Nonalcoholic fatty liver disease

No Pathway Network information available for Nonalcoholic fatty liver disease

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

Disorders associated with Nonalcoholic fatty liver disease SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Type 2 diabetes mellitusEnrichmentIL6, INSR, IRS1, IRS24.93
2Autoimmune lymphoproliferative syndromeEnrichmentFAS, FASLG4.17
3Leptin deficiency or dysfunctionEnrichmentLEP, LEPR4.17
4Type 1 diabetes mellitusEnrichmentIL6, INS3.78
5Lung cancerEnrichmentCASP8, FAS, FASLG3.77
6Multiple sclerosisEnrichmentNR1H3, TNFRSF1A3.00
7Behcet syndromeEnrichmentFAS, TNFRSF1A2.73
8Periodic fever, familial, autosomal dominantEnrichmentTNFRSF1A2.47
9Adenosine triphosphate, elevated, of erythrocytesEnrichmentPKLR2.47
10Donohue syndromeEnrichmentINSR2.47
11Anemia, congenital, nonspherocytic hemolytic, 2EnrichmentPKLR2.47
12Hyperinsulinemic hypoglycemia, familial, 5EnrichmentINSR2.47
13Pineal hyperplasia, insulin-resistant diabetes mellitus, and somatic abnormalitiesEnrichmentINSR2.47
14Diabetes mellitus, insulin-resistant, with acanthosis nigricansEnrichmentINSR2.47
15Caspase 8 deficiencyEnrichmentCASP82.47
16Dermatitis, atopic, 4EnrichmentSOCS32.47
17Mucoepithelial dysplasia, hereditaryEnrichmentSREBF12.47
18Immunodeficiency 15bEnrichmentIKBKB2.47
19Immunodeficiency 15aEnrichmentIKBKB2.47
20Ifap syndrome 2EnrichmentSREBF12.47
21Thrombocytopenia 4EnrichmentCYCS2.47
22Major affective disorder 7EnrichmentXBP12.47
23Autoimmune disease, multisystem, with facial dysmorphismEnrichmentITCH2.47
24Interleukin 6, serum level of, quantitative trait locusEnrichmentIL6R2.47
25Soluble interleukin-6 receptor, serum level of, quantitative trait locusEnrichmentIL6R2.47
26Multiple sclerosis 5EnrichmentTNFRSF1A2.47
27Hyper-ige syndrome 5, autosomal recessive, with recurrent infectionsEnrichmentIL6R2.47
28Colorectal cancer 3EnrichmentSMAD72.47
29Cholestasis, progressive familial intrahepatic, 5EnrichmentNR1H42.47
30Leptin receptor deficiencyEnrichmentLEPR2.47
31Tnf receptor-associated periodic fever syndromeEnrichmentTNFRSF1A2.47
32Syndromic multisystem autoimmune disease due to itch deficiencyEnrichmentITCH2.47
33Acute myeloid leukemia with mutated cebpaEnrichmentCEBPA2.47
34Epiphyseal dysplasia, multiple, with early-onset diabetes mellitusEnrichmentEIF2AK32.17
35Hyperinsulinemic hypoglycemia, familial, 4EnrichmentINSR2.17
36Maturity-onset diabetes of the young, type 10EnrichmentINS2.17
37HyperproinsulinemiaEnrichmentINS2.17
38Immunodeficiency 127EnrichmentTNF2.17
39Diabetes mellitus, permanent neonatal, 4EnrichmentINS2.17
40Intermittent hydrarthrosisEnrichmentTNFRSF1A2.17
41Type 1 diabetes mellitus 2EnrichmentINS1.99
42Immunodeficiency 98 with autoinflammation, x-linkedEnrichmentFASLG1.99
43Ifap syndrome 1, with or without bresheck syndromeEnrichmentSREBF11.99
44Menkes diseaseEnrichmentEIF2AK31.99
45Psoriatic arthritisEnrichmentTNF1.99
46Adiponectin deficiencyEnrichmentADIPOQ1.99
47Myxoid liposarcomaEnrichmentDDIT31.99
48T-cell acute lymphoblastic leukemiaEnrichmentBAX1.99
49Migraine without auraEnrichmentTNF1.99
50Vogt-koyanagi-harada diseaseEnrichmentFAS1.99
51Kaposi sarcomaEnrichmentIL61.87
52Neonatal diabetes mellitusEnrichmentINS1.87
53Intrahepatic cholestasis of pregnancyEnrichmentNR1H41.87
54Cerebral malariaEnrichmentTNF1.87
55Systemic-onset juvenile idiopathic arthritisEnrichmentIL61.87
56Rheumatoid arthritis, systemic juvenileEnrichmentIL61.77
57Vascular dementiaEnrichmentTNF1.77
58Autosomal thrombocytopenia with normal plateletsEnrichmentCYCS1.77
59Inherited acute myeloid leukemiaEnrichmentCEBPA1.77
60Acute myeloid leukemia with t(8;21)(q22;q22) translocationEnrichmentCEBPA1.77
61Cholestasis, progressive familial intrahepatic, 1EnrichmentNR1H41.70
6246,xy disorder of sex developmentEnrichmentINSR1.70
63Hemolytic anemiaEnrichmentPKLR1.63
64Breast cancerEnrichmentCASP8, JUN1.57
65Permanent neonatal diabetes mellitusEnrichmentINS1.57
66Charge syndromeEnrichmentTNFRSF1A1.52
67Inflammatory bowel disease 1EnrichmentIL61.52
68Adult hepatocellular carcinomaEnrichmentCASP81.52
69AsthmaEnrichmentTNF1.44
70Diabetes mellitusEnrichmentINS1.44
71Alzheimer's diseaseEnrichmentTNF1.36
72Human immunodeficiency virus type 1EnrichmentCCL21.23
73Arteriovenous malformations of the brainEnrichmentIL61.20
74Maturity-onset diabetes of the youngEnrichmentINS1.18
75Hepatocellular carcinomaEnrichmentCASP81.14
76MalariaEnrichmentTNF1.12
77Autoinflammatory diseaseEnrichmentTNFRSF1A1.11
78Hirschsprung disease 1EnrichmentSREBF11.03
79Severe combined immunodeficiencyEnrichmentIKBKB0.97
80Systemic lupus erythematosusEnrichmentTNF0.91
81Leukemia, acute myeloidEnrichmentCEBPA0.90
82ThrombocytopeniaEnrichmentCYCS0.82
83Body mass index quantitative trait locus 11EnrichmentLEPR0.81
84Myeloma, multipleEnrichmentRXRA0.76
85Colorectal cancerEnrichmentBAX0.59
86Inherited cancer-predisposing syndromeEnrichmentCEBPA0.44

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