Metadata | |
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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 | |
Synonyms |
autosomal recessive complete congenital stationary night blindness [EXACT] congenital stationary night blindness 1B autosomal recessive [EXACT] CSNB1B [EXACT] |
Parent Relationships |