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
