Statements (19)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
neurological disorder
|
| gptkbp:affects |
eye movement
|
| gptkbp:alsoKnownAs |
gptkb:Cogan's_oculomotor_apraxia
|
| gptkbp:associatedWith |
ataxia
developmental delay chorea |
| gptkbp:diagnosedBy |
clinical examination
|
| gptkbp:firstDescribed |
gptkb:David_Glendenning_Cogan
1952 |
| https://www.w3.org/2000/01/rdf-schema#label |
oculomotor apraxia
|
| gptkbp:ICD-10_code |
H51.8
|
| gptkbp:inheritance |
autosomal dominant
autosomal recessive |
| gptkbp:subspecies |
Aphasia
|
| gptkbp:symptom |
difficulty moving eyes horizontally
head thrusts to compensate for eye movement |
| gptkbp:treatment |
supportive care
|
| gptkbp:bfsParent |
gptkb:Type_3_Gaucher's_disease
|
| gptkbp:bfsLayer |
6
|