Pleural Biphasic Mesothelioma

Preferred Label : Pleural Biphasic Mesothelioma;

NCIt definition : Malignant mesothelioma that arises from the pleura. It is characterized by the presence of epithelioid and sarcomatoid components, with each component representing at least 10% of the tumor.;

Neoplastic status : Malignant;

Détails

Origin ID

C45665;

UMLS CUI

C1709570;

Currated CISMeF NLP mapping
- biphasic pleural mesothelioma [Disease (Nov.)]
Disease may have findings
- Anorexia [NCIt concept]
- Chest Pain [NCIt concept]
- Chills [NCIt concept]
- Dyspnea [NCIt concept]
- Fatigue [NCIt concept]
- Malaise [NCIt concept]
- Pleural Effusion [NCIt concept]
- Sweating [NCIt concept]
- Weight Loss [NCIt concept]
Excludes anatomical site(s)
- Neck [NCIt concept]
Has associated anatomic sites
- Pleural Cavity [NCIt concept]
- Respiratory System [NCIt concept]
- Thoracic Cavity [NCIt concept]
Semantic type(s)
- Neoplastic Process [UMLS semantic type]
UMLS correspondences (same concept)
- biphasic pleural mesothelioma [Disease (Nov.)]
concept_is_in_subset
- CTRP Disease Terminology [NCIt concept]
- CTRP Terminology [NCIt concept]
- Cellosaurus Disease Terminology [NCIt concept]
disease_excludes_finding
- Benign Cellular Infiltrate [NCIt concept]
disease_has_abnormal_cell
- Malignant Cell [NCIt concept]
- Malignant Mesothelial Cell [NCIt concept]
- Neoplastic Cell [NCIt concept]
- Neoplastic Mesothelial Cell [NCIt concept]
disease_has_finding
- Biphasic Pattern [NCIt concept]
- Diffuse Pattern [NCIt concept]
- Malignant Cellular Infiltrate [NCIt concept]
disease_has_normal_cell_origin
- Mesothelial Cell [NCIt concept]
disease_has_normal_tissue_origin
- Mesothelium [NCIt concept]
- Pleura [NCIt concept]
disease_has_primary_anatomic_site
- Pleural Cavity [NCIt concept]
disease_may_have_cytogenetic_abnormality
- Gain of Chromosome 15q [NCIt concept]
- 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 1 [NCIt concept]
- Loss of Chromosome 13q [NCIt concept]
- Loss of Chromosome 14q [NCIt concept]
- Loss of Chromosome 17p [NCIt concept]
- Loss of Chromosome 1p [NCIt concept]
- Loss of Chromosome 22q [NCIt concept]
- Loss of Chromosome 3 [NCIt concept]
- Loss of Chromosome 3p [NCIt concept]
- Loss of Chromosome 4q [NCIt concept]
- Loss of Chromosome 6q [NCIt concept]
- Loss of Chromosome 9 [NCIt concept]
- Loss of Chromosome 9p [NCIt concept]
- Monosomy 22 [NCIt concept]
disease_may_have_molecular_abnormality
- BAP1 Gene Mutation [NCIt concept]
- CDKN2A Gene Inactivation [NCIt concept]
- Inactivating GPC3 Gene Mutation [NCIt concept]
- NF2 Gene Inactivation [NCIt concept]
- NF2 Gene Mutation [NCIt concept]

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

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