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Diseases

Genetic and Rare Diseases Information Center (GARD)

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22q11.2 deletion syndrome


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Other Names for 22q11.2 deletion syndrome

  • Autosomal dominant Opitz G/BBB syndrome
  • CATCH22
  • Cayler cardiofacial syndrome
  • Chromosome 22q11.2 deletion syndrome
  • Conotruncal anomaly face syndrome
  • DiGeorge syndrome
  • Sedlackova syndrome
  • Shprintzen syndrome
  • VCFS
  • Velocardiofacial syndrome