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MIM:238600 - HYPERLIPOPROTEINEMIA, TYPE I
Xenbase Genes: lpl
Human Disease Resource: MIM
| MONDO:0009387 - familial lipoprotein lipase deficiency |
| MONDO:0018637 - familial chylomicronemia syndrome |
| DOID:14118 - familial lipoprotein lipase deficiency |
|
| MONDO:0009387 - familial lipoprotein lipase deficiency |
| MONDO:0018637 - familial chylomicronemia syndrome |
| DOID:14118 - familial lipoprotein lipase deficiency |