Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0206142
Disease: Eosinophilic leukemia
Eosinophilic leukemia
0.330 Biomarker disease BEFREE Here, we present a collection of 2,6,9-trisubstituted purines with nanomolar potency against PDGFRα and strong and selective cytotoxicity in the human eosinophilic leukaemia cell line EOL-1 that expresses the FIP1L1-PDGFRA oncogene. 31514019 2019
CUI: C0206142
Disease: Eosinophilic leukemia
Eosinophilic leukemia
0.330 Biomarker disease CTD_human Hypereosinophilic Syndrome as a Rare Cause of Reversible Biventricular Heart Failure. 28347583 2017
CUI: C0206142
Disease: Eosinophilic leukemia
Eosinophilic leukemia
0.330 GeneticVariation disease BEFREE Most notably, chromosomal rearrangements, such as FIP1L1-PDGFRA fusions caused by internal deletions in chromosome 4, are now known to be associated with many chronic eosinophilic leukemias. 23368869 2013
CUI: C0206142
Disease: Eosinophilic leukemia
Eosinophilic leukemia
0.330 Biomarker disease CTD_human Apoptosis induction by retinoids in eosinophilic leukemia cells: implication of retinoic acid receptor-alpha signaling in all-trans-retinoic acid hypersensitivity. 16778211 2006
CUI: C0206142
Disease: Eosinophilic leukemia
Eosinophilic leukemia
0.330 GeneticVariation disease BEFREE The FIP1L1-PDGFRA fusion gene is generated by a cryptic interstitial chromosomal deletion, del(4)(q12q12), which indicates that these cases are clonal hematopoietic malignancies and should be reclassified as chronic eosinophilic leukemias based on current World Health Organization recommendations. 14676627 2004