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ZIRC
OBO ID: DOID:0110870
Term Name: congenital stationary night blindness 1A Search Ontology:
Synonyms:
  • complete CSNB X-linked
  • congenital stationary night blindness 1A X-linked
  • congenital stationary night blindness with myopia
  • CSNB1A
  • hemeralopia-myopia
  • myopia-night blindness
  • NBMI
Definition: A congenital stationary night blindness that has_material_basis_in mutation in the NYX gene on chromosome Xp11.4. https://www.ncbi.nlm.nih.gov/pubmed/9662400
References:
Ontology: Human Disease   (DOID:0110870)
OTHER congenital stationary night blindness 1A PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
NYX Night blindness, congenital stationary (complete), 1A, X-linked 310500
ZEBRAFISH MODELS
Fish Conditions Citations
WT + MO1-nyx standard conditions Peachey et al., 2012
PHENOTYPE No data available

CITATIONS (1)