Monoamine oxidase A deficiency Gene Set

Dataset ClinVar Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description Monoamine oxidase-A deficiency is a very rare recessive X-linked biogenic amine metabolism disorder characterized clinically by mild intellectual deficit, impulsive aggressiveness, and sometimes violent behavior and presenting from childhood. (Orphanet Rare Disease Ontology, Orphanet_3057)
External Link http://www.omim.org/entry/300615
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Genes

1 genes associated with the Monoamine oxidase A deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Symbol Name
MAOA monoamine oxidase A