congenital stationary night blindness
(Q18553290)
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
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
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Current Data About
congenital stationary night blindness
| (P31) |
(Q112193867)
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| (P279) |
(Q18557952)
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| (P1692) |
368.61
|
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| (P1995) |
(Q83042)
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| (P2888) |
http://purl.obolibrary.org/obo/DOID_0050534
http://identifiers.org/doid/DOID:0050534
http://www.orpha.net/ORDO/Orphanet_215 |
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| (P5008) |
(Q4099686)
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other details
| aliases |
congenital essential nyctalopia |
| description | 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 |
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