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# Fredrickson classification of hyperlipoproteinaemias

The Fredrickson system sorts high blood fats into five types by which lipoprotein particle is raised. Each type points to typical causes and risks.

Updated 2026-11-01

## Key facts

- Type I: chylomicrons ↑ (LPL or ApoC-II deficiency); very high triglycerides, pancreatitis, eruptive xanthomas, lipaemia retinalis; little atherosclerosis.
- Type IIa: LDL ↑ (familial hypercholesterolaemia: LDL receptor, ApoB or PCSK9); tendon xanthomas and early coronary disease. Type IIb: LDL and VLDL ↑ (familial combined hyperlipidaemia).
- Type III: remnants/IDL ↑ (familial dysbetalipoproteinaemia, ApoE2/E2); cholesterol and triglycerides both high, palmar and tuberoeruptive xanthomas, 'broad β band'.
- Type IV: VLDL ↑ (familial hypertriglyceridaemia and secondary causes: obesity, diabetes, alcohol); the most common phenotype.
- Type V: VLDL and chylomicrons ↑; severe hypertriglyceridaemia with risk of acute pancreatitis.

## In detail

- 1. It is based on the pattern of lipoproteins seen by electrophoresis and ultracentrifugation (adopted by WHO in 1970), not on genes.
- 2. The same phenotype can come from different gene defects, and one family can show different types (for example IIa, IIb and IV in familial combined hyperlipidaemia).
- 3. Refrigerator test: a creamy top layer = chylomicrons (types I and V); a turbid whole sample = VLDL (types IV and V); clear plasma = LDL (type IIa).
- 4. Secondary causes must be ruled out first: diabetes, hypothyroidism, nephrotic syndrome, cholestasis, alcohol, obesity and drugs (corticosteroids, oestrogens, thiazides, some antiretrovirals, retinoids).
- 5. It does not include low HDL or high lipoprotein(a), so treatment decisions today rely on LDL cholesterol, triglycerides, apoB and total cardiovascular risk.
- 6. Triglycerides above about 1,000 mg/dL (11 mmol/L) carry a high risk of pancreatitis whatever the type.

## Memory aid

Type I = one particle (chylomicron); type IIb = IIa + IV (LDL + VLDL); type V = I + IV (chylomicrons + VLDL).

**Also called**
WHO/Fredrickson types I–V, Primary hyperlipoproteinaemias

## Clinical notes

- Tendon xanthomas suggest type IIa; palmar crease xanthomas suggest type III; eruptive xanthomas suggest types I or V.
- Hypothyroidism is a classic secondary cause of high LDL; it should be checked before starting lipid-lowering drugs.
- Types I and V are emergencies when triglycerides are very high, because of acute pancreatitis.

## Related conditions

- [Familial chylomicronemia syndrome (lipoprotein lipase deficiency)](https://durgical.com/en/conditions/familial-chylomicronemia-syndrome/)
- [Familial hypercholesterolemia](https://durgical.com/en/conditions/familial-hypercholesterolemia/)
- [Familial dysbetalipoproteinemia (type III hyperlipoproteinemia)](https://durgical.com/en/conditions/familial-dysbetalipoproteinemia/)
- [Familial combined hyperlipidaemia](https://durgical.com/en/conditions/familial-combined-hyperlipidaemia/)
- [Familial hypertriglyceridaemia](https://durgical.com/en/conditions/familial-hypertriglyceridaemia/)
- [Atherosclerosis and dyslipidaemia](https://durgical.com/en/conditions/atherosclerosis-and-dyslipidaemia/)
- [Acute pancreatitis](https://durgical.com/en/conditions/acute-pancreatitis/)
- [Hypothyroidism](https://durgical.com/en/conditions/hypothyroidism/)

## Related

- [Lipoprotein metabolism](https://durgical.com/en/biochemistry/topics/lipoprotein-metabolism/)
- [Chylomicron](https://durgical.com/en/biochemistry/topics/chylomicron/)
- [VLDL (very-low-density lipoprotein)](https://durgical.com/en/biochemistry/topics/vldl/)
- [LDL (low-density lipoprotein)](https://durgical.com/en/biochemistry/topics/ldl/)
- [HDL (high-density lipoprotein)](https://durgical.com/en/biochemistry/topics/hdl/)
- [Lipoprotein lipase (LPL)](https://durgical.com/en/biochemistry/enzymes/lipoprotein-lipase/)
- [LDL receptor](https://durgical.com/en/biochemistry/enzymes/ldl-receptor/)
- [Apolipoprotein E (ApoE)](https://durgical.com/en/biochemistry/enzymes/apolipoprotein-e/)
- [Apolipoprotein B (ApoB-100 and ApoB-48)](https://durgical.com/en/biochemistry/enzymes/apolipoprotein-b/)
- [PCSK9](https://durgical.com/en/biochemistry/enzymes/pcsk9/)
- [Centrifugation and ultracentrifugation](https://durgical.com/en/biochemistry/topics/centrifugation-and-ultracentrifugation/)
- [Plasma proteins and electrophoresis](https://durgical.com/en/biochemistry/topics/plasma-proteins-and-electrophoresis/)

## Test yourself

Think of the answer, then tap the question to see it.

## Which Fredrickson type is caused by lipoprotein lipase or ApoC-II deficiency?

Type I (raised chylomicrons), with very high triglycerides and risk of pancreatitis.

## Which lipoproteins are raised in type IIb?

LDL and VLDL, as in familial combined hyperlipidaemia.

## Which xanthoma suggests type III, and what genotype causes it?

Palmar crease xanthomas (xanthoma striata palmaris); usually ApoE2/E2 homozygosity with a second hit.

## What is the most common Fredrickson phenotype and what is raised?

Type IV, with raised VLDL, often worsened by obesity, diabetes or alcohol.

## What does a creamy layer on refrigerated plasma indicate?

Chylomicrons, as in types I and V.

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Educational information, not medical advice. For any symptom, see a health professional.

Sources: [Familial combined hyperlipidemia: MedlinePlus Medical Encyclopedia](https://medlineplus.gov/ency/article/000396.htm) (MedlinePlus, US National Library of Medicine, 2026); [Familial hypertriglyceridemia: MedlinePlus Medical Encyclopedia](https://medlineplus.gov/ency/article/000397.htm) (MedlinePlus, US National Library of Medicine, 2026); [Familial hypercholesterolemia: MedlinePlus Medical Encyclopedia](https://medlineplus.gov/ency/article/000392.htm) (MedlinePlus, US National Library of Medicine, 2026); [High blood cholesterol levels: MedlinePlus Medical Encyclopedia](https://medlineplus.gov/ency/article/000403.htm) (MedlinePlus, US National Library of Medicine, 2026); Textbook of Biochemistry for Medical Students, 6th ed. (Jaypee Brothers Medical Publishers (Vasudevan DM, Sreekumari S, Vaidyanathan K), 2011).

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