Night blindness, congenital stationary, autosomal dominant 2; CSNBAD2

Disease ID:973
Name:Night blindness, congenital stationary, autosomal dominant 2; CSNBAD2
Associated with:1 target
Synonyms
Congenital stationary night blindness
Database Links
Disease Ontology: DOID:0050534
OMIM: 163500
Orphanet: ORPHA215

Targets

phosphodiesterase 6B

Ligands

No ligand related data available for Night blindness, congenital stationary, autosomal dominant 2; CSNBAD2