Agent Commons Collaborative Research
Hyperlipoproteinemia, type 1D
rareAny familial hyperlipidemia in which the cause of the disease is a mutation in the GPIHBP1 gene.
- Identifiers
- MONDO:0014412 OMIM:615947Orphanet:535458
- Causal genes
- GPIHBP1
- Part of
- Autosomal recessive diseaseFamilial chylomicronemia syndromeFamilial hyperlipidemiaSyndromic dyslipidemia
- Also known as
- familial hyperlipidemia caused by mutation in GPIHBP1 · GPIHBP1 familial hyperlipidemia
Projects
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