Search Ontology:
Human Disease

congenital nystagmus 7

Term ID
DOID:0111791
Synonyms
  • autosomal dominant congenital nystagmus 7
  • NYS7
Definition
A congenital nystagmus that has_material_basis_in heterozygous mutation in a region of chromosome 1q31.3-q32.1. https://www.ncbi.nlm.nih.gov/pubmed/22065086
References
Ontology
Human Disease   ( DOID:0111791 )
Relationships
is a type of
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Genes Involved
Zebrafish Models
Citations