OBO ID: DOID:3145 |
Term Name: | hyperlipoproteinemia type III | Search Ontology: | |
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Definition: | A familial hyperlipidemia that has_material_basis_in by homozygous, compound heterozygous, or heterozygous mutation in the APOE gene on chromosome 19q13. https://omim.org/entry/617347 | ||
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Ontology: | Human Disease ( DOID:3145 ) |
OTHER hyperlipoproteinemia type III PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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