familial lipoprotein lipase deficiency Gene Set

Dataset DISEASES Text-mining Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description OMIM mapping confirmed by DO. [SN]. (Human Disease Ontology, DOID_14118)
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28 genes co-occuring with the disease familial lipoprotein lipase deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
LPL lipoprotein lipase 2.59677
APOC2 apolipoprotein C-II 2.05
GPIHBP1 glycosylphosphatidylinositol anchored high density lipoprotein binding protein 1 1.74005
APOA5 apolipoprotein A-V 1.6171
LMF1 lipase maturation factor 1 1.21868
PNLIP pancreatic lipase 1.18281
LIPC lipase, hepatic 1.11309
INTS8 integrator complex subunit 8 1.09545
APOB apolipoprotein B 0.81018
AMT aminomethyltransferase 0.776568
APOA2 apolipoprotein A-II 0.552851
LCAT lecithin-cholesterol acyltransferase 0.54393
MYDGF myeloid-derived growth factor 0.538118
SACS sacsin molecular chaperone 0.521502
APOD apolipoprotein D 0.502675
APOE apolipoprotein E 0.501909
APOA1 apolipoprotein A-I 0.396725
ANOS1 anosmin 1 0.362239
USF1 upstream transcription factor 1 0.337975
CYP27B1 cytochrome P450, family 27, subfamily B, polypeptide 1 0.290821
PABPN1 poly(A) binding protein, nuclear 1 0.275089
LPA lipoprotein, Lp(a) 0.256652
HBD hemoglobin, delta 0.219398
SCN2A sodium channel, voltage gated, type II alpha subunit 0.212608
F12 coagulation factor XII (Hageman factor) 0.206248
DLL1 delta-like 1 (Drosophila) 0.196779
HEXA hexosaminidase A (alpha polypeptide) 0.188632
APOC3 apolipoprotein C-III 0.187719