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hypoalphalipoproteinemia
(phenotype)
Summary
General Info
Genetic Markers
Most Correlated Genes
Most Correlated SNPs
LCAT
APOA1
HDLCQ14
No SNPs found
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Pathway Enrichment
Most Correlated Biogroups
GNF2_TST
ACEVEDO_LIVER_TUMOR_VS_NORMAL_ADJACENT_TISSUE_DN
CAIRO_LIVER_DEVELOPMENT_DN
CAIRO_HEPATOBLASTOMA_DN
HSIAO_LIVER_SPECIFIC_GENES
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Curated Studies
Most Correlated Studies
Mouse Phenotypes - Familial lipoprotein deficiency
Mouse Phenotypes - Lecithin cholesterol acyltransferase deficiency
OMIM - Congenital disorder
OMIM - Hypoalphalipoproteinaemia
OMIM - Tangier disease
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Literature
Most Relevant Literature
Whole-exome sequencing reveals damaging gene variants associated with hypoalphalipoproteinemia.
Large-scale deletions of the ABCA1 gene in patients with hypoalphalipoproteinemia.
Effect of open-label infusion of an apoA-I-containing particle (CER-001) on RCT and artery wall thic…
Targeted Proteomics Identifies Paraoxonase/Arylesterase 1 (PON1) and Apolipoprotein Cs as Potential …
Effect of a common missense variant in LIPA gene on fatty liver disease and lipid phenotype: New per…
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Clinical Trials
Most Relevant Clinical Trials
CER-001 Therapy as a Novel Approach to Treat Genetic Orphan Diseases
Short-term Effect of Extended-release Niacin on Endothelial Function.
Tomato Consumption and High Density Lipoprotein-cholesterol
Quantitative Genetic Analysis of Lipid Research Clinic Family Data
High-Density Lipoprotein (HDL) Treatment Study
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