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Concept information

Término preferido

DiGeorge syndrome  

Definición

  • DiGeorge syndrome, also known as 22q11.2 deletion syndrome, is a syndrome caused by the deletion of a small segment of chromosome 22. While the symptoms can vary, they often include congenital heart problems, specific facial features, frequent infections, developmental delay, learning problems and cleft palate. (Wikipedia)

etiqueta alternativa (skos)

  • velocardiofacial syndrome

En otras lenguas

URI

http://data.loterre.fr/ark:/67375/VH8-N0JB9FMQ-0

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