Search Ontology:
Human Disease
ocular motor apraxia, Cogan type
- Term ID
- DOID:0080849
- Synonyms
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- 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
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- GARD:16
- MIM:257550
- ORDO:1404
- Ontology
- Human Disease ( DOID:0080849 )
- is a type of
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Genes Involved
Zebrafish Models