|
gptkbp:instanceOf
|
gptkb:disease
neurological disorder
|
|
gptkbp:affects
|
gptkb:cerebellum
|
|
gptkbp:associatedWith
|
gptkb:SNX14
gptkb:TOE1
gptkb:VLDLR
|
|
gptkbp:category
|
neurodegenerative disease
genetic disorder
animal disease
|
|
gptkbp:cause
|
degeneration of Purkinje cells
|
|
gptkbp:diagnosedBy
|
neurological examination
MRI
histopathology
|
|
gptkbp:firstDescribed
|
1960s
|
|
gptkbp:hasNoCure
|
true
|
|
https://www.w3.org/2000/01/rdf-schema#label
|
Cerebellar Abiotrophy
|
|
gptkbp:inheritance
|
autosomal recessive
|
|
gptkbp:isHereditary
|
true
|
|
gptkbp:notableInBreed
|
gptkb:dog
gptkb:horse_race
gptkb:Bernese_Mountain_Dog
gptkb:Labrador_Retriever
gptkb:Samoyed
gptkb:Australian_Kelpie
gptkb:American_Staffordshire_Terrier
gptkb:Kerry_Blue_Terrier
gptkb:Miniature_Poodle
|
|
gptkbp:occurredIn
|
gptkb:dog
gptkb:livestock
humans
cats
horses
|
|
gptkbp:onset
|
congenital
juvenile
|
|
gptkbp:progression
|
progressive
|
|
gptkbp:relatedTo
|
gptkb:cerebellar_hypoplasia
|
|
gptkbp:symptom
|
gptkb:hypermetria
ataxia
lack of coordination
head tremors
intention tremor
wide-based stance
|
|
gptkbp:treatment
|
supportive care
|
|
gptkbp:bfsParent
|
gptkb:Arabian
|
|
gptkbp:bfsLayer
|
6
|