Th2 Differentiation

No Pathway Network information available for Th2 Differentiation

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

Disorders associated with Th2 Differentiation SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Oligoarticular juvenile idiopathic arthritisEnrichmentIL2RA, IL2RB, STAT45.90
2Rheumatoid factor-negative juvenile idiopathic arthritisEnrichmentIL2RA, IL2RB, STAT45.90
3Human immunodeficiency virus type 1EnrichmentCCL11, IFNG, IL104.54
4Breast implant-associated anaplastic large cell lymphomaEnrichmentJAK1, JAK24.47
5Adams-oliver syndromeEnrichmentNOTCH1, RBPJ3.63
6Systemic lupus erythematosusEnrichmentIL10, STAT4, TNFSF43.51
7AsthmaEnrichmentCCL11, IL133.22
8Behcet syndromeEnrichmentIL10, STAT42.73
9Type 1 diabetes mellitus 10EnrichmentIL2RA2.47
10Immunodysregulation, polyendocrinopathy, and enteropathy, x-linkedEnrichmentFOXP32.47
11Cataract 21, multiple typesEnrichmentMAF2.47
12Short sleep, familial natural, 1EnrichmentBHLHE412.47
13Immunodeficiency 16EnrichmentTNFRSF42.47
14Charcot-marie-tooth disease, axonal, type 2hhEnrichmentJAG12.47
15Immunodeficiency 69EnrichmentIFNG2.47
16Hyper-ige syndrome 6, autosomal dominant, with recurrent infectionsEnrichmentSTAT62.47
17Immunodeficiency 63 with lymphoproliferation and autoimmunityEnrichmentIL2RB2.47
18Disabling pansclerotic morphea of childhoodEnrichmentSTAT42.47
19Okt4 epitope deficiencyEnrichmentCD42.47
20Graft-versus-host diseaseEnrichmentIL102.47
21Immunodeficiency 18EnrichmentCD3E2.47
22Systemic lupus erythematosus 11EnrichmentSTAT42.47
23Ayme-gripp syndromeEnrichmentMAF2.47
24Allergic rhinitisEnrichmentIL132.47
25Graham little-piccardi-lassueur syndromeEnrichmentHLA-DRA2.47
26Immunodeficiency 123 with hpv-related verrucosisEnrichmentCD282.47
27Muscular dystrophy, limb-girdle, autosomal recessive 27EnrichmentJAG22.47
28Deafness, congenital heart defects, and posterior embryotoxonEnrichmentJAG12.47
29Immunodeficiency 79EnrichmentCD42.47
30T-b+ severe combined immunodeficiency due to jak3 deficiencyEnrichmentJAK32.47
31Mendelian susceptibility to mycobacterial diseases due to partial jak1 deficiencyEnrichmentJAK12.47
32Tetralogy of fallotEnrichmentJAG1, NOTCH12.46
33Severe combined immunodeficiencyEnrichmentCD3E, JAK32.26
34Hypoparathyroidism, sensorineural deafness, and renal dysplasia syndromeEnrichmentGATA32.17
35Multinucleated neurons, anhydramnios, renal dysplasia, cerebellar hypoplasia, and hydranencephalyEnrichmentFOXP32.17
36Hemangiopericytoma, malignantEnrichmentSTAT62.17
37Immunodeficiency 41 with lymphoproliferation and autoimmunityEnrichmentIL2RA2.17
38Neutropenia, nonimmune chronic idiopathic, of adultsEnrichmentGFI12.17
39Developmental and epileptic encephalopathy 28EnrichmentMAF2.17
40Adams-oliver syndrome 5EnrichmentNOTCH12.17
41Neutropenia, severe congenital, 2, autosomal dominantEnrichmentGFI12.17
42Thrombocythemia 3EnrichmentJAK22.17
43Spinocerebellar ataxia, autosomal recessive 12EnrichmentMAF2.17
44Adams-oliver syndrome 3EnrichmentRBPJ2.17
45Autoinflammation, immune dysregulation, and eosinophiliaEnrichmentJAK12.17
46B-lymphoblastic leukemia/lymphoma with hyperdiploidyEnrichmentGATA32.17
47Hypoparathyroidism-deafness-renal disease syndromeEnrichmentGATA32.17
48PolycythemiaEnrichmentJAK22.17
49Autosomal dominant nonsyndromic deafnessEnrichmentGATA32.17
50Hypereosinophilic syndromeEnrichmentJAK22.17
51Severe combined immunodeficiency, autosomal recessive, t cell-negative, b cell-negative, nk cell-negative, due to adenosine deaminase deficiencyEnrichmentJAK31.99
52Alagille syndrome 1EnrichmentJAG11.99
53Polycythemia veraEnrichmentJAK21.99
54Mycosis fungoidesEnrichmentCD281.99
55Tuberous sclerosis 1EnrichmentIFNG1.99
56Severe combined immunodeficiency, x-linkedEnrichmentIL2RG1.99
57Combined immunodeficiency, x-linkedEnrichmentIL2RG1.99
58Hepatitis c virusEnrichmentIFNG1.99
59Tuberous sclerosis 2EnrichmentIFNG1.99
60End stage renal diseaseEnrichmentGATA31.99
61T-b+ severe combined immunodeficiency due to cd3delta/cd3epsilon/cd3zetaEnrichmentCD3E1.99
62KeratoacanthomaEnrichmentNOTCH11.99
63Saczary syndromeEnrichmentCD281.99
64Erythrocytosis, familial, 1EnrichmentJAK21.87
65Budd-chiari syndromeEnrichmentJAK21.87
66Adenosine deaminase deficiencyEnrichmentJAK31.87
67Congenital blue dot cataractEnrichmentMAF1.87
68Pediatric systemic lupus erythematosusEnrichmentSTAT41.87
69Middle aortic syndromeEnrichmentJAG11.87
70Severe combined immunodeficiency, autosomal recessive, t cell-negative, b cell-positive, nk cell-negativeEnrichmentJAK31.77
71Myeloproliferative neoplasmEnrichmentJAK21.77
72Autosomal dominant severe congenital neutropeniaEnrichmentGFI11.77
73Idiopathic aplastic anemiaEnrichmentIFNG1.77
74Type 1 diabetes mellitusEnrichmentFOXP31.70
75Il10-related early-onset inflammatory bowel diseaseEnrichmentIL101.70
76MyelofibrosisEnrichmentJAK21.63
77Essential thrombocythemiaEnrichmentJAK21.63
78Narcolepsy 1EnrichmentTNFSF41.57
79Hypoplastic left heart syndromeEnrichmentNOTCH11.57
80Cataract - microcornea syndromeEnrichmentMAF1.57
81Rheumatoid arthritisEnrichmentIL101.52
82Leukemia, acute lymphoblastic 3EnrichmentJAK21.52
83Hydrops fetalisEnrichmentFOXP31.52
84Cataract 30, multiple typesEnrichmentMAF1.48
85Omenn syndromeEnrichmentIL2RG1.48
86Aplastic anemiaEnrichmentIFNG1.48
87Combined immunodeficiencyEnrichmentIL2RG1.44
88IchthyosisEnrichmentIL2RB1.44
89Combined t cell and b cell immunodeficiencyEnrichmentIL2RG1.44
90Combined t and b cell immunodeficiencyEnrichmentIL2RG1.44
91Aortic valve disease 1EnrichmentNOTCH11.36
92Nk-cell enteropathyEnrichmentJAK31.36
93Aortic aneurysm, familial thoracic 1EnrichmentNOTCH11.33
94Heart, malformation ofEnrichmentJAG11.23
95Centronuclear myopathyEnrichmentFOXP31.16
96HepatoblastomaEnrichmentJAG11.16
97Myocardial infarctionEnrichmentTNFSF41.14
98Developmental and epileptic encephalopathy 1EnrichmentMAF1.09
99Severe covid-19EnrichmentJAK31.03
100Connective tissue diseaseEnrichmentNOTCH10.99
101CakutEnrichmentGATA30.96
102Leukemia, acute myeloidEnrichmentJAK20.90
103Benign epilepsy with centrotemporal spikesEnrichmentMAF0.89
104Type 2 diabetes mellitusEnrichmentRBPJ0.88
105Centralopathic epilepsyEnrichmentMAF0.87
106West syndromeEnrichmentMAF0.86
107Familial thoracic aortic aneurysm and aortic dissectionEnrichmentNOTCH10.86
108Primary ovarian insufficiencyEnrichmentJAK20.74
109Breast cancerEnrichmentIL20.65
110Hereditary retinal dystrophyEnrichmentJAG10.20
111Fundus dystrophyEnrichmentJAG10.20

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