- OMIM ID
-
238600
- OMIM term:
- HYPERLIPOPROTEINEMIA, TYPE I
- Alternative terms:
-
LIPOPROTEIN LIPASE DEFICIENCY
LPL DEFICIENCY
HYPERCHYLOMICRONEMIA, FAMILIAL
HYPERLIPEMIA, IDIOPATHIC, BURGER-GRUTZ TYPE
HYPERLIPEMIA, ESSENTIAL FAMILIAL
LIPASE D DEFICIENCY
LIPD DEFICIENCY
HYPERLIPOPROTEINEMIA, TYPE IA
CHYLOMICRONEMIA, FAMILIAL
- (∗) Location:
- 8p21.3
- (†) Associated OMIM genes:
- LPL HIGH DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 11, INCLUDED; HDLCQ11, INCLUDED
- (‡) Associated MGI genes:
- Lpl
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