ZFIN Human Disease: Oguchi disease-2

OBO ID: DOID:0110713

Term Name:	Oguchi disease-2		Search Ontology:
Synonyms:	congenital stationary night blindness Oguchi type 2 CSNBO2
Definition:	A congenital stationary night blindness characterized by congenital static night blindness, a golden or gray-white discoloration of the fundus that disappears in the dark-adapted state and typically normal function of all other visual functions that has_material_basis_in homozygous mutation in the GRK1 gene on chromosome 13q34. (2)
References:	OMIM:613411
Ontology:	Human Disease ( DOID:0110713 )

Relationships

is a type of:	autosomal recessive disease congenital stationary night blindness autosomal recessive disease congenital stationary night blindness Show first 5 Terms
inverse disjoint_from:	Oguchi disease-1 Oguchi disease-1 Show first 5 Terms

OTHER Oguchi disease-2 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
GRK1	grk1a	Oguchi disease-2	613411

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None