Statements (21)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
gptkb:neurodegenerative_disease
gptkb:disease |
| gptkbp:alsoKnownAs |
juvenile Huntington's disease
|
| gptkbp:cause |
mutation in HTT gene
|
| gptkbp:field |
genetics
neurology |
| gptkbp:firstDescribed |
1883
|
| gptkbp:ICD-10_code |
G10
|
| gptkbp:inheritance |
autosomal dominant
|
| gptkbp:namedAfter |
gptkb:Ludwig_Pick
Carl Westphal |
| gptkbp:OMIM |
143100
|
| gptkbp:onset |
childhood
adolescence |
| gptkbp:relatedTo |
gptkb:Huntington's_disease
|
| gptkbp:symptom |
gptkb:movement_disorder
cognitive decline psychiatric symptoms |
| gptkbp:bfsParent |
gptkb:Alexander_Westphal
|
| gptkbp:bfsLayer |
8
|
| http://www.w3.org/2000/01/rdf-schema#label |
Westphal–Pick disease
|