Childhood Pseudomyogenic Hemangioendothelioma

Preferred Label : Childhood Pseudomyogenic Hemangioendothelioma;

NCIt synonyms : Pediatric Pseudomyogenic Hemangioendothelioma;

NCIt definition : A pseudomyogenic hemangioendothelioma that occurs during childhood.;

Neoplastic status : Undetermined;

NCI Metathesaurus CUI : CL1793988;

Details

Origin ID

C188979;

UMLS CUI

C5708166;

Disease may have findings
- Multifocal Lesion [NCIt concept]
- Pain [NCIt concept]
- Skin Nodule [NCIt concept]
- Subcutaneous Nodule [NCIt concept]
Excludes anatomical site(s)
- Bone [NCIt concept]
Has associated anatomic sites
- Cardiovascular System [NCIt concept]
- Connective and Soft Tissue [NCIt concept]
- Vascular System [NCIt concept]
Semantic type(s)
- Neoplastic Process [UMLS semantic type]
disease_has_abnormal_cell
- Epithelioid Endothelial Cell [NCIt concept]
- Neoplastic Cell [NCIt concept]
- Neoplastic Endothelial Cell [NCIt concept]
- Spindle Endothelial Cell [NCIt concept]
disease_has_finding
- Childhood Lesion [NCIt concept]
- Locally Aggressive Lesion [NCIt concept]
- Rarely Metastasizing Lesion [NCIt concept]
- Vascular Channel Formation [NCIt concept]
disease_has_normal_cell_origin
- Endothelial Cell [NCIt concept]
disease_has_normal_tissue_origin
- Blood Vessel Endothelium [NCIt concept]
- Soft Tissue [NCIt concept]
- Vascular Endothelium [NCIt concept]
disease_has_primary_anatomic_site
- Blood Vessel [NCIt concept]
- Vascular System [NCIt concept]
disease_mapped_to_gene
- ACTB/FOSB Fusion Gene [NCIt concept]
- CLTC/FOSB Fusion Gene [NCIt concept]
- EGFL7/FOSB Fusion Gene [NCIt concept]
- FOSB Gene [NCIt concept]
- SERPINE1/FOSB Fusion Gene [NCIt concept]
- WWTR1/FOSB Fusion Gene [NCIt concept]
disease_may_have_cytogenetic_abnormality
- FOSB Gene Rearrangement [NCIt concept]
- t(7;19)(q22;q13) [NCIt concept]

Keyword's position in hierarchy(ies) :

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