familial hypertriglyceridemia Gene Set

Dataset DISEASES Text-mining Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description A lipid metabolism disorder characterized by elevated triglyceride levels as a result of excess hepatic production of VLDL or heterozygous LPL deficiency. (Human Disease Ontology, DOID_0050527)
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23 genes co-occuring with the disease familial hypertriglyceridemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
LPL lipoprotein lipase 1.75414
USF1 upstream transcription factor 1 1.60681
APOB apolipoprotein B 1.46144
APOC3 apolipoprotein C-III 1.26996
SLC10A2 solute carrier family 10 (sodium/bile acid cotransporter), member 2 1.2356
GPD1 glycerol-3-phosphate dehydrogenase 1 (soluble) 1.13163
APOA2 apolipoprotein A-II 1.07866
APOA1 apolipoprotein A-I 1.03746
APOA5 apolipoprotein A-V 1.01301
APOE apolipoprotein E 0.893769
IGLV2-14 immunoglobulin lambda variable 2-14 0.888848
LPA lipoprotein, Lp(a) 0.862637
APOC2 apolipoprotein C-II 0.682693
INS insulin 0.645375
ABCG8 ATP-binding cassette, sub-family G (WHITE), member 8 0.560616
ABCG5 ATP-binding cassette, sub-family G (WHITE), member 5 0.549747
F13A1 coagulation factor XIII, A1 polypeptide 0.522273
SRI sorcin 0.480945
LMF1 lipase maturation factor 1 0.475634
SLC6A7 solute carrier family 6 (neurotransmitter transporter), member 7 0.46466
LIPI lipase, member I 0.434148
CETP cholesteryl ester transfer protein, plasma 0.317545
COG2 component of oligomeric golgi complex 2 0.317182