Huntington's disease-like syndrome
GPTKB entity
Statements (21)
Predicate | Object |
---|---|
gptkbp:instanceOf |
medical condition
|
gptkbp:causedBy |
various genetic mutations
|
gptkbp:differentialDiagnosis |
gptkb:Wilson's_disease
gptkb:Huntington's_disease gptkb:neuroacanthocytosis spinocerebellar ataxia |
gptkbp:firstDescribed |
1990s
|
https://www.w3.org/2000/01/rdf-schema#label |
Huntington's disease-like syndrome
|
gptkbp:inheritance |
autosomal dominant
autosomal recessive |
gptkbp:similarTo |
gptkb:Huntington's_disease
|
gptkbp:subspecies |
gptkb:HDL1
gptkb:HDL2 gptkb:HDL3 gptkb:HDL4_(SCA17) |
gptkbp:symptom |
cognitive decline
chorea psychiatric symptoms |
gptkbp:treatment |
symptomatic management
|
gptkbp:bfsParent |
gptkb:HDH
|
gptkbp:bfsLayer |
6
|