Childhood Hepatoblastoma by Toronto Guidelines v2 Stage, Tier 2

Preferred Label : Childhood Hepatoblastoma by Toronto Guidelines v2 Stage, Tier 2;

NCIt synonyms : Pediatric Hepatoblastoma by Toronto Guidelines v2 Stage, Tier 2;

NCIt definition : A term that refers to the staging of childhood hepatoblastoma according to the tier 2 Toronto childhood cancer staging guidelines v2. It includes localized tumors, metastatic tumors, and the PRETEXT system. (Childhood cancer staging for population registries according to the Toronto Childhood Cancer Stage Guidelines - Version 2. Cancer Council Queensland and Cancer Australia: Brisbane, Australia; 2021.);

Neoplastic status : Malignant;

NCI Metathesaurus CUI : CL1914009;

Details

Origin ID

C198190;

UMLS CUI

C5786885;

Disease may have findings
- Abdominal Mass [NCIt concept]
- Anorexia [NCIt concept]
- Diaphragmatic Hernia [NCIt concept]
- Jaundice [NCIt concept]
- Meckel Diverticulum [NCIt concept]
- Thrombocytosis [NCIt concept]
- Weight Loss [NCIt concept]
Excludes anatomical site(s)
- Extrahepatic Bile Duct [NCIt concept]
Has associated anatomic sites
- Digestive System [NCIt concept]
- Hepatobiliary System [NCIt concept]
- Liver [NCIt concept]
Semantic type(s)
- Classification [UMLS semantic type]
disease_excludes_finding
- Benign Cellular Infiltrate [NCIt concept]
disease_excludes_normal_tissue_origin
- Germinal Layer [NCIt concept]
disease_has_abnormal_cell
- Malignant Cell [NCIt concept]
- Neoplastic Cell [NCIt concept]
disease_has_finding
- Childhood Lesion [NCIt concept]
- Malignant Cellular Infiltrate [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
- Liver [NCIt concept]
disease_is_stage
- Toronto Classification v2 Stage [NCIt concept]
- Toronto Classification v2 Stage, Tier 2 [NCIt concept]
disease_mapped_to_gene
- CTNNB1 Gene [NCIt concept]
disease_may_have_associated_disease
- Anemia [NCIt concept]
- Inguinal Hernia [NCIt concept]
disease_may_have_cytogenetic_abnormality
- Loss of Chromosome 11p [NCIt concept]
- Trisomy 2 [NCIt concept]
- Trisomy 20 [NCIt concept]
disease_may_have_molecular_abnormality
- CTNNB1 Gene Mutation [NCIt concept]
- NFE2L2 Gene Mutation [NCIt concept]
- TERT Promoter Mutation [NCIt concept]

Keyword's position in hierarchy(ies) :

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