Sunitinib Pathway, Pharmacokinetics/Pharmacodynamics

Pathway network for the Sunitinib Pathway, Pharmacokinetics/Pharmacodynamics SuperPath

Sources:
  • PharmGKB

Gene overlap in member pathways for Sunitinib Pathway, Pharmacokinetics/Pharmacodynamics SuperPath

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

Disorders associated with Sunitinib Pathway, Pharmacokinetics/Pharmacodynamics SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Hyperbilirubinemia, rotor typeEnrichmentSLCO1B1, SLCO1B35.25
2Acute myeloid leukemia with abnormal bone marrow eosinophils inv(16)(p13q22) or t(16;16)(p13;q22)EnrichmentFLT3, KIT5.16
3Acute myeloid leukemia with maturationEnrichmentFLT3, KIT4.94
4Acute myeloid leukemia with t(8;21)(q22;q22) translocationEnrichmentFLT3, KIT4.94
5Primary hypereosinophilic syndromeEnrichmentPDGFRA, PDGFRB4.94
6Hemangioma, capillary infantileEnrichmentFLT4, KDR4.77
7Gastrointestinal stromal tumorEnrichmentKIT, PDGFRA4.62
8Gilbert syndromeEnrichmentSLCO1B1, UGT1A13.99
9Acute myeloid leukemia with minimal differentiationEnrichmentFLT33.66
10Vitamin d-dependent rickets, type 3EnrichmentCYP3A43.66
11Tetralogy of fallotEnrichmentFLT4, KDR3.44
12Acute myeloid leukemia without maturationEnrichmentFLT33.35
13Mixed phenotype acute leukemia with t(9;22)(q34.1;q11.2)EnrichmentFLT33.35
14Mixed phenotype acute leukemia with tEnrichmentFLT33.18
15Leukemia, acute myeloidEnrichmentFLT3, KIT3.06
16Chronic myelomonocytic leukemiaEnrichmentFLT33.05
17Premature aging syndrome, penttinen typeEnrichmentPDGFRB2.96
18Hypereosinophilic syndrome, idiopathicEnrichmentPDGFRA2.96
19Mastocytosis, cutaneousEnrichmentKIT2.96
20Colchicine resistanceEnrichmentABCB12.96
21Uric acid concentration, serum, quantitative trait locus 1EnrichmentABCG22.96
22Myofibromatosis, infantile, 1EnrichmentPDGFRB2.96
23Gist-plus syndromeEnrichmentPDGFRA2.96
24Encephalopathy, acute transientEnrichmentABCB12.96
25Myeloid and lymphoid neoplasms associated with pdgfra rearrangementEnrichmentPDGFRA2.96
26Inflammatory bowel disease 13EnrichmentABCB12.96
27Basal ganglia calcification, idiopathic, 4EnrichmentPDGFRB2.96
28Myeloid and lymphoid neoplasms associated with pdgfrb rearrangementEnrichmentPDGFRB2.96
29Kosaki overgrowth syndromeEnrichmentPDGFRB2.96
30Blood group, junior systemEnrichmentABCG22.96
31Congenital heart defects, multiple types, 7EnrichmentFLT42.96
32Ocular pterygium-digital keloid dysplasia syndromeEnrichmentPDGFRB2.96
33Chronic mast cell leukemiaEnrichmentKIT2.96
34Tufted angioma of skinEnrichmentKDR2.96
35Isolated bone marrow mastocytosisEnrichmentKIT2.96
36Smoldering systemic mastocytosisEnrichmentKIT2.96
37MastocytosisEnrichmentKIT2.96
38Cutaneous mastocytomaEnrichmentKIT2.96
39Typical urticaria pigmentosaEnrichmentKIT2.96
40Nodular urticaria pigmentosaEnrichmentKIT2.96
41Pseudoxanthomatous diffuse cutaneous mastocytosisEnrichmentKIT2.96
42Telangiectasia macularis eruptiva perstansEnrichmentKIT2.96
43Acute mast cell leukemiaEnrichmentKIT2.96
44Plaque-form urticaria pigmentosaEnrichmentKIT2.96
45Bullous diffuse cutaneous mastocytosisEnrichmentKIT2.96
46Testis seminomaEnrichmentKIT2.96
47Drug metabolism, poor, cyp2c19-relatedEnrichmentCYP2C192.85
48Drug metabolism, poor, cyp2d6-relatedEnrichmentCYP2D62.85
49B-lymphoblastic leukemia/lymphoma with t(9;22)(q34.1;q11.2)EnrichmentFLT32.81
50Atypical chronic myeloid leukemia, bcr-abl1 negativeEnrichmentFLT32.70
51Lymphatic malformation 1EnrichmentFLT42.66
52Myeloproliferative disorder, chronic, with eosinophiliaEnrichmentPDGFRB2.66
53Intracranial hypertension, idiopathicEnrichmentFLT42.66
54Piebald traitEnrichmentKIT2.66
55Angioma, tuftedEnrichmentKDR2.66
56Infantile myofibromatosisEnrichmentPDGFRB2.66
57Hereditary lymphedema iEnrichmentFLT42.66
58Chronic eosinophilic leukemiaEnrichmentPDGFRA2.66
59B-lymphoblastic leukemia/lymphoma with recurrent genetic abnormalityEnrichmentPDGFRA2.66
60B-lymphoblastic leukemia/lymphoma with tEnrichmentKIT2.66
61Leukemia, acute lymphoblasticEnrichmentFLT32.61
62Testicular germ cell cancerEnrichmentKIT2.48
63Hypertension, essentialEnrichmentCYP3A52.43
64Coumarin resistanceEnrichmentCYP2C92.38
65Systemic mastocytosis with associated hematologic neoplasmEnrichmentKIT2.35
66Precursor t-cell acute lymphoblastic leukemiaEnrichmentFLT32.29
67Ovarian cancerEnrichmentKIT, PDGFRA2.27
68Pre-eclampsiaEnrichmentFLT12.26
69Testicular germ cell tumorEnrichmentKIT2.18
70Basal ganglia calcification, idiopathic, 1EnrichmentPDGFRB2.05
71Inherited cancer-predisposing syndromeEnrichmentKIT, PDGFRA2.04
72Epilepsy, idiopathic generalizedEnrichmentABCB11.92
73Myeloma, multipleEnrichmentFLT31.91
74Lip and oral cavity carcinomaEnrichmentKIT1.88
75Crigler-najjar syndrome, type iEnrichmentUGT1A11.86
76Hyperbilirubinemia, transient familial neonatalEnrichmentUGT1A11.86
77Bilirubin, serum level of, quantitative trait locus 1EnrichmentUGT1A11.86
78Crigler-najjar syndrome, type iiEnrichmentUGT1A11.86
79Bilirubin metabolic disorderEnrichmentUGT1A11.82
80Cleft lip/palateEnrichmentPDGFRA1.81
81HydrocephalusEnrichmentPDGFRB1.78
82Dandy-walker syndromeEnrichmentPDGFRB1.73
83Hydrops fetalis, nonimmuneEnrichmentFLT41.55
84Non-immune hydrops fetalisEnrichmentFLT41.47
85Cerebral palsyEnrichmentPDGFRB1.37
86Primary ovarian insufficiencyEnrichmentKDR1.20

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