Interleukin-11 signaling pathway

No Pathway Network information available for Interleukin-11 signaling pathway

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

Disorders associated with Interleukin-11 signaling pathway SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Noonan syndrome and noonan-related syndromeEnrichmentHRAS, MAP2K1, MAP2K2, PTPN11, RAF19.08
2Noonan syndrome 1EnrichmentHRAS, MAP2K1, MAP2K2, PTPN11, RAF18.04
3RasopathyEnrichmentHRAS, MAP2K1, MAP2K2, PTPN11, RAF17.75
4Breast implant-associated anaplastic large cell lymphomaEnrichmentJAK1, JAK2, STAT37.50
5Noonan syndrome 3EnrichmentHRAS, PTPN11, RAF15.96
6Melanoma of soft tissueEnrichmentATF1, CREB14.51
7Cardiofaciocutaneous syndrome 1EnrichmentMAP2K1, MAP2K24.21
8Cardiofaciocutaneous syndromeEnrichmentMAP2K1, MAP2K24.21
9Noonan syndrome with multiple lentiginesEnrichmentPTPN11, RAF14.21
10MyelofibrosisEnrichmentJAK2, SRC3.67
11Melanocytic nevus syndrome, congenitalEnrichmentHRAS, RAF13.55
12Arteriovenous malformationEnrichmentHRAS, MAP2K13.44
13Myopathy, x-linked, with excessive autophagyEnrichmentHRAS, MAP2K13.34
14Lung non-small cell carcinomaEnrichmentHRAS, MAP2K13.26
15Specific learning disabilityEnrichmentMAPK1, PTPN113.26
16Colorectal cancerEnrichmentAKT1, PIK3R1, SRC2.55
17Hydrops fetalis, nonimmuneEnrichmentHRAS, PTPN112.50
18Proteus syndromeEnrichmentAKT12.49
19MetachondromatosisEnrichmentPTPN112.49
20Immunodeficiency 35EnrichmentTYK22.49
21Noonan syndrome 5EnrichmentRAF12.49
22Melorheostosis, isolatedEnrichmentMAP2K12.49
23Dermatitis, atopic, 4EnrichmentSOCS32.49
24Leopard syndrome 1EnrichmentPTPN112.49
25Cardiomyopathy, dilated, 1nnEnrichmentRAF12.49
26Cardiofaciocutaneous syndrome 3EnrichmentMAP2K12.49
27Fetal encasement syndromeEnrichmentCHUK2.49
28Craniosynostosis and dental anomaliesEnrichmentIL11RA2.49
29Immunodeficiency 15bEnrichmentIKBKB2.49
30Stuve-wiedemann syndrome 2EnrichmentIL6ST2.49
31Noonan syndrome 13EnrichmentMAPK12.49
32Hyper-ige syndrome 4a, autosomal dominant, with recurrent infectionsEnrichmentIL6ST2.49
33Parkinson disease 25, autosomal recessive early-onset, with impaired intellectual developmentEnrichmentPTPA2.49
34Immunodeficiency 15aEnrichmentIKBKB2.49
35Short syndromeEnrichmentPIK3R12.49
36T-cell large granular lymphocyte leukemiaEnrichmentSTAT32.49
37MelorheostosisEnrichmentMAP2K12.49
38Leopard syndrome 2EnrichmentRAF12.49
39Immunodeficiency 31aEnrichmentSTAT12.49
40Immunodeficiency 36 with lymphoproliferationEnrichmentPIK3R12.49
41Cardiofaciocutaneous syndrome 4EnrichmentMAP2K22.49
42Cowden syndrome 6EnrichmentAKT12.49
43Agammaglobulinemia 7, autosomal recessiveEnrichmentPIK3R12.49
44Immunodeficiency 31bEnrichmentSTAT12.49
45Autoimmune disease, multisystem, infantile-onset, 1EnrichmentSTAT32.49
46Thrombocytopenia 6EnrichmentSRC2.49
47Hyper-ige syndrome 4b, autosomal recessive, with recurrent infectionsEnrichmentIL6ST2.49
48Immunodeficiency 94 with autoinflammation and dysmorphic faciesEnrichmentIL6ST2.49
49Bartsocas-papas syndrome 2EnrichmentCHUK2.49
50TrigonitisEnrichmentRAF12.49
51Stat3-related early-onset multisystem autoimmune diseaseEnrichmentSTAT32.49
52Fetomaternal alloimmune thrombocytopenia 3EnrichmentITGA22.49
53Combined immunodeficiency-hypogammaglobulinemia-skeletal anomalies syndrome due to ikbka deficiencyEnrichmentCHUK2.49
54Phakomatosis pigmentokeratoticaEnrichmentHRAS2.49
55Chronic lymphoproliferative disorder of natural killer cellsEnrichmentSTAT32.49
56Mendelian susceptibility to mycobacterial diseases due to partial jak1 deficiencyEnrichmentJAK12.49
57Malignant astrocytomaEnrichmentPTPN112.49
58Non-immune hydrops fetalisEnrichmentHRAS, PTPN112.35
59Metaphyseal dysplasia with maxillary hypoplasia with or without brachydactylyEnrichmentRUNX22.19
60Camurati-engelmann disease 1EnrichmentTGFB12.19
61Costello syndromeEnrichmentHRAS2.19
62Histiocytoma, angiomatoid fibrousEnrichmentCREB12.19
63Thrombocythemia 3EnrichmentJAK22.19
64Immunodeficiency 31cEnrichmentSTAT12.19
65Werner syndromeEnrichmentPTPN112.19
66Autoinflammatory disease, familial, behcet-like 3EnrichmentRELA2.19
67Inflammatory bowel disease, immunodeficiency, and encephalopathyEnrichmentTGFB12.19
68Intravascular large b-cell lymphomaEnrichmentBCL22.19
69Rela fusion-positive ependymomaEnrichmentRELA2.19
70Camurati-engelmann diseaseEnrichmentTGFB12.19
71Autoinflammation, immune dysregulation, and eosinophiliaEnrichmentJAK12.19
72PolycythemiaEnrichmentJAK22.19
73Lymphomatoid papulosisEnrichmentTYK22.19
74Hypereosinophilic syndromeEnrichmentJAK22.19
75Tafro syndromeEnrichmentMAP2K22.19
76Primary cutaneous anaplastic large cell lymphomaEnrichmentTYK22.19
77Wooly hair nevusEnrichmentHRAS2.19
78Cleidocranial dysplasia 1EnrichmentRUNX22.01
79Hyper-ige syndrome 1, autosomal dominant, with recurrent infectionsEnrichmentSTAT32.01
80Polycythemia veraEnrichmentJAK22.01
81Stuve-wiedemann syndrome 1EnrichmentIL6ST2.01
82Langerhans cell histiocytosisEnrichmentMAP2K12.01
83Congenital lipomatous overgrowth, vascular malformations, and epidermal neviEnrichmentPIK3R12.01
84Immunodeficiency 14a with lymphoproliferation, autosomal dominantEnrichmentPIK3R12.01
85Large congenital melanocytic nevusEnrichmentHRAS2.01
86Hyper ige syndromeEnrichmentSTAT32.01
87High-grade b-cell lymphoma double-hit/triple-hitEnrichmentBCL22.01
88Immunodeficiency 14EnrichmentPIK3R12.01
89Cleidocranial dysplasiaEnrichmentRUNX22.01
90SpermatocytomaEnrichmentHRAS2.01
91Tricuspid valve insufficiencyEnrichmentPTPN112.01
92Stüve-wiedemann syndromeEnrichmentIL6ST2.01
93ThrombocytopeniaEnrichmentPTPN11, SRC1.98
94Erythrocytosis, familial, 1EnrichmentJAK21.89
95Schimmelpenning-feuerstein-mims syndromeEnrichmentHRAS1.89
96Budd-chiari syndromeEnrichmentJAK21.89
97Neurofibromatosis-noonan syndromeEnrichmentMAP2K21.89
98Megalencephaly-capillary malformation-polymicrogyria syndromeEnrichmentPIK3R21.89
99Chromosome 22q11.2 deletion syndrome, distalEnrichmentMAPK11.89
100Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 1EnrichmentPIK3R21.89
101Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemiaEnrichmentPTPN111.89
102Epidermolytic nevusEnrichmentHRAS1.89
103Cerebral malariaEnrichmentICAM11.89
104Follicular lymphomaEnrichmentBCL21.79
105LymphomaEnrichmentPTPN111.79
106Myeloproliferative neoplasmEnrichmentJAK21.79
107Inflammatory bowel disease 25, autosomal recessiveEnrichmentTGFB11.71
108Patent ductus arteriosusEnrichmentPTPN111.71
109Chronic mucocutaneous candidiasisEnrichmentSTAT11.71
110Fetomaternal alloimmune thrombocytopenia 1EnrichmentITGA21.71
111Il10-related early-onset inflammatory bowel diseaseEnrichmentTGFB11.71
112Breast adenocarcinomaEnrichmentAKT11.71
113Nevus, epidermalEnrichmentHRAS1.65
114Thyroid cancer, nonmedullary, 2EnrichmentHRAS1.65
115Capillary malformation-arteriovenous malformation 1EnrichmentMAP2K11.65
116Essential thrombocythemiaEnrichmentJAK21.65
117Pilomyxoid astrocytomaEnrichmentRAF11.65
118Follicular thyroid carcinomaEnrichmentHRAS1.65
119Overgrowth syndromeEnrichmentPIK3R11.65
120Permanent neonatal diabetes mellitusEnrichmentSTAT31.59
121Leukemia, acute lymphoblastic 3EnrichmentJAK21.54
122Cowden syndromeEnrichmentAKT11.54
123Autosomal non-syndromic agammaglobulinemiaEnrichmentPIK3R11.50
124Pectus excavatumEnrichmentPTPN111.45
125EpicanthusEnrichmentPTPN111.42
126Juvenile myelomonocytic leukemiaEnrichmentPTPN111.42
127MeningiomaEnrichmentAKT11.42
128Lip and oral cavity carcinomaEnrichmentHRAS1.42
129Congenital long qt syndromeEnrichmentPTPN111.42
130Acute promyelocytic leukemiaEnrichmentSTAT31.38
131OsteoporosisEnrichmentSRC1.35
132Autism spectrum disorderEnrichmentMAP2K1, PTPN111.31
133RhabdomyosarcomaEnrichmentHRAS1.30
134Heart, malformation ofEnrichmentMAPK11.25
135Patent foramen ovaleEnrichmentPTPN111.25
136Diffuse large b-cell lymphomaEnrichmentSTAT31.22
137MicrocephalyEnrichmentMAPK1, PTPN111.22
138CraniosynostosisEnrichmentIL11RA1.20
139MalariaEnrichmentICAM11.14
140Cardiomyopathy, familial hypertrophic, 1EnrichmentRAF11.12
141ScoliosisEnrichmentPTPN111.12
142StrabismusEnrichmentPTPN111.08
143Bladder cancerEnrichmentHRAS1.05
144Differentiated thyroid carcinomaEnrichmentHRAS1.05
145Long qt syndrome 1EnrichmentPTPN111.03
146Cystic fibrosisEnrichmentTGFB11.01
147Familial hypertrophic cardiomyopathyEnrichmentRAF10.99
148NephronophthisisEnrichmentPIAS10.99
149Severe combined immunodeficiencyEnrichmentIKBKB0.99
150Left ventricular noncompactionEnrichmentRAF10.97
151Leukemia, acute myeloidEnrichmentJAK20.91
152Nephrotic syndromeEnrichmentRUNX20.88
153Hypertrophic cardiomyopathyEnrichmentPTPN110.88
154Hereditary breast carcinomaEnrichmentAKT10.87
155Familial isolated dilated cardiomyopathyEnrichmentRAF10.80
156Myeloma, multipleEnrichmentPIK3R20.78
157Male infertility with azoospermia or oligozoospermia due to single gene mutationEnrichmentPTPN110.78
158Primary ovarian insufficiencyEnrichmentJAK20.76
159Breast cancerEnrichmentAKT10.66
160Dilated cardiomyopathyEnrichmentRAF10.64
161Ovarian cancerEnrichmentAKT10.55
162Inherited cancer-predisposing syndromeEnrichmentPTPN110.46

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