Hyperlipoproteinemia, type 1D

MONDO:0014412

Any familial hyperlipidemia in which the cause of the disease is a mutation in the GPIHBP1 gene.

Also known as: GPIHBP1 familial hyperlipidemia, familial hyperlipidemia caused by mutation in GPIHBP1, hyperlipoproteinemia, type 1D, hyperlipoproteinemia, type ID

1 clinical trial for this condition and its sub-types, 0 tagged with Hyperlipoproteinemia, type 1D itself.

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Where it sits in the disease tree

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↑ Autosomal recessive disease (994) ↑ Familial hyperlipidemia (130) ↑ Syndromic dyslipidemia (73) ↑ Familial chylomicronemia syndrome (13)

Including sub-types (1) Tagged with Hyperlipoproteinemia, type 1D (0)

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