Search Ontology:
Human Disease

congenital nystagmus 6

Term ID
DOID:0111795
Synonyms
  • NYS6
  • X-linked congenital nystagmus 6
Definition
A congenital nystagmus that has_material_basis_in hemizygous of homoxygous mutation in the GPR143 gene on chromosome Xp22.2. https://www.ncbi.nlm.nih.gov/pubmed/17516023
References
Ontology
Human Disease   ( DOID:0111795 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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