C2931509_SNOMEDCT_US | Knowledge4COVID-19

Property	Value
?:definition	An extremely rare syndrome with characteristics of multiple unerupted permanent teeth, hypoplasia of the alveolar process and of the maxillo-zygomatic region, severe genu valgum and deformed ears. Consanguinity in the family suggested autosomal recessive inheritance.
?:hasCUIAnnotation	<https://research.tib.eu/covid-19/entity/C2931509>
?: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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