Familial hyperlipidemia

MONDO:0001336

An instance of hyperlipidemia (disease) that is caused by an inherited modification of the individual's genome.

Also known as: hyperlipemia, hyperlipidaemia, hereditary hyperlipidemia (disease), familial hyperlipemia, familial hyperlipoproteinemia

131 clinical trials for this condition and its sub-types, 8 tagged with Familial hyperlipidemia itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →
Sort by