C4303988_SNOMEDCT_US | Knowledge4COVID-19

Property	Value
?:definition	A rare malformation syndrome with multiple congenital abnormalities, described in 2 siblings, with characteristics of VATER-like association in combination with pulmonary hypertension, laryngeal webs, blue sclerae, abnormal ears, persistent growth deficiency and normal intellect.
?:hasCUIAnnotation	<https://research.tib.eu/covid-19/entity/C4303988>
?: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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