))
  • OMIM:606069 (E (exact mapping (the terms and the concepts are equivalent)))
  • MeSH:C537249 (E (exact mapping (the terms and the concepts are equivalent)))
  • ICD-10:E83.1 (Attributed)
  • ICD-10:E83.1 (NTBT (narrower term maps to a broader term))
hasDbXref

UMLS:C1853733, MeSH:C537249, OMIM:606069, ICD-10:E83.1

notation

ORPHA:139491