Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/Bbe40acce999a6a07a88fd0026a50a8b2> ?p ?o ?g. }
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- Bbe40acce999a6a07a88fd0026a50a8b2 hasDbXref "Orphanet:495930" @default.
- Bbe40acce999a6a07a88fd0026a50a8b2 type Axiom @default.
- Bbe40acce999a6a07a88fd0026a50a8b2 annotatedProperty IAO_0000115 @default.
- Bbe40acce999a6a07a88fd0026a50a8b2 annotatedSource MONDO_0044645 @default.
- Bbe40acce999a6a07a88fd0026a50a8b2 annotatedTarget "A rare neoplastic disease characterized by infantile to childhood onset of evidence of bone marrow insufficiency/failure associated with increased risk for myelodysplastic syndrome or acute myeloid leukemia. Most patients present with petechiae, easy bruising, or anemia. Rapid progression is common, and prognosis is generally poor." @default.