OBO ID: DOID:0111792
Term Name: congenital nystagmus 2 Search Ontology:
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 )
OTHER congenital nystagmus 2 PAGES
GENES INVOLVED No data available
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None