OBO ID: DOID:0111793
Term Name: congenital nystagmus 3 Search Ontology:
Synonyms:
  • autosomal dominant congenital nystagmus 3
  • NYS3
Definition: A congenital nystagmus that has_material_basis_in heterozygous mutation in a region of chromosome 7p11.2. https://www.ncbi.nlm.nih.gov/pubmed/9806847
References:
Ontology: Human Disease   ( DOID:0111793 )
OTHER congenital nystagmus 3 PAGES
GENES INVOLVED No data available
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None