C0311338_SNOMEDCT_US | Knowledge4COVID-19

Property	Value
?:definition	A rare genetic retinal dystrophy with characteristics of the presence of numerous small, round, yellowish-white retinal lesions that are distributed throughout the retina but spare the fovea. Patients present in childhood with non-progressive night blindness with prolonged cone and rod adaptation times. The macula may or may not be involved, which may result in a decrease of central visual acuity with age.
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?:type	<https://research.tib.eu/covid-19/vocab/AnnotationDefinition>

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