Brunner Syndrome MeSH Supplementary Concept Data 2025

Details
Concepts

MeSH Supplementary: Brunner Syndrome
Unique ID: C563156
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C563156
Registry Numbers: 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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