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- B381e9fdaefe02d42144c0c90a43ac16e hasDbXref "Orphanet:488280" @default.
- B381e9fdaefe02d42144c0c90a43ac16e type Axiom @default.
- B381e9fdaefe02d42144c0c90a43ac16e annotatedProperty IAO_0000115 @default.
- B381e9fdaefe02d42144c0c90a43ac16e annotatedSource MONDO_0014707 @default.
- B381e9fdaefe02d42144c0c90a43ac16e annotatedTarget "14q32 duplication syndrome is a rare chromosomal anomaly syndrome resulting from the partial duplication of the long arm of chromosome 14 that results in a predisposition to a number of adult-onset myeloproliferative neoplasms, including acute myeloid leukemia, chronic myelomonocytic leukemia, and myeloproliferative neoplasms, especially essential thrombocythemia. Progression to myelofibrosis and secondary acute myeloid leukemia can be observed." @default.