OBO ID: DOID:0111790
Term Name: congenital nystagmus 1 Search Ontology:
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 congenital nystagmus 1 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
FRMD7 Nystagmus 1, congenital, X-linked 310700
Nystagmus, infantile periodic alternating, X-linked 310700
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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