A hemochromatosis that has_material_basis_in heterozygous mutation in the FTH1 gene on chromosome 11q12. [ url:https://www.ncbi.nlm.nih.gov/pubmed/11389486 http://purl.obolibrary.org/obo/ECO_0007645 ]

Synonyms: FTH1-associated iron overload FTH1-related iron overload HFE5

This is just here as a test because I lose it

Term information

database cross reference
  • MIM:615517
  • ORDO:247790
  • ICD10CM:E83.1
Subsets

DO_rare_slim

acronym
HFE5

has obo namespace

disease_ontology

id

DOID:0111031