MAOA, monoamine oxidase A, 4128

N. diseases: 300; N. variants: 15
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0796275
Disease: Brunner Syndrome
Brunner Syndrome
0.910 Biomarker disease GENOMICS_ENGLAND New insights into Brunner syndrome and potential for targeted therapy. 25807999 2016
CUI: C0796275
Disease: Brunner Syndrome
Brunner Syndrome
0.910 Biomarker disease GENOMICS_ENGLAND The International Working Group on Neurotransmitter related Disorders (iNTD): A worldwide research project focused on primary and secondary neurotransmitter disorders. 27830117 2016
CUI: C0796275
Disease: Brunner Syndrome
Brunner Syndrome
0.910 Biomarker disease GENOMICS_ENGLAND It is the case of the X-linked gene encoding monoamine oxidase A (MAOA), for which only one nonsense mutation has been identified in Brunner syndrome, characterized in a single family by mild non-dysmorphic ID and impulsive, violent and aggressive behaviors. 24169519 2014
CUI: C0796275
Disease: Brunner Syndrome
Brunner Syndrome
0.910 GeneticVariation disease BEFREE It is the case of the X-linked gene encoding monoamine oxidase A (MAOA), for which only one nonsense mutation has been identified in Brunner syndrome, characterized in a single family by mild non-dysmorphic ID and impulsive, violent and aggressive behaviors. 24169519 2014
CUI: C0796275
Disease: Brunner Syndrome
Brunner Syndrome
0.910 Biomarker disease GENOMICS_ENGLAND It is the case of the X-linked gene encoding monoamine oxidase A (MAOA), for which only one nonsense mutation has been identified in Brunner syndrome, characterized in a single family by mild non-dysmorphic ID and impulsive, violent and aggressive behaviors. 24169519 2014
CUI: C0796275
Disease: Brunner Syndrome
Brunner Syndrome
0.910 GermlineCausalMutation disease ORPHANET It is the case of the X-linked gene encoding monoamine oxidase A (MAOA), for which only one nonsense mutation has been identified in Brunner syndrome, characterized in a single family by mild non-dysmorphic ID and impulsive, violent and aggressive behaviors. 24169519 2014
CUI: C0796275
Disease: Brunner Syndrome
Brunner Syndrome
0.910 Biomarker disease MGD This mutation is analogous to the cause of a rare human disorder, Brunner syndrome, characterized by complete MAO A deficiency and impulsive aggressiveness. 18418249 2008
CUI: C0796275
Disease: Brunner Syndrome
Brunner Syndrome
0.910 Biomarker disease MGD Aggressive behavior and altered amounts of brain serotonin and norepinephrine in mice lacking MAOA. 7792602 1995
CUI: C0796275
Disease: Brunner Syndrome
Brunner Syndrome
0.910 GermlineCausalMutation disease ORPHANET Abnormal behavior associated with a point mutation in the structural gene for monoamine oxidase A. 8211186 1993
CUI: C0796275
Disease: Brunner Syndrome
Brunner Syndrome
0.910 GeneticVariation disease CLINVAR
CUI: C0796275
Disease: Brunner Syndrome
Brunner Syndrome
0.910 Biomarker disease CTD_human
CUI: C0796275
Disease: Brunner Syndrome
Brunner Syndrome
0.910 CausalMutation disease CLINVAR