Ethanol effects on histone modifications

No Pathway Network information available for Ethanol effects on histone modifications

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

Disorders associated with Ethanol effects on histone modifications SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Alcohol dependenceEnrichmentADH1B, ADH1C, ALDH26.67
2Neural tube defects, folate-sensitiveEnrichmentMTHFR, MTR4.52
3Chondrodysplasia with platyspondyly, distinctive brachydactyly, hydrocephaly, and microphthalmiaEnrichmentHDAC62.64
4Homocystinuria due to deficiency of n -methylenetetrahydrofolate reductase activityEnrichmentMTHFR2.64
5Hypermethioninemia with s-adenosylhomocysteine hydrolase deficiencyEnrichmentAHCY2.64
6Chromosome 2q37 deletion syndromeEnrichmentHDAC42.64
7Auriculocondylar syndrome 4EnrichmentHDAC92.64
8Cornelia de lange syndrome 5EnrichmentHDAC82.64
9Megaloblastic anemia, folate-responsiveEnrichmentSLC19A12.64
10Alcohol sensitivity, acuteEnrichmentALDH22.64
11Diaphragmatic hernia 4, with cardiovascular defectsEnrichmentALDH1A22.64
12Megaloblastic anemia due to dihydrofolate reductase deficiencyEnrichmentDHFR2.64
13Neurodevelopmental disorder with central hypotonia and dysmorphic faciesEnrichmentHDAC42.64
14Immunodeficiency 114, folate-responsiveEnrichmentSLC19A12.64
15Methionine adenosyltransferase i/iii deficiencyEnrichmentMAT1A2.34
16Syndactyly, type iiiEnrichmentHDAC82.34
17Amed syndrome, digenicEnrichmentALDH22.34
18Wilson-turner syndromeEnrichmentHDAC82.34
19Microphthalmia, isolated 8EnrichmentALDH1A32.34
20Glaucoma, primary closed-angleEnrichmentSLC19A12.34
21Disorders of intracellular cobalamin metabolismEnrichmentMTR2.34
22Dyskeratosis congenita, digenicEnrichmentTYMS2.34
23Isolated anencephalyEnrichmentMTHFR2.34
24Isolated exencephalyEnrichmentMTHFR2.34
25Methionine adenosyltransferase deficiencyEnrichmentMAT1A2.34
26Homocystinuria-megaloblastic anemia, cblg typeEnrichmentMTR2.16
27Familial adenomatous polyposis 4EnrichmentDHFR2.16
28Isolated anophthalmia-microphthalmia syndromeEnrichmentALDH1A32.16
29HomocystinuriaEnrichmentMTR2.16
30Parkinson disease, mitochondrialEnrichmentADH1C2.04
31Knobloch syndromeEnrichmentSLC19A12.04
32Knobloch syndrome 1EnrichmentSLC19A11.94
33Thrombophilia due to thrombin defectEnrichmentMTHFR1.80
34Fanconi anemia, complementation group cEnrichmentHDAC81.74
35Orofacial cleft 1EnrichmentACSS21.69
36Cornelia de lange syndrome 1EnrichmentHDAC81.69
37Cornelia de lange syndromeEnrichmentHDAC81.69
38NanophthalmosEnrichmentALDH1A31.60
39Atrial heart septal defectEnrichmentHDAC81.60
40Interatrial communicationEnrichmentHDAC81.60
41Neural tube defectsEnrichmentMTHFR1.53
42CataractEnrichmentSLC19A11.50
43Polycystic kidney diseaseEnrichmentHDAC81.39
44Dyskeratosis congenitaEnrichmentTYMS1.37
45Macs syndromeEnrichmentALDH1A31.35
46Endometrial cancerEnrichmentDHFR1.33
47MicrophthalmiaEnrichmentALDH1A31.31
48Parkinson disease, late-onsetEnrichmentADH1C1.27
49Stargardt disease 1EnrichmentSLC19A11.18
50Lung cancerEnrichmentSLC19A11.15
51EpilepsyEnrichmentMTR1.06
52West syndromeEnrichmentMTHFR1.02
53Myeloma, multipleEnrichmentHDAC40.92
54SchizophreniaEnrichmentMTHFR0.90
55AutismEnrichmentALDH1A30.82
56MicrocephalyEnrichmentHDAC80.61
57Inherited cancer-predisposing syndromeEnrichmentDHFR0.58
58Retinitis pigmentosaEnrichmentSLC19A10.41
59Hereditary retinal dystrophyEnrichmentSLC19A10.31
60Fundus dystrophyEnrichmentSLC19A10.31

Loading...
Loading...
Loading...