Hepatocellular Malignant Neoplasm, Not Otherwise Specified

Preferred Label : Hepatocellular Malignant Neoplasm, Not Otherwise Specified;

NCIt synonyms : HCN-NOS; Hepatocellular Malignant Neoplasm, NOS; HEMNOS;

NCIt definition : A rare childhood malignant liver neoplasm with overlapping features of hepatoblastoma and hepatocellular carcinoma.;

Neoplastic status : Malignant;

Concept status : Provisional_Concept;

NCI Metathesaurus CUI : CL970394;

Details

Origin ID

C161838;

UMLS CUI

C5206136;

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]
False automatic mappings
- hemin [MeSH Descriptor]
Has associated anatomic sites
- Digestive System [NCIt concept]
- Hepatobiliary System [NCIt concept]
- Liver [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_excludes_normal_tissue_origin
- Germinal Layer [NCIt concept]
disease_has_abnormal_cell
- Adenocarcinoma Cell [NCIt concept]
- Malignant Cell [NCIt concept]
- Neoplastic Cell [NCIt concept]
disease_has_finding
- Childhood Lesion [NCIt concept]
- Malignant Cellular Infiltrate [NCIt concept]
- Morphologic Overlap [NCIt concept]
- Not Otherwise Specified Lesion [NCIt concept]
disease_has_normal_cell_origin
- Embryonic Cell [NCIt concept]
- Hepatocyte [NCIt concept]
disease_has_normal_tissue_origin
- Embryonic Tissue [NCIt concept]
disease_has_primary_anatomic_site
- Liver [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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