Search Ontology:
Human Disease

congenital nystagmus 5

Term ID
DOID:0111796
Synonyms
  • NYS5
  • X-linked congenital nystagmus 5
Definition
A congenital nystagmus that has_material_basis_in hemizygous or heterozygous mutation in a region of chromosome Xp11.4. https://www.ncbi.nlm.nih.gov/pubmed/10090899
References
Ontology
Human Disease   ( DOID:0111796 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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