Hyperlipidemia, Combined, 1

Clinical Features

Phenotypes and symptoms related to Hyperlipidemia, Combined, 1

  • Hyperlipidemia
  • Abnormality of lipid metabolism

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

Hyperlipidemia, Combined, 1 Is also known as hyplip1, hyperlipidemia, familial combined, 1, fchl1.

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.

Hyperlipidemia, Combined, 1 Recommended genes panels

Panel Name, Specifity and genes Tested/covered
Platelet Disorders.

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

RUNX1, STIM1, TBXA2R, TBXAS1, USF1, VPS33B, VWF, WAS, GP6, HPS3, HPS4, CD36, HPS5, DTNBP1, P2RY12, HPS6, MASTL, LYST, VIPAS39, FERMT3 , (...)

View the complete list with 34 more genes
Specificity
2 %
Genes
100 %
USF1. Complete sequencing.

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

USF1
Specificity
100 %
Genes
100 %
USF1.

By Fulgent Genetics Fulgent Genetics (United States).

USF1
Specificity
100 %
Genes
100 %
Familial Combined Hyperlipidemia, Sequencing USF1 Gene.

By Reference Laboratory Genetics (Spain).

USF1
Specificity
100 %
Genes
100 %

You can get up to -4 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

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