| 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 | |
| Synonyms |
autosomal recessive complete congenital stationary night blindness [EXACT] congenital stationary night blindness 1B autosomal recessive [EXACT] CSNB1B [EXACT] |
| Parent Relationships | |
| Subclass Logical Relationships |
has material basis in some autosomal recessive inheritance disease has basis in some Abnormality of prenatal development or birth |