Search Ontology:
Human Disease

ocular motor apraxia, Cogan type

Term ID
DOID:0080849
Synonyms
Definition
An eye disease that is characterized by defective or absent horizontal voluntary eye movements, and defective or absent horizontal ocular attraction movements. (3)
References
Ontology
Human Disease   ( DOID:0080849 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
Citations
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