ZFIN Human Disease: congenital stationary night blindness 1D

OBO ID: DOID:0110868

Term Name:	congenital stationary night blindness 1D		Search Ontology:
Synonyms:	congenital stationary night blindness 1D autosomal recessive CSNB1D
Definition:	A congenital stationary night blindness characterized by autosomal recessive inheritance that has_material_basis_in homozygous mutation in the SLC24A1 gene on chromosome 15q22. https://www.ncbi.nlm.nih.gov/pubmed/20850105
References:	OMIM:613830
Ontology:	Human Disease ( DOID:0110868 )

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 1D PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
SLC24A1	slc24a1	Night blindness, congenital stationary (complete), 1D, autosomal recessive	613830

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None