Visualize Submit Comment
Metadata
ID DOID:0110868
Name congenital stationary night blindness 1D
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
Xrefs

OMIM:613830

Synonyms

congenital stationary night blindness 1D autosomal recessive [EXACT]

CSNB1D [EXACT]

Parent Relationships

is_a congenital stationary night blindness

Add an item to the term tracker