Ewing Sarcoma (ES)

Alias:

Neuroepithelioma

Primitive Neuroectodermal Tumor

Peripheral Neuroepithelioma

Ewings Sarcoma

Ewing's Tumor

Localized Peripheral Primitive Neuroectodermal Tumor

Ewings Sarcoma-Primitive Neuroectodermal Tumor

Peripheral Primitive Neuroectodermal Tumor

Extraskeletal Ewing Sarcoma

Extraosseous Ewing Tumor

Ewing's Sarcoma

Askin Tumor

Localized Ewing's Sarcoma/peripheral Primitive Neuroectodermal Tumor

Extraosseous Ewings Sarcoma-Primitive Neuroepithelial Tumor

Ewing's Sarcoma/peripheral Primitive Neuroectodermal Tumor

Neuroectodermal Tumors, Primitive, Peripheral

Neuroectodermal Tumor, Primitive

Pnet of Thoracopulmonary Region

Ewing's Family Localized Tumor

Ewing Sarcoma Family of Tumors

Neuroepithelioma, Peripheral

Extraosseous Ewing Sarcoma

Localized Ewing's Sarcoma

Tumor of the Ewing Family

Extraskeletal Ewing Tumor

Localized Ewing Sarcoma

Localized Ewing's Tumor

Ewing Family of Tumors

Pnet of the Chest Wall

Sarcoma, Ewing's

Peripheral Pnet

Disorder of Eye

Sarcoma, Ewing

Askin's Tumor

Ewing Tumor

Ppnet

Pnet

Esft

Eoe

Pne

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Ewing Sarcoma, also known as neuroepithelioma, is related to skeletal ewing sarcoma and extraosseous ewing sarcoma, and has symptoms including eye manifestations, pain in or around eye and redness or discharge of eye. An important gene associated with Ewing Sarcoma is EWSR1 (EWS RNA Binding Protein 1), and among its related pathways/superpathways are Chromatin Regulation / Acetylation and Mesenchymal Stem Cells and Lineage-specific Markers. The drugs Dactinomycin and Zoledronic acid have been mentioned in the context of this disorder. Affiliated tissues include bone and bone marrow, and related phenotypes are peripheral primitive neuroectodermal neoplasm and seizure

Related ID：

MALACARDS：EWN003

OMIM：612219

MESH：C563168