MAOA, monoamine oxidase A, 4128

N. diseases: 300; N. variants: 15
Disease: Sudden infant death syndrome ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0038644
Disease: Sudden infant death syndrome
Sudden infant death syndrome 		0.370 GeneticVariation disease BEFREE This study clearly disproves interactions between MAOA promoter polymorphisms and SIDS, even if variations in single nucleotide polymorphisms of MAOA should be subjected to further analysis to clarify their impact on SIDS. 24173666 2014
CUI: C0038644
Disease: Sudden infant death syndrome
Sudden infant death syndrome 		0.370 GeneticVariation disease BEFREE This article indicates that neither the VNTR in the promoter of the MAOA gene, nor rs25531 in the gene encoding 5-HTT, is involved in SIDS. 24286237 2014
CUI: C0038644
Disease: Sudden infant death syndrome
Sudden infant death syndrome 		0.370 GeneticVariation disease BEFREE However, with the complex and inconsistent evidence available to date, the impact of the MAO-A promoter polymorphism on SIDS etiology remains unclear. 23391042 2013
CUI: C0038644
Disease: Sudden infant death syndrome
Sudden infant death syndrome 		0.370 GeneticVariation disease BEFREE Our results indicate a relationship between SIDS and the MAOA genotype in boys via influencing serotonergic and noradrenergic neurons in the brainstem. 22351881 2012
CUI: C0038644
Disease: Sudden infant death syndrome
Sudden infant death syndrome 		0.370 Biomarker disease BEFREE Considering correspondence between 5HTT and MAOA in IALTE and SIDS, we hypothesize that the 2 syndromes are different expressions of a common ethiopathogenesis. 22711722 2012
CUI: C0038644
Disease: Sudden infant death syndrome
Sudden infant death syndrome 		0.370 Biomarker disease GENOMICS_ENGLAND Our results indicate a relationship between SIDS and the MAOA genotype in boys via influencing serotonergic and noradrenergic neurons in the brainstem. 22351881 2012
CUI: C0038644
Disease: Sudden infant death syndrome
Sudden infant death syndrome 		0.370 Biomarker disease BEFREE Findings are discussed considering the metabolic association among DAT, 5-HTT and MAOA with special emphasis on the linked action of 5-HTT/MAOA in regulating serotonin metabolism of SIDS and SIUD infants. 18810510 2009
CUI: C0038644
Disease: Sudden infant death syndrome
Sudden infant death syndrome 		0.370 Biomarker disease LHGDN Genes regulating the serotonin metabolic pathway in the brain stem and their role in the etiopathogenesis of the sudden infant death syndrome. 18387780 2008