ZFIN Human Disease: congenital stationary night blindness 1B

OBO ID: DOID:0110865

Term Name:	congenital stationary night blindness 1B		Search Ontology:
Synonyms:	autosomal recessive complete congenital stationary night blindness congenital stationary night blindness 1B autosomal recessive CSNB1B
Definition:	A congenital stationary night blindness characterized by autosomal recessive inheritance that has_material_basis_in mutation in the GRM6 gene on chromosome 5q35. https://www.ncbi.nlm.nih.gov/pubmed/15781871
References:	OMIM:257270
Ontology:	Human Disease ( DOID:0110865 )

Relationships

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

OTHER congenital stationary night blindness 1B PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
GRM6	grm6a grm6b	Night blindness, congenital stationary (complete), 1B, autosomal recessive	257270

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None