Heparin-induced Thrombocytopenia Pathway, Adverse Drug Reaction

No Pathway Network information available for Heparin-induced Thrombocytopenia Pathway, Adverse Drug Reaction

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

Disorders associated with Heparin-induced Thrombocytopenia Pathway, Adverse Drug Reaction SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Systemic lupus erythematosusEnrichmentBLK, FCGR2A, HLA-DRB1, IGHG1, IL107.21
2Bleeding disorder, platelet-type, 16EnrichmentITGA2B, ITGB34.66
3Recurrent infections associated with rare immunoglobulin isotypes deficiencyEnrichmentIGHG2, IGKC4.66
4Fetomaternal alloimmune thrombocytopenia 1EnrichmentITGA2B, ITGB33.97
5Glanzmann thrombasthenia 1EnrichmentITGA2B, ITGB33.82
6ThrombocytopeniaEnrichmentITGA2B, ITGB3, SRC3.53
7Autosomal dominant macrothrombocytopeniaEnrichmentITGA2B, ITGB33.49
8Precursor t-cell acute lymphoblastic leukemiaEnrichmentTRA, TRB2.75
9Prothrombin deficiency, congenitalEnrichmentF22.56
10Immunodeficiency 20EnrichmentFCGR3A2.56
11Fetomaternal alloimmune thrombocytopenia 2EnrichmentITGA2B2.56
12Okt4 epitope deficiencyEnrichmentCD42.56
13Graft-versus-host diseaseEnrichmentIL102.56
14Pulmonary alveolar proteinosis, acquiredEnrichmentHLA-DRB12.56
15Graham little-piccardi-lassueur syndromeEnrichmentHLA-DRA2.56
16Pregnancy loss, recurrent 2EnrichmentF22.56
17Immunodeficiency 22EnrichmentLCK2.56
18Thrombocytopenia 6EnrichmentSRC2.56
19Autoinflammatory disease, systemic, with vasculitisEnrichmentLYN2.56
20Immunodeficiency 79EnrichmentCD42.56
21Autoinflammation with pulmonary and cutaneous vasculitisEnrichmentHCK2.56
22Thrombocytopenia 10EnrichmentPTPRJ2.56
23Prothrombin deficiencyEnrichmentF22.56
24Immunoglobulin kappa light chain deficiencyEnrichmentIGKC2.26
25Maturity-onset diabetes of the young, type 11EnrichmentBLK2.26
26Sarcoidosis 1EnrichmentHLA-DRB12.26
27Trypsinogen deficiencyEnrichmentTRB2.26
28Bullous pemphigoidEnrichmentHLA-DRB12.26
29Pediatric multiple sclerosisEnrichmentHLA-DRB12.26
30Hyper-ige syndrome 1, autosomal dominant, with recurrent infectionsEnrichmentITGB32.09
31Immunodeficiency 7EnrichmentTRA2.09
32Bleeding disorder, platelet-type, 24EnrichmentITGB32.09
33Cerebral sinovenous thrombosisEnrichmentF22.09
34Vogt-koyanagi-harada diseaseEnrichmentHLA-DRB12.09
35Temporal arteritisEnrichmentHLA-DRB11.96
36Systemic-onset juvenile idiopathic arthritisEnrichmentHLA-DRB11.96
37Vitamin d-dependent rickets, type 2aEnrichmentTRB1.87
38Narcolepsy 2EnrichmentHLA-DRB11.87
39Glanzmann thrombasthenia 2EnrichmentITGB31.87
40Follicular lymphomaEnrichmentHLA-DRB11.87
41Diffuse cutaneous systemic sclerosisEnrichmentHLA-DRB11.87
42Limited sclerodermaEnrichmentHLA-DRB11.79
43Il10-related early-onset inflammatory bowel diseaseEnrichmentIL101.79
44Thrombophilia due to thrombin defectEnrichmentF21.72
45MyelofibrosisEnrichmentSRC1.72
46Narcolepsy 1EnrichmentHLA-DRB11.67
47Colorectal cancerEnrichmentPTPRJ, SRC1.63
48Rheumatoid arthritisEnrichmentIL101.61
49Leukemia, chronic lymphocyticEnrichmentIGHG11.57
50Stroke, ischemicEnrichmentF21.57
51Multiple sclerosisEnrichmentHLA-DRB11.43
52OsteoporosisEnrichmentSRC1.43
53Hereditary chronic pancreatitisEnrichmentTRB1.43
54Pancreatitis, hereditaryEnrichmentTRB1.34
55Human immunodeficiency virus type 1EnrichmentIL101.32
56Behcet syndromeEnrichmentIL101.30
57Maturity-onset diabetes of the youngEnrichmentBLK1.27
58Myocardial infarctionEnrichmentITGB31.23
59MalariaEnrichmentFCGR2A1.22
60Cystic fibrosisEnrichmentFCGR2A1.08
61Severe combined immunodeficiencyEnrichmentLCK1.06
62Cerebral palsyEnrichmentF20.99

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