Host-pathogen interaction of human corona viruses - ER stress

No Pathway Network information available for Host-pathogen interaction of human corona viruses - ER stress

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

Disorders associated with Host-pathogen interaction of human corona viruses - ER stress SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Olmsted syndrome, x-linkedEnrichmentMBTPS22.53
2Osteogenesis imperfecta, type xixEnrichmentMBTPS22.53
3Keratosis follicularis spinulosa decalvans, x-linkedEnrichmentMBTPS22.53
4Leukoencephalopathy, developmental delay, and episodic neurologic regression syndromeEnrichmentEIF2AK22.53
5Leukoencephalopathy, motor delay, spasticity, and dysarthria syndromeEnrichmentEIF2AK12.53
6Major affective disorder 7EnrichmentXBP12.53
7Cataract, alopecia, oral mucosal disorder, and psoriasis-like syndromeEnrichmentMBTPS12.53
8Achromatopsia 7EnrichmentATF62.53
9Microcephaly, short stature, and impaired glucose metabolism 2EnrichmentPPP1R15B2.53
10Noonan syndrome-like disorder with loose anagen hair 2EnrichmentPPP1CB2.53
11Dystonia 33EnrichmentEIF2AK22.53
12Ifap syndromeEnrichmentMBTPS22.53
13Bresek syndromeEnrichmentMBTPS22.53
14Immunodeficiency 108 with autoinflammationEnrichmentCEBPE2.42
15Cebpe-associated autoinflammation-immunodeficiency-neutrophil dysfunction syndromeEnrichmentCEBPE2.42
16Acute myeloid leukemia with mutated cebpaEnrichmentCEBPA2.42
17Epiphyseal dysplasia, multiple, with early-onset diabetes mellitusEnrichmentEIF2AK32.23
18Genitourinary and/or brain malformation syndromeEnrichmentPPP1R12A2.23
19Intravascular large b-cell lymphomaEnrichmentBCL22.23
20Leukodystrophy, hypomyelinating, 17EnrichmentEIF2AK12.23
21Noonan syndrome-like disorder with loose anagen hairEnrichmentPPP1CB2.23
22Primary microcephaly-mild intellectual disability-young-onset diabetes syndromeEnrichmentPPP1R15B2.23
23Spondyloepiphyseal dysplasia, kondo-fu typeEnrichmentMBTPS12.23
24Specific granule deficiency 1EnrichmentCEBPE2.12
25Specific granule deficiencyEnrichmentCEBPE2.12
26Ifap syndrome 1, with or without bresheck syndromeEnrichmentMBTPS22.05
27Menkes diseaseEnrichmentEIF2AK32.05
28Keratosis follicularis spinulosa decalvansEnrichmentMBTPS22.05
29High-grade b-cell lymphoma double-hit/triple-hitEnrichmentBCL22.05
30Torsion dystonia 1EnrichmentEIF2AK22.05
31Mutilating palmoplantar keratoderma with periorificial keratotic plaquesEnrichmentMBTPS22.05
32Myxoid liposarcomaEnrichmentDDIT32.05
33Follicular lymphomaEnrichmentBCL21.83
34Osteogenesis imperfecta, type iEnrichmentMBTPS21.76
35Inherited acute myeloid leukemiaEnrichmentCEBPA1.73
36Acute myeloid leukemia with t(8;21)(q22;q22) translocationEnrichmentCEBPA1.73
37AchromatopsiaEnrichmentATF61.54
38Lennox-gastaut syndromeEnrichmentMAPK101.53
39Osteogenesis imperfecta, type ivEnrichmentMBTPS21.42
40Osteogenesis imperfecta, type iiiEnrichmentMBTPS21.36
41Dandy-walker syndromeEnrichmentPPP1CB1.31
42Noonan syndrome 1EnrichmentPPP1CB1.18
43RasopathyEnrichmentPPP1CB1.13
44Type 2 diabetes mellitusEnrichmentPPP1R3A0.93
45Leukemia, acute myeloidEnrichmentCEBPA0.85
46Cone-rod dystrophy 2EnrichmentATF60.74
47Inherited cancer-predisposing syndromeEnrichmentCEBPA0.41
48Hereditary retinal dystrophyEnrichmentATF60.24
49Fundus dystrophyEnrichmentATF60.24

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