C0268354_SNOMEDCT_US | Knowledge4COVID-19

Property	Value
?:definition	A syndrome with characteristics of facial dysmorphism, a progeroid appearance, large and late closing fontanelle, cutis laxa, joint hyperlaxity, athetoid movements and hyperreflexia, pre and postnatal growth retardation, intellectual deficit and developmental delay, and corneal clouding and cataract.
?:hasCUIAnnotation	<https://research.tib.eu/covid-19/entity/C0268354>
?: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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