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DiGeorge syndrome
? TBD
Medical condition caused by chromosomal abnormality
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DiGeorge syndrome, also known as 22q11.2 deletion syndrome, is a genetic disorder caused by a microdeletion on the long arm of chromosome 22. While the symptoms can vary, they often include congenital heart problems, specific facial features, frequent infections, developmental disability, intellectual disability and cleft palate. Associated...

Instance of
designated intractable/rare disease
Rare disease
class of disease
Subclass of
Syndrome
autosomal dominant disease
Disease
Wikidata