Uterine Corpus Inflammatory Myofibroblastic Tumor

Preferred Label : Uterine Corpus Inflammatory Myofibroblastic Tumor;

NCIt definition : A rare inflammatory myofibroblastic tumor that arises from the uterine corpus.;

Neoplastic status : Undetermined;

NCI Metathesaurus CUI : CL1662963;

Détails

Origin ID

C180545;

UMLS CUI

C5556457;

Disease excludes normal cell origin
- Neuron, Neuroepithelial Cell, and Supporting Cell of the Nervous System [NCIt concept]
Disease may have findings
- Fascicular Pattern [NCIt concept]
- Fever [NCIt concept]
- Multinodular Lesion [NCIt concept]
- Myxoid Changes Present [NCIt concept]
- Pain [NCIt concept]
- Well-Circumscribed Lesion [NCIt concept]
Has associated anatomic sites
- Connective and Soft Tissue [NCIt concept]
- Corpus Uteri [NCIt concept]
- Female Reproductive System [NCIt concept]
- Genitourinary System [NCIt concept]
- Reproductive System [NCIt concept]
- Soft Tissue [NCIt concept]
- Uterus [NCIt concept]
Semantic type(s)
- Neoplastic Process [UMLS semantic type]
disease_has_abnormal_cell
- Neoplastic Cell [NCIt concept]
- Neoplastic Connective and Soft Tissue Cell [NCIt concept]
- Neoplastic Fibroblast [NCIt concept]
- Neoplastic Spindle-Shaped Fibroblast [NCIt concept]
- Neoplastic Spindle-Shaped Myofibroblast [NCIt concept]
disease_has_finding
- Eosinophilic Infiltrate [NCIt concept]
- Locally Aggressive Lesion [NCIt concept]
- Lymphocytic Infiltrate [NCIt concept]
- Plasmacytic Infiltrate [NCIt concept]
disease_has_normal_cell_origin
- Connective and Soft Tissue Cell [NCIt concept]
- Fibroblast [NCIt concept]
disease_has_primary_anatomic_site
- Connective and Soft Tissue [NCIt concept]
- Corpus Uteri [NCIt concept]
- Soft Tissue [NCIt concept]
disease_mapped_to_gene
- ALK Gene [NCIt concept]
- CLTC/ALK Fusion Gene [NCIt concept]
- HMGA2 Gene [NCIt concept]
- TPM3/ALK Fusion Gene [NCIt concept]
- TPM4/ALK Fusion Gene [NCIt concept]
disease_may_have_abnormal_cell
- Ganglion-Like Cell [NCIt concept]
- Neoplastic Stellate Cell [NCIt concept]
disease_may_have_cytogenetic_abnormality
- t(1;2)(q25;p23) [NCIt concept]
- t(2;17)(p23;q23) [NCIt concept]
- t(2;19)(p23;p13) [NCIt concept]
disease_may_have_molecular_abnormality
- ALK Gene Rearrangement [NCIt concept]
- CLTC-ALK Fusion Protein Expression [NCIt concept]
- TPM3-ALK Fusion Protein Expression [NCIt concept]
- TPM4-ALK Fusion Protein Expression [NCIt concept]

Position du mot-clé dans l'(les) arborescence(s) :

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