Search Ontology:
Human Disease

congenital nystagmus 3

Term ID
DOID:0111793
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 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models