Hyperalphalipoproteinemia 1; Halp1

Clinical Features

Phenotypes and symptoms related to Hyperalphalipoproteinemia 1; Halp1

  • Hypertension
  • Stroke
  • Abnormality of the cardiovascular system
  • Atherosclerosis
  • Xanthomatosis
  • Decreased HDL cholesterol concentration
  • Increased HDL cholesterol concentration

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

Hyperalphalipoproteinemia 1; Halp1 Is also known as cholesterol ester transfer protein deficiency, cetp deficiency.

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.

Hyperalphalipoproteinemia 1; Halp1 Recommended genes panels

Panel Name, Specifity and genes Tested/covered
High HDL.

By Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University (United States).

SCARB1, CETP
Specificity
50 %
Genes
100 %
CETP.

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

CETP
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 %
Comprehensive Cardiology Sequencing Panel with CNV Detection.

By PreventionGenetics PreventionGenetics (United States).

RYR1, RYR2, SCN1B, SCN2B, SCN4B, SCN5A, SCO2, SGCD, SGCG, BRAF, SLC25A4, SNTA1, SOS1, SREBF2, TAZ, TBX3, TBX5, TCAP, TGFB2, TGFB3 , (...)

View the complete list with 143 more genes
Specificity
1 %
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 %
CETP.

By Fulgent Genetics Fulgent Genetics (United States).

CETP
Specificity
100 %
Genes
100 %

You can get up to 1 more panels with our dedicated tool

Learn more

Sources and references

You can check the following sources for additional information.

OMIM ORPHANET Rare Disease Search Engine

If you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like PACHYDERMOPERIOSTOSIS GLOMUVENOUS MALFORMATIONS; GVM GLYCOGEN STORAGE DISEASE XII; GSD12 PSEUDOVAGINAL PERINEOSCROTAL HYPOSPADIAS; PPSH GRACILE BONE DYSPLASIA; GCLEB COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 15; COXPD15 AMELOGENESIS IMPERFECTA, TYPE IG; AI1G