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inflammatory myofibroblastic tumor

Disease Summary
Associated Targets (7)
Tbio

5

Tclin

1

Tchem

1


GARD Rare
Mondo Description A multinodular intermediate fibroblastic neoplasm that arises from soft tissue or viscera, in children and young adults. It is characterized by the presence of spindle-shaped fibroblasts and myofibroblasts, and a chronic inflammatory infiltrate composed of eosinophils, lymphocytes, and plasma cells.
Disease Ontology Description A mesenchymal cell neoplasm that has_material_basis_in myofibroblastic cells admixed with inflammatory cells.
Mondo Term and Equivalent IDs
MONDO:0015798:  inflammatory myofibroblastic tumor
GARD:0007146: 
MESH:D006104: 
NCIT:C6481: 
ONCOTREE:IMT: 
Orphanet:178342: 
UMLS:C0334121: