WormBase Tree Display for DO_term: DOID:0050534
expand all nodes | collapse all nodes | view schema
| DOID:0050534 | Name | congenital stationary night blindness | |
|---|---|---|---|
| Status | Valid | ||
| Definition | A hereditary night blindness that is characterized by hemeralopia with a moderate loss of visual acuity and caused by defective photoreceptor-to-bipolar cell signaling with common ERG findings of reduced or absent b-waves and generally normal a-waves. | ||
| Comment | Xref MGI. | ||
| Synonym | Exact | congenital essential nyctalopia | |
| Parent | Is_a | DOID:8498 | |
| DOID:0080015 | |||
| Child | Is (14) | ||
| Attribute_of | Gene_by_orthology | WBGene00001187 | |
| WBGene00001651 | |||
| WBGene00001795 | |||
| WBGene00001796 | |||
| WBGene00003838 | |||
| WBGene00003839 | |||
| WBGene00003841 | |||
| WBGene00003889 |
