| Metadata | |
|---|---|
| ID | DOID:0110714 |
| Name | congenital stationary night blindness 1G |
| Definition | A congenital stationary night blindness characterized by autosomal recessive inheritance that has_material_basis_in homozygous mutation in the GNAT1 gene on chromosome 3p21. https://www.ncbi.nlm.nih.gov/pubmed/22190596 |
| Xrefs | |
| Synonyms |
congenital stationary night blindness type 1G [EXACT] CSNB1G [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 |