congenital stationary night blindness
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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Summary
congenital stationary night blindness is a class of disease[1]. It is known by 3 alternative names across languages and contexts.[2]
Key Facts
- congenital stationary night blindness's instance of is recorded as class of disease[3].
- congenital stationary night blindness is a type of hereditary night blindness[4].
- congenital stationary night blindness's ICD-9-CM is recorded as 368.61[5].
- congenital stationary night blindness's health specialty is recorded as neurology[6].
- congenital stationary night blindness's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0050534[7].
- congenital stationary night blindness's exact match is recorded as http://identifiers.org/doid/DOID:0050534[8].
- congenital stationary night blindness's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_215[9].
- congenital stationary night blindness's on focus list of Wikimedia project is recorded as WikiProject Medicine[10].
Why It Matters
congenital stationary night blindness is known by 3 alternative names across languages and contexts.[2]