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- B045f7b1d14c1b1b5fbb4cda0ad667410 hasDbXref "OMIM:617941" @default.
- B045f7b1d14c1b1b5fbb4cda0ad667410 type Axiom @default.
- B045f7b1d14c1b1b5fbb4cda0ad667410 annotatedProperty IAO_0000115 @default.
- B045f7b1d14c1b1b5fbb4cda0ad667410 annotatedSource MONDO_0044205 @default.
- B045f7b1d14c1b1b5fbb4cda0ad667410 annotatedTarget "Shwachman-Diamond syndrome-2 (SDS2) is characterized by exocrine pancreatic dysfunction, hematopoietic abnormalities, short stature, and metaphyseal dysplasia ({1:Stepensky et al., 2017}).nnFor a discussion of genetic heterogeneity of Shwachman-Diamond syndrome, see SDS1 (OMIM:260400)." @default.