Search Ontology:
Human Disease

congenital stationary night blindness autosomal dominant 2

Term ID
DOID:0110863
Synonyms
  • CSNBAD2
  • Rambusch type congenital stationary night blindness
Definition
A congenital stationary night blindness characterized by autosomal dominant inheritance 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 )
Relationships
is a type of
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Genes Involved
Zebrafish Models