DISEASES

Disease-gene associations mined from literature

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Human genes for myeloproliferative disorder with eosinophilia

Myeloproliferative disorder with eosinophilia [DOID:0111344]

A myeloproliferative neoplasm characterized by chronic proliferation of myeloid cells and eosinophilia in the peripheral blood and bone marrow that has_material_basis_in a fusion of ETV6 and PDGFRB formed by a translocation from chromosome 12 to chromosome 5q32.

Synonyms:  myeloproliferative disorder with eosinophilia,  DOID:0111344,  myeloproliferative disorder with eosinophilias,  chronic myeloproliferative disorder with eosinophilia,  chronic myeloproliferative disorder with eosinophilias

The disease-gene associations are derived from automatic text mining of the biomedical literature, manually curated database annotations, cancer mutation data, and genome-wide association studies. The confidence of each association is signified by stars, where ★★★★★ is the highest confidence and ★☆☆☆☆ is the lowest.

Developed by Sune Frankild, Alexander Junge, Albert Pallejà, Dhouha Grissa, Kalliopi Tsafou, and Lars Juhl Jensen from the Novo Nordisk Foundation Center for Protein Research.