Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B89b7967f447ea2a4887efce9683d452a> ?p ?o ?g. }
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- B89b7967f447ea2a4887efce9683d452a hasDbXref "Orphanet:567" @default.
- B89b7967f447ea2a4887efce9683d452a type Axiom @default.
- B89b7967f447ea2a4887efce9683d452a annotatedProperty IAO_0000115 @default.
- B89b7967f447ea2a4887efce9683d452a annotatedSource MONDO_0018923 @default.
- B89b7967f447ea2a4887efce9683d452a 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.