Hepatoblastoma with Pure Fetal Epithelial Differentiation

Preferred Label : Hepatoblastoma with Pure Fetal Epithelial Differentiation;

NCIt definition : A hepatoblastoma composed of small cells resembling the fetal hepatocytes, forming thin trabeculae.;

Alternative definition : NICHD: A hepatoblastoma comprising small cells resembling the fetal hepatocytes, forming thin trabeculae.;

Neoplastic status : Malignant;

ICD-O code : 8970/3;

Détails

Origin ID

C7093;

UMLS CUI

C1333982;

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)
- Neoplastic Process [UMLS semantic type]
concept_is_in_subset
- NICHD Terminology [NCIt concept]
- Pediatric Hematology-Oncology Terminology [NCIt concept]
disease_excludes_finding
- Benign Cellular Infiltrate [NCIt concept]
- Mesenchymal Component Present [NCIt concept]
disease_excludes_normal_tissue_origin
- Germinal Layer [NCIt concept]
disease_has_abnormal_cell
- Malignant Cell [NCIt concept]
- Neoplastic Cell [NCIt concept]
- Small Cuboidal Cell Resembling Fetal Hepatocyte [NCIt concept]
disease_has_finding
- Childhood Lesion [NCIt concept]
- Epithelial Component Present [NCIt concept]
- Fetal -Epithelial Differentiation [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]
- Hepatobiliary Tissue [NCIt concept]
disease_has_primary_anatomic_site
- Hepatobiliary System [NCIt concept]
- 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]

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

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