ZFIN Human Disease: congenital stationary night blindness autosomal dominant 2

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:	OMIM:163500
Ontology:	Human Disease ( DOID:0110863 )

Relationships

is a type of:	autosomal dominant disease congenital stationary night blindness autosomal dominant disease congenital stationary night blindness Show first 5 Terms

OTHER congenital stationary night blindness autosomal dominant 2 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
PDE6B	pde6b	Night blindness, congenital stationary, autosomal dominant 2	163500

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None