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
Genes Involved
Zebrafish Models