WormBase Tree Display for DO_term: DOID:0110714
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| DOID:0110714 | Name | congenital stationary night blindness 1G | |||
|---|---|---|---|---|---|
| Status | Valid | ||||
| 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. | ||||
| Synonym | Exact | CSNB1G | |||
| congenital stationary night blindness type 1G | |||||
| Parent | Is_a | DOID:0050534 | |||
| DOID:0050737 | |||||
| DB_info | Database | OMIM | disease | 616389 | |
| Attribute_of | Gene_by_orthology | WBGene00001666 | |||
| WBGene00001678 |
