Extrarenal Rhabdoid Tumor of the Ovary

Preferred Label : Extrarenal Rhabdoid Tumor of the Ovary;

NCIt definition : An extrarenal rhabdoid tumor affecting the ovary.;

Neoplastic status : Malignant;

NCI Metathesaurus CUI : CL1405391;

Details

Origin ID

C171169;

UMLS CUI

C5419027;

Disease may have findings
- Aggressive Clinical Course [NCIt concept]
- High Mitotic Activity [NCIt concept]
- Loss of INI 1 Protein Expression [NCIt concept]
- Necrotic Change [NCIt concept]
Excludes anatomical site(s)
- Bone [NCIt concept]
- Brain [NCIt concept]
- Kidney [NCIt concept]
Has associated anatomic sites
- Adnexa [NCIt concept]
- Connective and Soft Tissue [NCIt concept]
- Female Reproductive System [NCIt concept]
- Genitourinary System [NCIt concept]
- Ovary [NCIt concept]
- Reproductive System [NCIt concept]
- Soft Tissue [NCIt concept]
- Uterine Adnexa [NCIt concept]
Semantic type(s)
- Neoplastic Process [UMLS semantic type]
disease_excludes_finding
- Benign Cellular Infiltrate [NCIt concept]
- Indolent Clinical Course [NCIt concept]
disease_excludes_normal_tissue_origin
- Germinal Layer [NCIt concept]
disease_has_abnormal_cell
- Malignant Cell [NCIt concept]
- Malignant Cell with Large Nucleus and Abundant Eosinophilic Cytoplasm [NCIt concept]
- Neoplastic Cell [NCIt concept]
disease_has_finding
- Childhood Lesion [NCIt concept]
- Intermediate Filaments Present [NCIt concept]
- Intracytoplasmic Eosinophilic Inclusion [NCIt concept]
- Malignant Cellular Infiltrate [NCIt concept]
- Metastatic/Recurrent Disease [NCIt concept]
- Tissue Differentiation Uncertain [NCIt concept]
disease_has_grade
- Grade 4 [NCIt concept]
disease_has_normal_cell_origin
- Embryonic Cell [NCIt concept]
disease_has_normal_tissue_origin
- Embryonic Tissue [NCIt concept]
disease_has_primary_anatomic_site
- Ovary [NCIt concept]
- Soft Tissue [NCIt concept]
disease_mapped_to_gene
- SMARCB1 Gene [NCIt concept]
disease_may_have_abnormal_cell
- Non-Neoplastic Osteoclast-Like Giant Cell [NCIt concept]
disease_may_have_cytogenetic_abnormality
- Loss of Chromosome 22 [NCIt concept]
disease_may_have_molecular_abnormality
- SMARCB1 Gene Mutation [NCIt concept]

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