Outbound Relationships |
Type |
Target |
Active |
Characteristic |
Refinability |
Group |
Values |
Chorea due to Huntington disease-like 1 (disorder) |
Is a |
Chorea co-occurrent and due to Huntington disease-like condition (disorder) |
true |
Inferred relationship |
Some |
|
|
Chorea due to Huntington disease-like 1 (disorder) |
Interprets |
mouvement |
false |
Inferred relationship |
Some |
1 |
|
Chorea due to Huntington disease-like 1 (disorder) |
Due to |
A rare, genetic, human prion disease characterized by adult-onset neurodegenerative manifestations associated with a movement disorder and psychiatric/behavioral disturbances. Patients typically present personality changes, aggressiveness, manias, anxiety and/or depression in conjunction with rapidly progressive cognitive decline (presenting with dysarthria, apraxia, aphasia, and eventually leading to dementia) as well as ataxia (manifesting with gait disturbances, unsteadiness, coordination problems), Parkinsonism, myoclonus, and/or chorea. Additional features may include generalized spasticity, seizures, urine incontinence and pyramidal abnormalities. |
true |
Inferred relationship |
Some |
2 |
|
Chorea due to Huntington disease-like 1 (disorder) |
Finding site |
Structure of basal nucleus |
true |
Inferred relationship |
Some |
3 |
|
Chorea due to Huntington disease-like 1 (disorder) |
Is a |
Chorea due to heredodegenerative disorder |
true |
Inferred relationship |
Some |
|
|
Chorea due to Huntington disease-like 1 (disorder) |
Interprets |
Movement observable |
true |
Inferred relationship |
Some |
4 |
|
Chorea due to Huntington disease-like 1 (disorder) |
Has interpretation |
Abnormal |
true |
Inferred relationship |
Some |
4 |
|