Apolipoprotein C-iii Deficiency

Clinical Features

Phenotypes and symptoms related to Apolipoprotein C-iii Deficiency

  • Decreased LDL cholesterol concentration
  • Increased HDL cholesterol concentration
  • Hypotriglyceridemia

Incidence and onset information

— Currently we don't have prevalence information about this disease (Not enough data available about incidence and published cases.)
No data available about the known clinical features onset.

Alternative names

Apolipoprotein C-iii Deficiency Is also known as hyperalphalipoproteinemia 2, halp2.

Researches and researchers

Currently, we don't have any information about doctors, researches or researchers related to this disease. Please contact us if you would like to appear here.

Apolipoprotein C-iii Deficiency Recommended genes panels

Panel Name, Specifity and genes Tested/covered
APOC3.

By Institute for Human Genetics University Clinic Freiburg (Germany).

APOC3
Specificity
100 %
Genes
100 %
Dyslipidemia NGS panel (29 genes), Sequence & CNV analysis.

By Laboratory of genome diagnostics Academic Medical Center, University of Amsterdam (Netherlands).

SAR1B, SLCO1B1, ABCG5, ABCG8, LMF1, SCARB1, APOA5, LDLRAP1, CETP, PCSK9, MYLIP, STAP1, GPIHBP1, CYP27A1, CYP7A1, ANGPTL3, APOC2, APOC3, APOE, LCAT , (...)

View the complete list with 5 more genes
Specificity
4 %
Genes
100 %
APOC3. Complete sequencing.

By Instituto de Medicina Genomica Instituto de Medicina Genomica (Spain).

APOC3
Specificity
100 %
Genes
100 %
Hyperalphalipoproteinemia 2.

By Laboratory for Molecular Diagnostics Center for Nephrology and Metabolic Disorders (Germany).

APOC3
Specificity
100 %
Genes
100 %
Inherited Cardiovascular Diseases and Sudden Death Panel.

By Health in Code (Spain).

MRPL3, RYR2, SCN10A, SCN1B, SCN2B, SCN4B, SCN5A, BMPR1B, BMPR2, SGCA, SGCB, SGCD, SKI, SLC22A5, BRAF, SLC25A4, SNTA1, SOS1, SURF1, TAZ , (...)

View the complete list with 191 more genes
Specificity
1 %
Genes
100 %
Cardiovascular Diseases_General Panel.

By Health in Code (Spain).

RIT1, MRPL3, RRAS, RYR1, RYR2, SAR1B, BLK, SCN10A, SCN1B, SCN2B, SCN4B, SCN5A, SCO2, SDHA, BMPR1A, BMPR1B, BMPR2, SGCA, SGCB, SGCD , (...)

View the complete list with 351 more genes
Specificity
1 %
Genes
100 %
Dyslipidemias / Early atherosclerosis.

By Health in Code (Spain).

RYR1, SAR1B, BLK, SLCO1B1, SLC22A8, SLC2A2, HNF1A, HNF1B, KLF11, WFS1, ZMPSTE24, NEUROG3, ABCG5, ABCG8, LMF1, PCDH15, CAV1, BSCL2, SCARB1, TRIB1 , (...)

View the complete list with 57 more genes
Specificity
2 %
Genes
100 %
Primary familial hypertriglyceridemias.

By Health in Code (Spain).

LMF1, PCDH15, TRIB1, APOA5, GPIHBP1, SLC25A40, PNPLA2, GPD1, APOC2, APOC3, APOE
Specificity
10 %
Genes
100 %

You can get up to 6 more panels with our dedicated tool

Learn more

Sources and references

You can check the following sources for additional information.

MESH OMIM Rare Disease Symptoms Checker

If you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like STARGARDT DISEASE SPINOCEREBELLAR ATAXIA 41; SCA41 INTELLECTUAL DEVELOPMENTAL DISORDER WITH PERSISTENCE OF FETAL HEMOGLOBIN METACHONDROMATOSIS; METCDS EPSTEIN SYNDROME; EPSTNS EHLERS-DANLOS SYNDROME TYPE 7A CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IB; ARCL1B