MAOA, monoamine oxidase A, 4128

N. diseases: 48; N. variants: 6
Disease: Brunner Syndrome ×
Source: CURATED ×
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 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 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 Biomarker disease CTD_human