(Q525642)

English

DiGeorge syndrome

T cell deficiency disease that is the result of a large deletion of chromosome 22, which includes the DGS gene needed for development of the thymus and related glands with subsequent lack of T-cell production

  • DiGeorge sequence (disorder)
  • DiGeorge's syndrome
  • Pharyngeal pouch syndrome
  • 22q11.2 deletion syndrome
  • DiGeorge sequence

Statements

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DiGeorge syndrome
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Identifiers

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LD44.N0
CATCH 22 phenotype
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digeorge-syndrome
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