C5190512_SNOMEDCT_US | Knowledge4COVID-19

Property	Value
?:definition	A rare chromosomal anomaly with characteristics of variable clinical features that may include developmental delay, mild intellectual disability and dysmorphic facial features. In some cases, microcephaly, growth retardation and congenital heart defects have been reported.
?:hasCUIAnnotation	<https://research.tib.eu/covid-19/entity/C5190512>
?:hasGeneratedBy	<https://research.tib.eu/covid-19/SourceName/SNOMEDCT_US>
?:type	<https://research.tib.eu/covid-19/vocab/AnnotationDefinition>

Metadata

Anon_0

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Anon_0

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Anon_1 (more)

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