congenital nervous system disorder immune system disorder heart disorder multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome obsolete syndromic anorectal malformation 22q11.2 deletion syndrome https://github.com/monarch-initiative/mondo/issues/3664 https://github.com/monarch-initiative/mondo/issues/6747 22q11DS MONDO:0018923 conotruncal anomaly face syndrome DiGeorge syndrome Shprintzen syndrome monosomy 22q11 DECIPHER:16 NORD:853 Chromosome 22q11.2 Deletion Syndrome Orphanet:567 Takao syndrome NANDO:1200339 Sedlackova syndrome icd11.foundation:1868156761 DiGeorge sequence microdeletion 22q11.2 MedDRA:10012979 GARD:0010299 VCFS catch 22 NANDO:2200712 Cayler cardiofacial syndrome NANDO:1200688 MedDRA:10066430 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. chromosome 22q deletion obsolete_22q11.2 deletion syndrome