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bn:25337925n
Noun Named Entity
PT
No term available
EN
Hemochromatosis that has material basis in heterozygous mutation in the FTH1 gene on chromosome 11q12 Wikidata
Relations
Sources
IS A
doença
doença rara
doença genética
EN
HFE hereditary haemochromatosis
GENETIC ASSOCIATION
FTH1

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