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- B8366bbc5e7147f031f2ec4fc1ea499ed hasDbXref "Orphanet:79474" @default.
- B8366bbc5e7147f031f2ec4fc1ea499ed type Axiom @default.
- B8366bbc5e7147f031f2ec4fc1ea499ed annotatedProperty IAO_0000115 @default.
- B8366bbc5e7147f031f2ec4fc1ea499ed annotatedSource MONDO_0019321 @default.
- B8366bbc5e7147f031f2ec4fc1ea499ed annotatedTarget "A heterogeneous group of cases that are clinically diagnosed as Werner syndrome (WS) but do not carry WRN gene mutations. Similar to classical WS caused by WRN mutations, patients generally exhibit an aged appearance and common age-related disorders at earlier ages compared to the general population." @default.