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ZIRC
OBO ID: DOID:0110863
Term Name: congenital stationary night blindness autosomal dominant 2 Search Ontology:
Synonyms:
  • CSNBAD2
  • Rambusch type congenital stationary night blindness
Definition: A congenital stationary night blindness characterized by autosomal dominant inhertance that has_material_basis_in heterozygous mutation in the PDE6B gene on chromosome 4p16. https://www.ncbi.nlm.nih.gov/pubmed/8075643
References:
Ontology: Human Disease   (DOID:0110863)
OTHER congenital stationary night blindness autosomal dominant 2 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
PDE6B Night blindness, congenital stationary, autosomal dominant 2 163500
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None