Search Ontology:
Human Disease

congenital nystagmus 2

Term ID
DOID:0111792
Synonyms
  • autosomal dominant congenital nystagmus 2
  • congenital motor nystagmus 2
  • NYS2
Definition
A congenital nystagmus that has_material_basis_in heterozygous mutation in a region of chromosome 6p12. https://www.ncbi.nlm.nih.gov/pubmed/8661013
References
Ontology
Human Disease   ( DOID:0111792 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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.