Erlotinib Pathway, Pharmacokinetics

Pathway network for the Erlotinib Pathway, Pharmacokinetics SuperPath

Sources:
  • PharmGKB

Gene overlap in member pathways for Erlotinib Pathway, Pharmacokinetics SuperPath

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

Disorders associated with Erlotinib Pathway, Pharmacokinetics SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Crigler-najjar syndrome, type iEnrichmentUGT1A1, UGT1A7, UGT1A97.20
2Hyperbilirubinemia, transient familial neonatalEnrichmentUGT1A1, UGT1A7, UGT1A97.20
3Bilirubin, serum level of, quantitative trait locus 1EnrichmentUGT1A1, UGT1A7, UGT1A97.20
4Crigler-najjar syndrome, type iiEnrichmentUGT1A1, UGT1A7, UGT1A97.20
5Gilbert syndromeEnrichmentUGT1A1, UGT1A7, UGT1A97.06
6Bilirubin metabolic disorderEnrichmentUGT1A1, UGT1A7, UGT1A97.06
7Colchicine resistanceEnrichmentABCB13.23
8Uric acid concentration, serum, quantitative trait locus 1EnrichmentABCG23.23
9Encephalopathy, acute transientEnrichmentABCB13.23
10Inflammatory bowel disease 13EnrichmentABCB13.23
11Blood group, junior systemEnrichmentABCG23.23
12Vitamin d-dependent rickets, type 3EnrichmentCYP3A43.23
13Drug metabolism, poor, cyp2d6-relatedEnrichmentCYP2D63.05
14Severe primary trimethylaminuriaEnrichmentFMO33.05
15Neonatal nephrocutaneous inflammatory syndromeEnrichmentEGFR2.75
16Neonatal inflammatory skin and bowel diseaseEnrichmentEGFR2.75
17Glaucoma 1, open angle, aEnrichmentCYP1B12.75
18Anterior segment dysgenesis 6EnrichmentCYP1B12.75
19TrimethylaminuriaEnrichmentFMO32.75
20Primary trimethylaminuriaEnrichmentFMO32.75
21Primary congenital glaucomaEnrichmentCYP1B12.75
22Coumarin resistanceEnrichmentCYP2C92.58
23Cowden syndrome 1EnrichmentEGFR2.45
24Lung squamous cell carcinomaEnrichmentEGFR2.45
25Glaucoma 3, primary infantile, bEnrichmentCYP1B12.45
26Squamous cell carcinoma, head and neckEnrichmentEGFR2.38
27Juvenile glaucomaEnrichmentCYP1B12.35
28Glaucoma, primary open angleEnrichmentCYP1B12.28
29Anterior segment dysgenesis 5EnrichmentCYP1B12.28
30Glaucoma 3, primary congenital, aEnrichmentCYP1B12.21
31Epilepsy, idiopathic generalizedEnrichmentABCB12.19
32Lung non-small cell carcinomaEnrichmentEGFR2.19
33Lip and oral cavity carcinomaEnrichmentEGFR2.15
34Lung cancer susceptibility 3EnrichmentEGFR2.08
35Peters-plus syndromeEnrichmentCYP1B12.05
36GliosarcomaEnrichmentEGFR2.03
37Hypertension, essentialEnrichmentCYP3A52.00
38Giant cell glioblastomaEnrichmentEGFR2.00
39Arteriovenous malformations of the brainEnrichmentEGFR1.95
40Anterior segment dysgenesisEnrichmentCYP1B11.88
41Bladder cancerEnrichmentEGFR1.77
42Lung cancerEnrichmentEGFR1.73
43Ovarian cancerEnrichmentEGFR1.24
44Inherited cancer-predisposing syndromeEnrichmentEGFR1.12

Loading...
Loading...
Loading...