OBO ID: DOID:0111032 |
Term Name: | hemochromatosis type 2B | Search Ontology: | |
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Definition: | A hemochromatosis type 2 that has_material_basis_in homozygous mutation in the HAMP gene on chromosome 19q13. https://www.ncbi.nlm.nih.gov/pubmed/12469120 | ||
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Ontology: | Human Disease ( DOID:0111032 ) |
OTHER hemochromatosis type 2B PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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