Th17 cell differentiation pathway

No Pathway Network information available for Th17 cell differentiation pathway

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

Disorders associated with Th17 cell differentiation pathway SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Severe combined immunodeficiencyEnrichmentCD247, CD3D, CD3E, CD3G, IKBKB, LCK, ZAP709.62
2Breast implant-associated anaplastic large cell lymphomaEnrichmentJAK1, JAK2, STAT36.90
3T-b+ severe combined immunodeficiency due to cd3delta/cd3epsilon/cd3zetaEnrichmentCD247, CD3D, CD3E6.90
4Immunodeficiency 31cEnrichmentIL21R, STAT14.59
5Loeys-dietz syndrome 1EnrichmentSMAD2, TGFBR14.12
6Type 1 diabetes mellitusEnrichmentFOXP3, IL63.42
7Chronic mucocutaneous candidiasisEnrichmentIL17F, STAT13.42
8Oligoarticular juvenile idiopathic arthritisEnrichmentCD247, IL2RA3.28
9Rheumatoid factor-negative juvenile idiopathic arthritisEnrichmentCD247, IL2RA3.28
10Inflammatory bowel disease 1EnrichmentIL6, PRKCQ3.05
11Loeys-dietz syndromeEnrichmentSMAD2, TGFBR13.05
12Acute promyelocytic leukemiaEnrichmentRARA, STAT32.72
13Behcet syndromeEnrichmentIFNGR1, IL23R2.38
14Helicobacter pylori infectionEnrichmentIFNGR12.29
15Type 1 diabetes mellitus 10EnrichmentIL2RA2.29
16Immunodysregulation, polyendocrinopathy, and enteropathy, x-linkedEnrichmentFOXP32.29
17Immunodeficiency 35EnrichmentTYK22.29
18Skin/hair/eye pigmentation, variation in, 8EnrichmentIRF42.29
19Dermatitis, atopic, 4EnrichmentSOCS32.29
20Multiple self-healing squamous epitheliomaEnrichmentTGFBR12.29
21Candidiasis, familial, 6EnrichmentIL17F2.29
22Immunodeficiency 27aEnrichmentIFNGR12.29
23Retinitis pigmentosa 85EnrichmentAHR2.29
24Immunodeficiency 15bEnrichmentIKBKB2.29
25Immunodeficiency 69EnrichmentIFNG2.29
26Noonan syndrome 13EnrichmentMAPK12.29
27Immunodeficiency 15aEnrichmentIKBKB2.29
28Hyper-ige syndrome 6, autosomal dominant, with recurrent infectionsEnrichmentSTAT62.29
29Immunodeficiency 131EnrichmentIRF42.29
30Developmental and epileptic encephalopathy 91EnrichmentPPP3CA2.29
31Arthrogryposis, cleft palate, craniosynostosis, and impaired intellectual developmentEnrichmentPPP3CA2.29
32Immunodeficiency 48EnrichmentZAP702.29
33Okt4 epitope deficiencyEnrichmentCD42.29
34Immune dysregulation, autoimmunity, and autoinflammationEnrichmentPLCG12.29
35Foveal hypoplasia 3EnrichmentAHR2.29
36T-cell large granular lymphocyte leukemiaEnrichmentSTAT32.29
37Immunodeficiency 18EnrichmentCD3E2.29
38Immunodeficiency 42EnrichmentRORC2.29
39Immunodeficiency 25EnrichmentCD2472.29
40Immunodeficiency 27bEnrichmentIFNGR12.29
41Psoriasis 7EnrichmentIL23R2.29
42Interleukin 6, serum level of, quantitative trait locusEnrichmentIL6R2.29
43Immunodeficiency 31aEnrichmentSTAT12.29
44Soluble interleukin-6 receptor, serum level of, quantitative trait locusEnrichmentIL6R2.29
45Hyper-ige syndrome 5, autosomal recessive, with recurrent infectionsEnrichmentIL6R2.29
46Loeys-dietz syndrome 6EnrichmentSMAD22.29
47Inflammatory bowel disease 17EnrichmentIL23R2.29
48Immunodeficiency 31bEnrichmentSTAT12.29
49Delayed sleep phase disorderEnrichmentCRY12.29
50Autoimmune disease, multisystem, infantile-onset, 2EnrichmentZAP702.29
51Immunodeficiency 22EnrichmentLCK2.29
52Autoimmune disease, multisystem, infantile-onset, 1EnrichmentSTAT32.29
53Immunodeficiency 79EnrichmentCD42.29
54Immunodeficiency 88EnrichmentTBX212.29
55Immunodeficiency 19, severe combinedEnrichmentCD3D2.29
56Congenital heart defects, multiple types, 8, with or without heterotaxyEnrichmentSMAD22.29
57Stat3-related early-onset multisystem autoimmune diseaseEnrichmentSTAT32.29
58Immunodeficiency 19EnrichmentCD3D2.29
59Whipple diseaseEnrichmentIRF42.29
60Chronic lymphoproliferative disorder of natural killer cellsEnrichmentSTAT32.29
61Mendelian susceptibility to mycobacterial diseases due to partial jak1 deficiencyEnrichmentJAK12.29
62Zap70-related severe combined immunodeficiencyEnrichmentZAP702.29
63Hypoparathyroidism, sensorineural deafness, and renal dysplasia syndromeEnrichmentGATA31.99
64Camurati-engelmann disease 1EnrichmentTGFB11.99
65Multinucleated neurons, anhydramnios, renal dysplasia, cerebellar hypoplasia, and hydranencephalyEnrichmentFOXP31.99
66Hemangiopericytoma, malignantEnrichmentSTAT61.99
67Immunodeficiency 41 with lymphoproliferation and autoimmunityEnrichmentIL2RA1.99
68Loeys-dietz syndrome 2EnrichmentTGFBR11.99
69Ectodermal dysplasia and immunodeficiency 2EnrichmentNFKBIA1.99
70Immunodeficiency, common variable, 12, with autoimmunityEnrichmentNFKB11.99
71Thrombocythemia 3EnrichmentJAK21.99
72Hypothyroidism, congenital, nongoitrous, 6EnrichmentNR1D11.99
73Cebalid syndromeEnrichmentMTOR1.99
74Inflammatory bowel disease, immunodeficiency, and encephalopathyEnrichmentTGFB11.99
75Immunodeficiency 56EnrichmentIL21R1.99
76Camurati-engelmann diseaseEnrichmentTGFB11.99
77Autoinflammation, immune dysregulation, and eosinophiliaEnrichmentJAK11.99
78Ectodermal dysplasia and immune deficiencyEnrichmentNFKBIA1.99
79Immunodeficiency 17EnrichmentCD3G1.99
80B-lymphoblastic leukemia/lymphoma with hyperdiploidyEnrichmentGATA31.99
81Smith-kingsmore syndromeEnrichmentMTOR1.99
82Hypoparathyroidism-deafness-renal disease syndromeEnrichmentGATA31.99
83Intellectual developmental disorder with or without epilepsy or cerebellar ataxiaEnrichmentRORA1.99
84PolycythemiaEnrichmentJAK21.99
85Immunodeficiency 52EnrichmentLAT1.99
86Lymphomatoid papulosisEnrichmentTYK21.99
87Autosomal dominant nonsyndromic deafnessEnrichmentGATA31.99
88Hypereosinophilic syndromeEnrichmentJAK21.99
89Common variable immunodeficiency 12EnrichmentNFKB11.99
90Primary cutaneous anaplastic large cell lymphomaEnrichmentTYK21.99
91Hyper-ige syndrome 1, autosomal dominant, with recurrent infectionsEnrichmentSTAT31.82
92Asthma, nasal polyps, and aspirin intoleranceEnrichmentTBX211.82
93Polycythemia veraEnrichmentJAK21.82
94Tuberous sclerosis 1EnrichmentIFNG1.82
95Hepatitis c virusEnrichmentIFNG1.82
96Nasopharyngeal carcinomaEnrichmentNFKBIA1.82
97Tuberous sclerosis 2EnrichmentIFNG1.82
98Hyper ige syndromeEnrichmentSTAT31.82
99Immunodeficiency, common variable, 11EnrichmentIL211.82
100End stage renal diseaseEnrichmentGATA31.82
101EnchondromatosisEnrichmentHIF1A1.82
102Kaposi sarcomaEnrichmentIL61.69
103Erythrocytosis, familial, 1EnrichmentJAK21.69
104Budd-chiari syndromeEnrichmentJAK21.69
105Chromosome 22q11.2 deletion syndrome, distalEnrichmentMAPK11.69
106Focal cortical dysplasia, type iiEnrichmentMTOR1.69
107Congenital generalized lipodystrophyEnrichmentFOS1.69
108Hepatitis bEnrichmentIFNGR11.69
109Aortic aneurysmEnrichmentTGFBR11.69
110Systemic-onset juvenile idiopathic arthritisEnrichmentIL61.69
111Isolated focal cortical dysplasia type iiEnrichmentMTOR1.69
112Familial thoracic aortic aneurysm and aortic dissectionEnrichmentSMAD2, TGFBR11.68
113Enchondromatosis, multiple, ollier typeEnrichmentHIF1A1.60
114Rheumatoid arthritis, systemic juvenileEnrichmentIL61.60
115Myeloproliferative neoplasmEnrichmentJAK21.60
116Histiocytoid hemangiomaEnrichmentFOS1.60
117HemimegalencephalyEnrichmentMTOR1.60
118Idiopathic aplastic anemiaEnrichmentIFNG1.60
119Inflammatory bowel disease 25, autosomal recessiveEnrichmentTGFB11.52
120Il10-related early-onset inflammatory bowel diseaseEnrichmentTGFB11.52
121Classic ehlers-danlos syndromeEnrichmentTGFBR11.52
122MyelofibrosisEnrichmentJAK21.45
123Renal cell carcinoma, papillary, 1EnrichmentMTOR1.45
124Multiple enchondromatosis, maffucci typeEnrichmentHIF1A1.45
125Essential thrombocythemiaEnrichmentJAK21.45
126Common variable immunodeficiencyEnrichmentNFKB11.45
127Overgrowth syndromeEnrichmentMTOR1.45
128Permanent neonatal diabetes mellitusEnrichmentSTAT31.40
129Leukemia, acute lymphoblastic 3EnrichmentJAK21.35
130Hydrops fetalisEnrichmentFOXP31.35
131Marfan syndromeEnrichmentTGFBR11.30
132Ciliary dyskinesia, primary, 3EnrichmentNFKB11.30
133Aplastic anemiaEnrichmentIFNG1.30
134Pectus excavatumEnrichmentTGFBR11.26
135Combined immunodeficiencyEnrichmentZAP701.26
136Combined t cell and b cell immunodeficiencyEnrichmentZAP701.26
137Specific learning disabilityEnrichmentMAPK11.26
138Combined t and b cell immunodeficiencyEnrichmentZAP701.26
139Breast cancerEnrichmentIL2, JUN1.25
140Renal cell carcinoma, nonpapillaryEnrichmentMTOR1.13
141Rare genetic intellectual disabilityEnrichmentMTOR1.13
142GliosarcomaEnrichmentNFKBIA1.11
143Giant cell glioblastomaEnrichmentNFKBIA1.08
144Heart, malformation ofEnrichmentMAPK11.06
145Human immunodeficiency virus type 1EnrichmentIFNG1.06
146Arteriovenous malformations of the brainEnrichmentIL61.03
147Diffuse large b-cell lymphomaEnrichmentSTAT31.03
148Centronuclear myopathyEnrichmentFOXP30.99
149Cystic fibrosisEnrichmentTGFB10.82
150CakutEnrichmentGATA30.80
151Leukemia, acute myeloidEnrichmentJAK20.73
152Type 2 diabetes mellitusEnrichmentIL60.71
153Gastric cancerEnrichmentIL1B0.71
154Autosomal dominant non-syndromic intellectual disabilityEnrichmentPPP3CA0.65
155Myeloma, multipleEnrichmentRXRA0.60
156Undetermined early-onset epileptic encephalopathyEnrichmentPPP3CA0.60
157Primary ovarian insufficiencyEnrichmentJAK20.58
158MicrocephalyEnrichmentMAPK10.33
159Complex neurodevelopmental disorderEnrichmentRORA0.33
160Retinitis pigmentosaEnrichmentAHR0.18

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