OBO ID: DOID:0060693
Term Name: Brunner Syndrome Search Ontology:
Synonyms:
  • monoamine oxidase A deficiency
Definition: An amino acid metabolic disorder characterized by recessive X-linked inhetiance, impaired monoamine metabolism, impulsive aggressiveness and mild mental retardation that has_material_basis_in mutation in the MAOA gene on chromosome Xp11. (2)
References:
Ontology: Human Disease   ( DOID:0060693 )
Relationships
is a type of:
OTHER Brunner Syndrome PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
MAOA {Antisocial behavior} 300615
Brunner syndrome 300615
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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