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Dictionary » Familial hyperlipoproteinemia type IV
 

Familial hyperlipoproteinemia type IV

Introduction: Familial hyperlipoproteinemia type IV

Description of Familial hyperlipoproteinemia type IV

Familial hyperlipoproteinemia type IV: characterized by an isolated elevation in the plasma level of endogenously synthesized triglyceride carried in VLDL; considered to be an autosomal dominant trait.
Source: CRISP

Familial hyperlipoproteinemia type IV: Related Topics

These medical condition or symptom topics may be relevant to medical information for Familial hyperlipoproteinemia type IV:

Familial hyperlipoproteinemia type IV: Rare Disease

Office of Rare Diseases (ORD) of the National Institutes of Health (NIH)

Familial hyperlipoproteinemia type IV is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Familial hyperlipoproteinemia type IV, or a subtype of Familial hyperlipoproteinemia type IV, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

Terms associated with Familial hyperlipoproteinemia type IV:

Terms Similar to Familial hyperlipoproteinemia type IV:

Source - NIH

Broader terms for Familial hyperlipoproteinemia type IV

Source - CRISP

The term Familial hyperlipoproteinemia type IV can be used for:

Source: CRISP

Other terms that may be related to Familial hyperlipoproteinemia type IV:

Source: CRISP

The description of Familial hyperlipoproteinemia type IV may also be used for the following terms:

Source: CRISP

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