Statements (24)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
gptkb:genetic_disorder
gptkb: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 |
| 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 |
8
|
| https://www.w3.org/2000/01/rdf-schema#label |
Brunner syndrome
|