Statin inhibition of cholesterol production

Pathway network for the Statin inhibition of cholesterol production SuperPath

Sources:
  • WikiPathways
  • PharmGKB

Ordered by rank within the SuperPath, via the multiplicity of each gene in the constituent pathways

Disorders associated with Statin inhibition of cholesterol production SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Lipid metabolism disorderEnrichmentABCG5, ABCG8, APOE, LDLR, LIPC10.71
2Coronary heart disease 5EnrichmentABCA1, ABCG5, ABCG8, APOB, LDLR10.66
3Familial hypercholesterolemiaEnrichmentAPOA2, APOB, APOE, LDLR9.67
4Homozygous familial hypercholesterolemiaEnrichmentABCG5, ABCG8, APOB, LDLR9.19
5Hyperlipidemia, familial combined, 3EnrichmentAPOB, LDLR, LPL8.54
6Hyperalphalipoproteinemia 1EnrichmentAPOC3, CETP, SCARB18.10
7Hypercholesterolemia, familial, 1EnrichmentAPOA2, APOB, LDLR7.09
8Hyperlipoproteinemia, type iiiEnrichmentAPOE, LDLR6.31
9Hypercholesterolemia, familial, 2EnrichmentAPOB, LDLR5.83
10Coronary artery anomalyEnrichmentAPOC3, LPL5.53
11Gallbladder disease 4EnrichmentABCG5, ABCG85.49
12Sitosterolemia 1EnrichmentABCG5, ABCG85.01
13SitosterolemiaEnrichmentABCG5, ABCG85.01
14Hypoalphalipoproteinemia, primary, 2EnrichmentABCA1, APOA14.91
15Hypoalphalipoproteinemia, primary, 1EnrichmentABCA1, APOA14.61
16Sea-blue histiocyte diseaseEnrichmentAPOE3.13
17Lipoprotein glomerulopathyEnrichmentAPOE3.13
18Apolipoprotein c-iii deficiencyEnrichmentAPOC33.13
19Aapoaii amyloidosisEnrichmentAPOA23.13
20Atrophoderma vermiculataEnrichmentLRP13.02
21High density lipoprotein cholesterol level quantitative trait locus 6EnrichmentSCARB13.02
22Keratosis pilaris atrophicansEnrichmentLRP13.02
23Hepatic lipase deficiencyEnrichmentLIPC3.02
24High density lipoprotein cholesterol level quantitative trait locus 12EnrichmentLIPC3.02
25Tubulointerstitial kidney disease, autosomal dominant 6EnrichmentAPOA43.02
26Cerebellar hypoplasiaEnrichmentVLDLR3.02
27Hyperlipidemia due to hepatic triglyceride lipase deficiencyEnrichmentLIPC3.02
28Fish-eye diseaseEnrichmentLCAT2.83
29Apolipoprotein c-ii deficiencyEnrichmentAPOC22.83
30Hyperlipoproteinemia, type iEnrichmentLPL2.83
31Lecithin:cholesterol acyltransferase deficiencyEnrichmentLCAT2.83
32Alzheimer disease 3EnrichmentAPOE2.83
33Lipase deficiency, combinedEnrichmentLPL2.83
34Hypobetalipoproteinemia, familial, 1EnrichmentAPOB2.83
35Familial apolipoprotein c-ii deficiencyEnrichmentAPOC22.83
36HypobetalipoproteinemiaEnrichmentAPOB2.83
37Familial lipoprotein lipase deficiencyEnrichmentLPL2.83
38Hypoalphalipoproteinemia, primary, 2, intermediateEnrichmentAPOA12.83
39Amyloidosis, hereditary systemic 3EnrichmentAPOA12.83
40AbetalipoproteinemiaEnrichmentMTTP2.73
41Colchicine resistanceEnrichmentABCB12.73
42Encephalopathy, acute transientEnrichmentABCB12.73
43Familial apolipoprotein a5 deficiencyEnrichmentAPOA52.73
44Inflammatory bowel disease 13EnrichmentABCB12.73
45Hypercholesterolemia due to cholesterol 7alpha-hydroxylase deficiencyEnrichmentCYP7A12.73
46Low density lipoprotein cholesterol level quantitative trait locus 3EnrichmentHMGCR2.73
47Muscular dystrophy, limb-girdle, autosomal recessive 28EnrichmentHMGCR2.73
48Developmental dysplasia of the hip 3EnrichmentLRP12.72
49Cerebellar ataxia, impaired intellectual development, and dysequilibrium syndromeEnrichmentVLDLR2.72
50HypoalphalipoproteinemiaEnrichmentABCA12.69
51Intellectual developmental disorder with microcephaly and pontine and cerebellar hypoplasiaEnrichmentLDLR2.66
52Alzheimer disease 4EnrichmentAPOE2.66
53Hypercholesterolemia, familial, 4EnrichmentLDLR2.66
54Syndromic x-linked intellectual disability najm typeEnrichmentLDLR2.66
55Spastic paraplegia 50, autosomal recessiveEnrichmentAPOA12.66
56Keratosis follicularis spinulosa decalvansEnrichmentLRP12.54
57Macular degeneration, age-related, 1EnrichmentAPOE2.53
58Alzheimer disease 2EnrichmentAPOE2.43
59Amyloidosis, hereditary systemic 2EnrichmentAPOA12.43
60Hyperlipoproteinemia, type vEnrichmentAPOA52.43
61Abdominal obesity-metabolic syndrome 1EnrichmentMTTP2.43
62Sitosterolemia 2EnrichmentABCG52.43
63Squalene synthase deficiencyEnrichmentFDFT12.43
64Short-rib thoracic dysplasia 15 with polydactylyEnrichmentABCG52.43
65Tangier diseaseEnrichmentABCA12.38
66Cowden syndrome 1EnrichmentLDLR2.35
67Cerebellar ataxia, impaired intellectual development, and dysequilibrium syndrome 1EnrichmentVLDLR2.24
68Hypertriglyceridemia 1EnrichmentAPOA52.13
69Diarrhea 7, protein-losing enteropathy typeEnrichmentDGAT12.13
70Congenital diarrhea 7 with exudative enteropathyEnrichmentDGAT12.04
71Alzheimer's diseaseEnrichmentAPOE2.02
72DiarrheaEnrichmentDGAT11.96
73Alzheimer disease, familial, 1EnrichmentAPOE1.90
74Cardiomyopathy, dilated, 1aEnrichmentLPL1.81
75Limb-girdle muscular dystrophyEnrichmentHMGCR1.78
76Epilepsy, idiopathic generalizedEnrichmentABCB11.70
77Type 2 diabetes mellitusEnrichmentLIPC1.40
78Short-rib thoracic dysplasia 1 with or without polydactylyEnrichmentABCG51.23
79Congenital nervous system abnormalityEnrichmentVLDLR1.01
80Nervous system diseaseEnrichmentVLDLR1.01
81Breast cancerEnrichmentABCA10.84

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