22q11.2 deletion syndrome

From BugSigDB


22q11.2 deletion syndrome (DS) is a chromosomal anomaly which causes a congenital malformation disorder whose common features include cardiac defects, palatal anomalies, facial dysmorphism, developmental delay and immune deficiency.
Aliases
  • 22q11.2 deletion syndrome
  • 22q11DS
  • CATCH 22
  • catch 22
  • Cayler cardiofacial syndrome
  • Conotruncal anomaly face syndrome
  • conotruncal anomaly face syndrome
  • DiGeorge sequence
  • DiGeorge syndrome
  • Microdeletion 22q11.2
  • microdeletion 22q11.2
  • Monosomy 22q11
  • monosomy 22q11
  • Sedlackova syndrome
  • Shprintzen syndrome
  • Takao syndrome
  • VCFS
  • Velocardiofacial syndrome
  • velocardiofacial syndrome