C0265328_SNOMEDCT_US | Knowledge4COVID-19

Property	Value
?:definition	A rare genetic epilepsy syndrome with characteristics of congenital alopecia, early-onset epilepsy, intellectual disability and speech delay. Large stature, delayed bone development and abnormal electroencephalogram have also been associated.
?:hasCUIAnnotation	<https://research.tib.eu/covid-19/entity/C0265328>
?:hasGeneratedBy	<https://research.tib.eu/covid-19/SourceName/SNOMEDCT_US>
?:type	<https://research.tib.eu/covid-19/vocab/AnnotationDefinition>

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Anon_0

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