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Metadata
ID DOID:0110865
Name congenital stationary night blindness 1B
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
Xrefs

OMIM:257270

Synonyms

autosomal recessive complete congenital stationary night blindness [EXACT]

congenital stationary night blindness 1B autosomal recessive [EXACT]

CSNB1B [EXACT]

Parent Relationships

is_a congenital stationary night blindness

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