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Severe hypertriglyceridaemia (Version 1.18)

Level 3: Arteriopathies
Level 2: Cardiovascular disorders

Panel types: Rare Disease 100K
Previous code: 57eab3658f620356ef5e4010
Description
This panel is NO LONGER ACTIVELY MAINTAINED.

Please use with caution, as the gene list has not been recently updated. Reviews added to this panel are no longer a priority for curation and may not be followed up.

Please consider using an NHS Genomic Medicine Service (GMS) panel instead. The full list of GMS panels can be found here: https://nhsgms-panelapp.genomicsengland.co.uk/panels, with links back to PanelApp should you wish to leave a review on the panel.

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Eligibility statement for Severe hypertriglyceridaemia:

Severe hypertriglyceridaemia inclusion criteria (42186)
Triglycerides >20mmol/L 
AND one of 
Asymptomatic, OR
Acute pancreatitis event, OR
Eruptive xanthomata

Individuals with severe or syndromic disease should be recruited according to standard guidance, typically as trios. Disease status of apparently unaffected participants should be determined according to standard clinical practice to detect cryptic disease.

In other cases, unaffected individuals should not be recruited. Recruitment in such families should favour multiplex families over single isolated cases. These singleton recruits will not contribute to the overall singleton monitoring metrics applied to GMCs.

Severe hypertriglyceridaemia exclusion criteria (42186)
Excess alcohol intake ( >30 units/week) 
Uncontrolled diabetes ( HbA1c >8%) 
Known lipodystrophy syndrome- genetic or acquired 
Known mitochondrial myopathy 
Use of anti-retroviral drug therapies

Prior genetic testing guidance (42186)
- Results should have been reviewed for all genetic tests undertaken, including disease-relevant genes in exome sequencing data. The patient is not eligible if they have a molecular diagnosis for their condition. 
- Genetic testing should continue according to routine local practice for this phenotype regardless of recruitment to the project; results of these tests must be submitted via the ‘Genetic investigations’ section of the data capture tool to allow comparison of WGS with current standard testing.  

PLEASE NOTE: The sensitivity of WGS compared to current diagnostic genetic testing has not yet been established. It is therefore important that tests which are clinically indicated under local standard practice continue to be carried out.

Severe hypertriglyceridaemia prior genetic testing genes (42186)
Testing of the following genes should be carried out PRIOR TO RECRUITMENT where this is in line with current local practice: 
LPL, APOA5, APOC2, GPIHBP1, LMF1

Closing statement (42186)
These requirements will be kept under continual review during the main programme and may be subject to change.
Panel Activity

3 reviewers

  • Ellen McDonagh (Genomics England Curator)

    Group: Other
    Workplace: Other

  • steve Humphries (UCL)

    Group: GeCIP domain
    Workplace: Research lab

  • Sarah Leigh (Genomics England Curator)

    Group: Other
    Workplace: Other

8 Entities

8 reviewed, 7 green

List Entity Reviews Mode of inheritance Details
8 Entitiess
Green List (high evidence)
APOA5
3 reviews
2 green
BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal
Sources
  • Eligibility statement prior genetic testing
  • Expert Review Green
  • Radboud University Medical Center, Nijmegen
  • UKGTN
Phenotypes
  • Hyperchylomicronemia, late-onset OMIM:144650
  • hyperlipoproteinemia type V MONDO:0007762
  • {Hypertriglyceridemia, susceptibility to} OMIM:145750
  • hypertriglyceridemia, familial MONDO:0007788
Tags
Green List (high evidence)
APOC2
3 reviews
1 green
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Eligibility statement prior genetic testing
  • Expert Review Green
  • UKGTN
Phenotypes
  • Hyperlipoproteinemia, type Ib 207750
Tags
Green List (high evidence)
CREB3L3
1 review
1 green
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Hypertriglyceridemia 2, OMIM:619324
Tags
Green List (high evidence)
GPD1
3 reviews
1 green
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Radboud University Medical Center, Nijmegen
Phenotypes
  • Hypertriglyceridemia, transient infantile, 614480
Tags
Green List (high evidence)
GPIHBP1
3 reviews
1 green
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Eligibility statement prior genetic testing
  • Expert Review Green
  • UKGTN
Phenotypes
  • Hyperlipoproteinemia, type 1D, 615947
Tags
Green List (high evidence)
LMF1
3 reviews
1 green
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Eligibility statement prior genetic testing
  • Expert Review Green
  • UKGTN
Phenotypes
  • Lipase deficiency, combined, 246650
Tags
Green List (high evidence)
LPL
3 reviews
1 green
BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Sources
  • Eligibility statement prior genetic testing
  • Expert Review Green
  • Illumina TruGenome Clinical Sequencing Services
  • Radboud University Medical Center, Nijmegen
  • UKGTN
Phenotypes
  • Combined hyperlipidemia, familial 144250
  • Lipoprotein lipase deficiency, 238600
Tags
Red List (low evidence)
CELSR2
1 review
1 red
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Other
Phenotypes
  • hypertriglyceridaemia
Tags

Major version comments

  • Review added and all genes checked

Downloads

Download lists

  • Whole panel
  • Green list (high evidence)
  • Green and Amber Genes
  • Amber Genes
  • Red list (low evidence)

Download Version