ZFIN Human Disease: congenital stationary night blindness 1F

OBO ID: DOID:0110864

Term Name:	congenital stationary night blindness 1F		Search Ontology:
Synonyms:	congenital stationary night blindness 1F autosomal recessive CSNB1F
Definition:	A congenital stationary night blindness characterized by autosomal recessive inheritance that has_material_basis_in compound heterozygous mutation in the LRIT3 gene on chromosome 4q25. https://www.ncbi.nlm.nih.gov/pubmed/23246293
References:	OMIM:615058
Ontology:	Human Disease ( DOID:0110864 )

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 1F PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
LRIT3	lrit3b lrit3a	Night blindness, congenital stationary (complete), 1F, autosomal recessive	615058

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None