Statements (18)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
gptkb:neurological_disorder
gptkb:disease |
| gptkbp:affects |
children
eye movement |
| gptkbp:firstDescribed |
gptkb:David_G._Cogan
1952 |
| gptkbp:ICD-10_code |
H51.8
|
| gptkbp:inheritance |
autosomal recessive
|
| gptkbp:OMIM |
257550
|
| gptkbp:prevalence |
rare
|
| gptkbp:symptom |
head thrusts to compensate for eye movement
delayed saccades difficulty initiating horizontal eye movements |
| gptkbp:synonym |
congenital oculomotor apraxia
|
| gptkbp:treatment |
supportive therapy
|
| gptkbp:bfsParent |
gptkb:oculomotor_apraxia
|
| gptkbp:bfsLayer |
8
|
| https://www.w3.org/2000/01/rdf-schema#label |
Cogan's oculomotor apraxia
|