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Brunner Syndrome MeSH Supplementary Concept Data 2024


MeSH Supplementary
Brunner Syndrome
Unique ID
C563156
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/C563156
Registry Number
0
Heading Mapped to
Aggression
*Disruptive, Impulse Control, and Conduct Disorders
*Intellectual Disability
Monoamine Oxidase / *deficiency
*Genetic Diseases, X-Linked
Frequency
3
Note
mutation in monoamine oxidase A (MAOA)
Date of Entry
2012/11/05
Revision Date
2016/07/07
Brunner Syndrome Preferred
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