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- B545c3f071242a47df9f02b00a493769f hasDbXref "Orphanet:567" @default.
- B545c3f071242a47df9f02b00a493769f type Axiom @default.
- B545c3f071242a47df9f02b00a493769f annotatedProperty IAO_0000115 @default.
- B545c3f071242a47df9f02b00a493769f annotatedSource MONDO_0018923 @default.
- B545c3f071242a47df9f02b00a493769f annotatedTarget "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." @default.