Brunner syndrome

GPTKB entity

Statements (24)
Predicate Object
gptkbp:instanceOf genetic disorder
rare disease
gptkbp:affects males
gptkbp:associatedWith monoamine oxidase A deficiency
gptkbp:causedBy mutation in MAOA gene
gptkbp:diagnosedBy genetic testing
gptkbp:firstDescribed 1993
Han G. Brunner
https://www.w3.org/2000/01/rdf-schema#label Brunner syndrome
gptkbp:ICD-10_code F60.8
gptkbp:inheritance X-linked recessive
gptkbp:locatedOnChromosome Xp11.3
gptkbp:namedAfter Han G. Brunner
gptkbp:OMIM 300615
gptkbp:prevalence extremely rare
gptkbp:symptom sleep disorders
aggressive behavior
impulsive behavior
hypersexuality
mild intellectual disability
gptkbp:treatment symptomatic management
gptkbp:bfsParent gptkb:MAO-A
gptkb:monoamine_oxidase_A
gptkbp:bfsLayer 7