OBO ID: DOID:0111791
Term Name: congenital nystagmus 7 Search Ontology:
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:
OTHER congenital nystagmus 7 PAGES
GENES INVOLVED No data available
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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