FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term Brunner Syndrome ID (Ontology) DOID:0060693 (Human Disease)
Definition An amino acid metabolic disorder characterized by recessive X-linked inheritance, impaired monoamine metabolism, impulsive aggressiveness and mild mental retardation that has_material_basis_in mutation in the MAOA gene on chromosome Xp11.
Also Known As "monoamine oxidase A deficiency"
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 Genes
 Brunner Syndrome       1
 for disease ribbon | Brunner Syndrome       1
 model of | Brunner Syndrome       1
Spanning Tree (Parents/Children)
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X-linked monogenic disease
 |__X-linked recessive disease_____
inherited metabolic disorder       |
 |__amino acid metabolic disorder__|
                                   Brunner Syndrome  1 rec.
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Is a X-linked recessive disease
amino acid metabolic disorder
Part of
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Synonyms
  • "monoamine oxidase A deficiency" EXACT
Secondary IDs
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ICD10CM:E70.8
MESH:C563156
MIM:300615
ORDO:3057