WormBase Tree Display for DO_term: DOID:0050534
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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 (2) | ||
Child | Is (14) | ||
Attribute_of | Gene_by_orthology | WBGene00001187 | |
WBGene00001651 | |||
WBGene00001795 | |||
WBGene00001796 | |||
WBGene00003838 | |||
WBGene00003839 | |||
WBGene00003841 | |||
WBGene00003889 |