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General Information
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| Term |
primary hypoalphalipoproteinemia 1 |
ID (Ontology) |
DOID:0080957 (Human Disease) |
| Definition |
A hypolipoproteinemia that is characterized by low levels of high-density lipoprotein in the blood and that has_material_basis_in heterozygous mutation in the ABC1 gene on chromosome 9q31, which is also the site of mutations causing Tangier disease. |
| Also Known As |
"familial HDL deficiency" ; "familial hypoalphalipoproteinemia" |
| Comment |
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Links to External Ontologies
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DO.org
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Annotations
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Records annotated with this term OR any of its CHILD TERMS
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Records annotated with this exact term (annotations to child terms are NOT included)
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No relevant records available
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Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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| Full annotation statements | Relevant FlyBase reports |
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| Genes |
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primary hypoalphalipoproteinemia 1 | 3 | for disease ribbon | primary hypoalphalipoproteinemia 1 | 3 | model of | primary hypoalphalipoproteinemia 1 | 3 |
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Relationships