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- Bc97c9cab347db43c40e88dda740eec7f hasDbXref "Orphanet:48652" @default.
- Bc97c9cab347db43c40e88dda740eec7f type Axiom @default.
- Bc97c9cab347db43c40e88dda740eec7f annotatedProperty IAO_0000115 @default.
- Bc97c9cab347db43c40e88dda740eec7f annotatedSource MONDO_0011652 @default.
- Bc97c9cab347db43c40e88dda740eec7f annotatedTarget "Monosomy 22q13 syndrome (deletion 22q13.3 syndrome or Phelan-McDermid syndrome) is a chromosome microdeletion syndrome characterized by neonatal hypotonia, global developmental delay, normal to accelerated growth, absent to severely delayed speech, and minor dysmorphic features." @default.