C4750772_SNOMEDCT_US | Knowledge4COVID-19

Property	Value
?:definition	A rare genetic central nervous system malformation syndrome with characteristics of marked prenatal-onset microcephaly, severe motor delay with hypotonia, bilateral polymicrogyria, corpus callosum agenesis, ventricular dilation, small cerebellum and early lethality.
?:hasCUIAnnotation	<https://research.tib.eu/covid-19/entity/C4750772>
?:hasGeneratedBy	<https://research.tib.eu/covid-19/SourceName/SNOMEDCT_US>
?:type	<https://research.tib.eu/covid-19/vocab/AnnotationDefinition>

Metadata

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Anon_0

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Anon_1 (more)

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