MAOA, monoamine oxidase A, 4128

N. diseases: 300; N. variants: 15
Disease: Cognition Disorders ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0009241
Disease: Cognition Disorders
Cognition Disorders 		0.310 Biomarker group CTD_human Prenatal iron deficiency and monoamine oxidase A (MAOA) polymorphisms: combined risk for later cognitive performance in rhesus monkeys. 24402517 2014
CUI: C0009241
Disease: Cognition Disorders
Cognition Disorders 		0.310 GeneticVariation group BEFREE Lack of monoamine oxidase A (MAO-A) due to either Xp chromosomal deletions or alterations in the coding sequence of the gene for this enzyme are associated with marked changes in monoamine metabolism and appear to be associated with variable cognitive deficits and behavioral changes in humans and in transgenic mice. 9564605 1998