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
|