Interferon type I signaling pathways

No Pathway Network information available for Interferon type I signaling pathways

Pathways in the Interferon type I signaling pathways SuperPath

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

Disorders associated with Interferon type I signaling pathways SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Severe combined immunodeficiencyEnrichmentLCK, PTPRC, ZAP705.81
2MetachondromatosisEnrichmentPTPN113.13
3Leopard syndrome 1EnrichmentPTPN113.13
4Immunodeficiency 48EnrichmentZAP703.13
5Immunodeficiency 105, severe combinedEnrichmentPTPRC3.13
6Autoimmune disease, multisystem, infantile-onset, 2EnrichmentZAP703.13
7Immunodeficiency 22EnrichmentLCK3.13
8Cd45 deficiencyEnrichmentPTPRC3.13
9Vegetative pyoderma gangrenosumEnrichmentPTPN63.13
10Bullous pyoderma gangrenosumEnrichmentPTPN63.13
11Pustular pyoderma gangrenosumEnrichmentPTPN63.13
12Classic pyoderma gangrenosumEnrichmentPTPN63.13
13Mendelian susceptibility to mycobacterial diseases due to partial jak1 deficiencyEnrichmentJAK13.13
14Zap70-related severe combined immunodeficiencyEnrichmentZAP703.13
15Malignant astrocytomaEnrichmentPTPN113.13
16Werner syndromeEnrichmentPTPN112.83
17Immunodeficiency 104, severe combinedEnrichmentPTPRC2.83
18Autoinflammation, immune dysregulation, and eosinophiliaEnrichmentJAK12.83
19Neutrophilic dermatosis, acute febrileEnrichmentPTPN62.66
20Breast implant-associated anaplastic large cell lymphomaEnrichmentJAK12.66
21Tricuspid valve insufficiencyEnrichmentPTPN112.66
22Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemiaEnrichmentPTPN112.53
23Noonan syndrome with multiple lentiginesEnrichmentPTPN112.53
24LymphomaEnrichmentPTPN112.43
25Patent ductus arteriosusEnrichmentPTPN112.35
26Noonan syndrome 3EnrichmentPTPN112.29
27Pectus excavatumEnrichmentPTPN112.09
28Combined immunodeficiencyEnrichmentZAP702.09
29Combined t cell and b cell immunodeficiencyEnrichmentZAP702.09
30Specific learning disabilityEnrichmentPTPN112.09
31Combined t and b cell immunodeficiencyEnrichmentZAP702.09
32EpicanthusEnrichmentPTPN112.05
33Juvenile myelomonocytic leukemiaEnrichmentPTPN112.05
34Congenital long qt syndromeEnrichmentPTPN112.05
35Noonan syndrome and noonan-related syndromeEnrichmentPTPN111.96
36Patent foramen ovaleEnrichmentPTPN111.88
37Noonan syndrome 1EnrichmentPTPN111.77
38ScoliosisEnrichmentPTPN111.76
39Hydrops fetalis, nonimmuneEnrichmentPTPN111.72
40RasopathyEnrichmentPTPN111.72
41StrabismusEnrichmentPTPN111.70
42Long qt syndrome 1EnrichmentPTPN111.66
43Non-immune hydrops fetalisEnrichmentPTPN111.65
44NephronophthisisEnrichmentPIAS11.62
45Hypertrophic cardiomyopathyEnrichmentPTPN111.50
46ThrombocytopeniaEnrichmentPTPN111.46
47Male infertility with azoospermia or oligozoospermia due to single gene mutationEnrichmentPTPN111.39
48Autism spectrum disorderEnrichmentPTPN111.11
49MicrocephalyEnrichmentPTPN111.06
50Inherited cancer-predisposing syndromeEnrichmentPTPN111.03

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