Search Ontology:
Human Disease
primary hypoalphalipoproteinemia 2
- Term ID
- DOID:0080958
- Synonyms
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- Apolipoprotein A-I deficiency
- Definition
- A hypolipoproteinemia that is characterized by dysfunctional apoA-I production, resulting in undetectable levels of apoA-I in serum and in markedly low levels of serum high density lipoprotein cholesterol, is generally an autosomal recessive disorder associated with extensive atherosclerosis, xanthomas, and corneal opacities, and that has_material_basis_in homozygous, compound heterozygous, or heterozygous mutation in the APOA1 gene on chromosome 11q23. https://pubmed.ncbi.nlm.nih.gov/29396262/
- References
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- GARD:758
- MIM:618463
- ORDO:425
- Ontology
- Human Disease ( DOID:0080958 )
- is a type of
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Genes Involved
Zebrafish Models