Overview of nanoparticle effects

No Pathway Network information available for Overview of nanoparticle effects

Pathways in the Overview of nanoparticle effects SuperPath

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

Disorders associated with Overview of nanoparticle effects SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Ectodermal dysplasia, ectrodactyly, and macular dystrophy syndromeEnrichmentCDH32.85
2PorencephalyEnrichmentCOL4A12.85
3Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 2EnrichmentAKT32.85
4HypotrichosisEnrichmentCDH32.85
5Immunodeficiency 14b, autosomal recessiveEnrichmentPIK3CD2.85
6Heme oxygenase 1 deficiencyEnrichmentHMOX12.85
7Col4a1-related disordersEnrichmentCOL4A12.85
8Capillary hemangiomaEnrichmentAKT32.85
9Col4a1 or col4a2-related cerebral small vessel diseaseEnrichmentCOL4A12.85
10Spondyloepimetaphyseal dysplasia, strudwick typeEnrichmentFN12.55
11Spondylometaphyseal dysplasia, corner fracture typeEnrichmentFN12.55
12Epidermolysis bullosa, junctional 2c, laryngoonychocutaneousEnrichmentLAMA32.55
13Hypotrichosis, congenital, with juvenile macular dystrophyEnrichmentCDH32.55
14Roifman-chitayat syndromeEnrichmentPIK3CD2.55
15Epidermolysis bullosa, junctional 2a, intermediateEnrichmentLAMA32.55
16Intravascular large b-cell lymphomaEnrichmentBCL22.55
17Immunodeficiency 127EnrichmentTNF2.55
18Senior-loken syndrome 7EnrichmentAKT32.55
19Immune system diseaseEnrichmentPIK3CD2.55
20Bardet-biedl syndrome 16EnrichmentAKT32.55
21Epidermolysis bullosa, junctional 2b, severeEnrichmentLAMA32.55
22Retinal arteries, tortuosity ofEnrichmentCOL4A12.38
23Glomerulopathy with fibronectin deposits 2EnrichmentFN12.38
24Psoriatic arthritisEnrichmentTNF2.38
25Immunodeficiency 14a with lymphoproliferation, autosomal dominantEnrichmentPIK3CD2.38
26Microangiopathy and leukoencephalopathy, pontine, autosomal dominantEnrichmentCOL4A12.38
27High-grade b-cell lymphoma double-hit/triple-hitEnrichmentBCL22.38
28Angiopathy, hereditary, with nephropathy, aneurysms, and muscle crampsEnrichmentCOL4A12.38
29Immunodeficiency 14EnrichmentPIK3CD2.38
30T-cell acute lymphoblastic leukemiaEnrichmentBAX2.38
31Migraine without auraEnrichmentTNF2.38
32Kaposi sarcomaEnrichmentIL62.25
33Brain small vessel disease 1 with or without ocular anomaliesEnrichmentCOL4A12.25
34SchizencephalyEnrichmentCOL4A12.25
35Megalencephaly-capillary malformation-polymicrogyria syndromeEnrichmentAKT32.25
36Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 1EnrichmentAKT32.25
37Cerebral malariaEnrichmentTNF2.25
38Systemic-onset juvenile idiopathic arthritisEnrichmentIL62.25
39Rheumatoid arthritis, systemic juvenileEnrichmentIL62.16
40Follicular lymphomaEnrichmentBCL22.16
41Vascular dementiaEnrichmentTNF2.16
42HemimegalencephalyEnrichmentAKT32.16
43Familial porencephalyEnrichmentCOL4A12.16
44Epidermolysis bullosa, junctional 1a, intermediateEnrichmentLAMA32.08
45Epidermolysis bullosa, junctional 1b, severeEnrichmentLAMA32.08
46Type 1 diabetes mellitusEnrichmentIL62.08
47Anterior segment dysgenesis 5EnrichmentCOL4A12.08
48Hemorrhage, intracerebralEnrichmentCOL4A12.08
49Junctional epidermolysis bullosa non-herlitz typeEnrichmentLAMA32.08
50KeratoconusEnrichmentCOL4A12.08
51MegacolonEnrichmentAKT32.01
52Inflammatory bowel disease 1EnrichmentIL61.90
53Junctional epidermolysis bullosaEnrichmentLAMA31.90
54Hypotrichosis simplexEnrichmentCDH31.90
55Peters-plus syndromeEnrichmentCOL4A11.86
56PolymicrogyriaEnrichmentAKT31.86
57Autosomal non-syndromic agammaglobulinemiaEnrichmentPIK3CD1.86
58AsthmaEnrichmentTNF1.82
59Pulmonary disease, chronic obstructiveEnrichmentHMOX11.74
60Alzheimer's diseaseEnrichmentTNF1.74
61Walker-warburg syndromeEnrichmentCOL4A11.71
62Corpus callosum, agenesis ofEnrichmentCOL4A11.68
63Anterior segment dysgenesisEnrichmentCOL4A11.68
64Isolated corpus callosum agenesisEnrichmentCOL4A11.68
65Intellectual disability-hypoplastic corpus callosum-preauricular tag syndromeEnrichmentCOL4A11.68
66Arteriovenous malformations of the brainEnrichmentIL61.58
67MalariaEnrichmentTNF1.50
68Cystic fibrosisEnrichmentHMOX11.36
69CakutEnrichmentCOL4A11.33
70Systemic lupus erythematosusEnrichmentTNF1.27
71Cerebral palsyEnrichmentCOL4A11.27
72Type 2 diabetes mellitusEnrichmentIL61.24
73Nephrotic syndromeEnrichmentFN11.23
74Colorectal cancerEnrichmentBAX0.94
75MicrocephalyEnrichmentCOL4A10.80
76Retinitis pigmentosaEnrichmentCDH30.59
77Hereditary retinal dystrophyEnrichmentCDH30.47
78Fundus dystrophyEnrichmentCDH30.47

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