Unresectable Peritoneal Sarcomatoid Mesothelioma

Preferred Label : Unresectable Peritoneal Sarcomatoid Mesothelioma;

NCIt definition : Peritoneal sarcomatoid mesothelioma that is not amenable to surgical resection.;

Neoplastic status : Malignant;

NCI Metathesaurus CUI : CL1407341;

Details

Origin ID

C173614;

UMLS CUI

C5420305;

Disease may have findings
- Abdominal Pain [NCIt concept]
- Anaplastic Lesion [NCIt concept]
- Peritoneal Effusion [NCIt concept]
Has associated anatomic sites
- Peritoneal Cavity [NCIt concept]
- Peritoneum [NCIt concept]
- Peritoneum and Retroperitoneum [NCIt concept]
Semantic type(s)
- Neoplastic Process [UMLS semantic type]
concept_is_in_subset
- CTRP Disease Terminology [NCIt concept]
- CTRP Terminology [NCIt concept]
disease_excludes_finding
- Benign Cellular Infiltrate [NCIt concept]
disease_has_abnormal_cell
- Malignant Cell [NCIt concept]
- Malignant Mesothelial Cell [NCIt concept]
- Malignant Spindle Mesothelial Cell [NCIt concept]
- Neoplastic Cell [NCIt concept]
- Neoplastic Mesothelial Cell [NCIt concept]
disease_has_finding
- Diffuse Pattern [NCIt concept]
- Malignant Cellular Infiltrate [NCIt concept]
- Unresectable Mass [NCIt concept]
disease_has_normal_cell_origin
- Mesothelial Cell [NCIt concept]
disease_has_normal_tissue_origin
- Mesothelium [NCIt concept]
- Peritoneum [NCIt concept]
disease_has_primary_anatomic_site
- Peritoneal Cavity [NCIt concept]
- Peritoneum [NCIt concept]
disease_may_have_cytogenetic_abnormality
- Gain of Chromosome 17q [NCIt concept]
- Gain of Chromosome 1q [NCIt concept]
- Gain of Chromosome 5p [NCIt concept]
- Gain of Chromosome 7p [NCIt concept]
- Gain of Chromosome 8q [NCIt concept]
- Loss of Chromosome 13q [NCIt concept]
- Loss of Chromosome 14q [NCIt concept]
- Loss of Chromosome 1p [NCIt concept]
- Loss of Chromosome 22q [NCIt concept]
- Loss of Chromosome 3p [NCIt concept]
- Loss of Chromosome 4q [NCIt concept]
- Loss of Chromosome 6q [NCIt concept]
- Loss of Chromosome 9p [NCIt concept]
disease_may_have_molecular_abnormality
- BAP1 Gene Mutation [NCIt concept]
- CDKN2A Gene Inactivation [NCIt concept]
- NF2 Gene Inactivation [NCIt concept]

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