Search Ontology:
Human Disease

congenital nystagmus 1

Term ID
DOID:0111790
Synonyms
  • congenital motor nystagmus 1
  • NYS1
  • X-linked infantile nystagmus 1
Definition
A congenital nystagmus that has_material_basis_in mutation in the FRMD7 gene on chromosome Xq26.2. https://www.ncbi.nlm.nih.gov/pubmed/17013395
References
Ontology
Human Disease   ( DOID:0111790 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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