myeloid neoplasm associated with FGFR1 rearrangement https://github.com/monarch-initiative/mondo/issues/7614 https://www.malacards.org/card/chromosome_8p11_myeloproliferative_syndrome https://www.malacards.org/card/myeloid_and_lymphoid_neoplasms_associated_with_fgfr1_abnormalities Hematologic neoplasms characterized by the rearrangement of the FGFR1 gene, resulting in translocations with an 8p11 breakpoint. Patients present with a myeloproliferative neoplasm, acute myeloid leukemia, lymphoblastic lymphoma/leukemia of T or B-cell lineage, or acute leukemia of mixed phenotype. myeloid/lymphoid neoplasms with FGFR1 rearrangement MEDGEN:462123 stem cell leukemia/lymphoma ONCOTREE:MLNFGFR1 NCIT:C84277 OMIM:613523 8p11 myeloproliferative syndrome myeloid/lymphoid neoplasm associated with FGFR1 rearrangement chromosome 8p11 myeloproliferative syndrome 8p11 stem cell syndrome DOID:0080167 icd11.foundation:2019647878 myeloid and lymphoid neoplasms with FGFR1 rearrangement UMLS:C3150773 myeloid and lymphoid neoplasms associated with FGFR1 abnormalities 8p11 stem cell leukemia/lymphoma syndrome MONDO:0013296 GARD:0017043 Orphanet:168953 ICDO:9967/3 myeloid/lymphoid neoplasms associated with eosinophilia and abnormality of PDGFRA, PDGFRB, FGFR1 or JAK2