Search Ontology:
Human Disease

congenital stationary night blindness 1A

Term ID
DOID:0110870
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 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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