Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0026987
Disease: Myelofibrosis
Myelofibrosis
0.900 Biomarker disease BEFREE Conversely, elimination of macrophages expressing MPL by clodronate liposomes reversed the MF phenotype of the murine model, suggesting that fibrocyte differentiation induced by MPL activation contributes to the progression of MF. 28386106 2017
CUI: C0026987
Disease: Myelofibrosis
Myelofibrosis
0.900 GeneticVariation disease BEFREE A 65-year-old woman with MPL-mutated essential thrombocythemia and progression to myelofibrosis was noted upon routine pretransplant testing to have mixed field reactivity with anti-D and an historic discrepancy in RhD type. 28653329 2017
CUI: C0026987
Disease: Myelofibrosis
Myelofibrosis
0.900 Biomarker disease BEFREE Correction: Myeloproliferative leukemia protein activation directly induces fibrocyte differentiation to cause myelofibrosis. 30232464 2018
CUI: C0026987
Disease: Myelofibrosis
Myelofibrosis
0.900 GeneticVariation disease BEFREE Key differences from the 2011 diagnostic recommendations included: lower threshold values for hemoglobin and hematocrit and bone marrow examination for diagnosis of polycythemia vera (PV), according to the revised WHO criteria; the search for complementary clonal markers, such as ASXL1, EZH2, IDH1/IDH2, and SRSF2 for the diagnosis of myelofibrosis (MF) in patients who test negative for JAK2V617, CALR or MPL driver mutations. 29515238 2018
CUI: C0026987
Disease: Myelofibrosis
Myelofibrosis
0.900 GeneticVariation disease BEFREE Only about 10% of patients with myelofibrosis harbor alterations in MPL gene. 31446640 2019
CUI: C0026987
Disease: Myelofibrosis
Myelofibrosis
0.900 GeneticVariation disease BEFREE Whether noncanonical and/or concomitant JAK2- and MPL-mutations exist in myelofibrosis (MF) regardless of phenotype-driver mutations is not yet elucidated. 31135094 2019
CUI: C0026987
Disease: Myelofibrosis
Myelofibrosis
0.900 GeneticVariation disease BEFREE ABSTRACT: Background The BCR-ABL-negative myeloproliferative neoplasms, i.e., polycythemia vera, essential thrombocythemia (ET), and myelofibrosis (MF), are characterized by mutations in JAK2, CALR, or MPL. 30889303 2019
CUI: C0026987
Disease: Myelofibrosis
Myelofibrosis
0.900 GeneticVariation disease BEFREE Immune thrombocytopenia is associated with persistently deranged fibrosis-related seromarker profiles but low bone marrow fibrosis grades: A 2-year observational study on thrombopoietin receptor agonist treatment. 29293383 2019
CUI: C0026987
Disease: Myelofibrosis
Myelofibrosis
0.900 AlteredExpression disease BEFREE The discovery of mutations in JAK2, CALR, and MPL have uncovered activated JAK-STAT signaling as a primary driver of MF, supporting a rationale for JAK inhibition. 31511492 2019
CUI: C0026987
Disease: Myelofibrosis
Myelofibrosis
0.900 GeneticVariation disease BEFREE "Driver" mutations in JAK2, MPL and indels in CALR underlie the vast majority of cases of PMF and post-ET MF; the remainder (≈ 10%) lack identifiable driver mutations, but other clonal markers are usually detectable. 31630335 2020