OBO ID: DOID:0111370 |
Term Name: | apolipoprotein C-III deficiency | Search Ontology: | |
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Synonyms: |
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Definition: | A cholesterol-ester transfer protein deficiency characterized by elevated levels of alpha-lipoprotein in the blood that has_material_basis_in heterozygous mutation in the APOC3 gene on chromosome 11q23.3. https://www.ncbi.nlm.nih.gov/pubmed/2022742 | ||
References: | |||
Ontology: | Human Disease ( DOID:0111370 ) |
OTHER apolipoprotein C-III deficiency PAGES
GENES INVOLVED
Human Gene | Zebrafish Ortholog | OMIM Term | OMIM Phenotype ID |
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APOC3 | Apolipoprotein C-III deficiency |
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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