Interferon Pathway

No Pathway Network information available for Interferon Pathway

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

Disorders associated with Interferon Pathway SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Multisystem inflammatory syndrome in childrenEnrichmentIFNA21, IFNA4, IFNA6, IFNAR2, IFNB16.53
2Bryant-li-bhoj neurodevelopmental syndrome 2EnrichmentH3-3A, H3-3B4.35
3Breast implant-associated anaplastic large cell lymphomaEnrichmentJAK1, JAK23.88
4Immunodeficiency 44EnrichmentIFNAR2, STAT23.88
5Hepatitis bEnrichmentIFNAR2, IFNGR13.58
6Overgrowth syndromeEnrichmentMTOR, PIK3R13.04
7Glioma susceptibility 1EnrichmentH3-3A, H3C12.92
8Type 2 diabetes mellitusEnrichmentIL6, IRS1, IRS22.56
9Helicobacter pylori infectionEnrichmentIFNGR12.17
10Developmental and epileptic encephalopathy 8EnrichmentARHGEF92.17
11Immunodeficiency 35EnrichmentTYK22.17
1246,xy sex reversal 6EnrichmentMAP3K12.17
13Ataxia-oculomotor apraxia 3EnrichmentPIK3R52.17
14Autoimmune lymphoproliferative syndrome, type iiiEnrichmentPRKCD2.17
15Immunodeficiency 27aEnrichmentIFNGR12.17
16Immunodeficiency 62EnrichmentARHGEF12.17
17Immunodeficiency 69EnrichmentIFNG2.17
18Pseudo-torch syndrome 3EnrichmentSTAT22.17
19Neurodevelopmental disorder with midbrain and hindbrain malformationsEnrichmentARHGEF22.17
20Immunodeficiency 106 viral infectionsEnrichmentIFNAR12.17
21Short syndromeEnrichmentPIK3R12.17
22Intellectual developmental disorder, x-linked 46EnrichmentARHGEF62.17
23Autism 19EnrichmentEIF4E2.17
24Slowed nerve conduction velocity, autosomal dominantEnrichmentARHGEF102.17
25Immunodeficiency 27bEnrichmentIFNGR12.17
26Immunodeficiency 31aEnrichmentSTAT12.17
27Immunodeficiency 36 with lymphoproliferationEnrichmentPIK3R12.17
28Agammaglobulinemia 7, autosomal recessiveEnrichmentPIK3R12.17
29Immunodeficiency 31bEnrichmentSTAT12.17
30Brain small vessel disease 5 with osteoporosisEnrichmentARHGEF152.17
31Bryant-li-bhoj neurodevelopmental syndrome 1EnrichmentH3-3A2.17
32Immunodeficiency 65 viral infectionsEnrichmentIRF92.17
33Cerebral cavernous malformations 5EnrichmentMAP3K32.17
34Autosomal dominant mendelian susceptibility to mycobacterial diseases due to partial ifngammar2 deficiencyEnrichmentIFNGR22.17
35Microcephaly-corpus callosum and cerebellar vermis hypoplasia-facial dysmorphism-intellectual disability syndromEnrichmentRAC12.17
36Verrucous hemangiomaEnrichmentMAP3K32.17
37Mendelian susceptibility to mycobacterial diseases due to partial jak1 deficiencyEnrichmentJAK12.17
38Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 2EnrichmentPIK3R51.87
39Histiocytoma, angiomatoid fibrousEnrichmentCREB11.87
40Immunodeficiency 45EnrichmentIFNAR21.87
41Thrombocythemia 3EnrichmentJAK21.87
42Immunodeficiency 31cEnrichmentSTAT11.87
43Intellectual developmental disorder, autosomal dominant 48EnrichmentRAC11.87
44Cebalid syndromeEnrichmentMTOR1.87
45Autoinflammation, immune dysregulation, and eosinophiliaEnrichmentJAK11.87
46Smith-kingsmore syndromeEnrichmentMTOR1.87
47PolycythemiaEnrichmentJAK21.87
48Lymphomatoid papulosisEnrichmentTYK21.87
49Hypereosinophilic syndromeEnrichmentJAK21.87
50Primary cutaneous anaplastic large cell lymphomaEnrichmentTYK21.87
51Polycythemia veraEnrichmentJAK21.70
52Tuberous sclerosis 1EnrichmentIFNG1.70
53Hepatitis c virusEnrichmentIFNG1.70
54Congenital lipomatous overgrowth, vascular malformations, and epidermal neviEnrichmentPIK3R11.70
55Tuberous sclerosis 2EnrichmentIFNG1.70
56Immunodeficiency 14a with lymphoproliferation, autosomal dominantEnrichmentPIK3R11.70
57Immunodeficiency 28EnrichmentIFNGR21.70
58Immunodeficiency 14EnrichmentPIK3R11.70
59Melanoma of soft tissueEnrichmentCREB11.70
60Kaposi sarcomaEnrichmentIL61.58
61Erythrocytosis, familial, 1EnrichmentJAK21.58
62Diffuse gastric and lobular breast cancer syndromeEnrichmentMAP3K61.58
63Budd-chiari syndromeEnrichmentJAK21.58
64Megalencephaly-capillary malformation-polymicrogyria syndromeEnrichmentPIK3R21.58
65Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 1EnrichmentPIK3R21.58
66Focal cortical dysplasia, type iiEnrichmentMTOR1.58
67Systemic-onset juvenile idiopathic arthritisEnrichmentIL61.58
68Isolated focal cortical dysplasia type iiEnrichmentMTOR1.58
69Rheumatoid arthritis, systemic juvenileEnrichmentIL61.48
70Myeloproliferative neoplasmEnrichmentJAK21.48
71HemimegalencephalyEnrichmentMTOR1.48
72Idiopathic aplastic anemiaEnrichmentIFNG1.48
73Type 1 diabetes mellitusEnrichmentIL61.40
74Chronic mucocutaneous candidiasisEnrichmentSTAT11.40
75MyelofibrosisEnrichmentJAK21.34
76Renal cell carcinoma, papillary, 1EnrichmentMTOR1.34
77Essential thrombocythemiaEnrichmentJAK21.34
78Myeloma, multipleEnrichmentH3C1, PIK3R21.27
79Inflammatory bowel disease 1EnrichmentIL61.23
80Leukemia, acute lymphoblastic 3EnrichmentJAK21.23
81Neurodevelopmental disorder with dysmorphic facies and distal limb anomaliesEnrichmentRAC11.23
82Aplastic anemiaEnrichmentIFNG1.19
83Autosomal non-syndromic agammaglobulinemiaEnrichmentPIK3R11.19
8446,xy complete gonadal dysgenesisEnrichmentMAP3K11.15
8546,xy partial gonadal dysgenesisEnrichmentMAP3K11.05
86Renal cell carcinoma, nonpapillaryEnrichmentMTOR1.02
87Rare genetic intellectual disabilityEnrichmentMTOR1.02
88Human immunodeficiency virus type 1EnrichmentIFNG0.94
89Arteriovenous malformations of the brainEnrichmentIL60.92
90Behcet syndromeEnrichmentIFNGR10.92
91Non-syndromic x-linked intellectual disabilityEnrichmentARHGEF60.67
92Developmental and epileptic encephalopathyEnrichmentARHGEF150.67
93Leukemia, acute myeloidEnrichmentJAK20.63
94Charcot-marie-tooth diseaseEnrichmentARHGEF100.62
95Primary ovarian insufficiencyEnrichmentJAK20.48
96Colorectal cancerEnrichmentPIK3R10.35
97Ovarian cancerEnrichmentMAP3K10.31

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