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DOID:0110863 - congenital stationary night blindness autosomal dominant 2
Disease Ontology 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.
Synonyms: CSNBAD2, Rambusch type congenital stationary night blindness,
Xenbase Genes
:
pde6b
| MONDO:0008099 - congenital stationary night blindness autosomal dominant 2 |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
congenital stationary night blindness (is_a)