Term Name: | congenital stationary night blindness 1B |
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Synonyms: | autosomal recessive complete congenital stationary night blindness, congenital stationary night blindness 1B autosomal recessive, CSNB1B |
Definition: | A congenital stationary night blindness characterized by autosomal recessive inheritance that has_material_basis_in mutation in the GRM6 gene on chromosome 5q35. |
Ontology: | Human Disease [DOID:0110865] ( DOID:0110865 ) |