OBO ID: DOID:0111031 |
Term Name: | hemochromatosis type 5 | Search Ontology: | |
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Definition: | A hemochromatosis that has_material_basis_in heterozygous mutation in the FTH1 gene on chromosome 11q12. https://www.ncbi.nlm.nih.gov/pubmed/11389486 | ||
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Ontology: | Human Disease ( DOID:0111031 ) |
OTHER hemochromatosis type 5 PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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