Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B1b77eb0c4a9b47311a2d49d2c0fc7f6c> ?p ?o ?g. }
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- B1b77eb0c4a9b47311a2d49d2c0fc7f6c hasDbXref "Orphanet:168950" @default.
- B1b77eb0c4a9b47311a2d49d2c0fc7f6c type Axiom @default.
- B1b77eb0c4a9b47311a2d49d2c0fc7f6c annotatedProperty IAO_0000115 @default.
- B1b77eb0c4a9b47311a2d49d2c0fc7f6c annotatedSource MONDO_0015690 @default.
- B1b77eb0c4a9b47311a2d49d2c0fc7f6c annotatedTarget "A rare, malignant, neoplastic disease characterized by clonal proliferation of myeloid and/or lymphoid precursors harboring rearrangements in the PDGFRB gene, in the blood, bone marrow and often other tissues as well (spleen, lymph nodes, skin, etc.). It usually presents as chronic myelomonocytic leukemia with eosinophilia, chronic eosinophilic leukemia, atypical chronic myelogenous leukemia, juvenile myelomonocytic leukemia, myelodysplastic syndrome, acute myeloid leukemia or acute lymphoblastic leukemia. Patients usually present with anemia, leukocytosis, monocytosis, eosinophilia and/or splenomegaly, or systemic symptoms, such as fever, sweating and/or weight loss." @default.