OBO ID: DOID:0080849
Term Name: ocular motor apraxia, Cogan type Search Ontology:
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 ocular motor apraxia, Cogan type PAGES
GENES INVOLVED No data available
ZEBRAFISH MODELS
Fish Conditions Citations
dscaml1vt1/+; cu2Tg standard conditions Ma 马漫修 et al., 2019
PHENOTYPE No data available

CITATIONS (1)
Your Input Welcome
We welcome your input and comments. Please use this form to recommend updates to the information in ZFIN. We appreciate as much detail as possible and references as appropriate. We will review your comments promptly.
Please check the highlighted fields and try again.
Thank you for submitting comments. Your input has been emailed to ZFIN curators who may contact you if additional information is required.
Oops. Something went wrong. Please try again later.