Childhood Atypical Teratoid/Rhabdoid Tumor

Preferred Label : Childhood Atypical Teratoid/Rhabdoid Tumor;

NCIt synonyms : Childhood Atypical Teratoid Rhabdoid Tumor;

NCIt related terms : Atypical Teratoid/Rhabdoid Tumor;

NCIt definition : An atypical teratoid/rhabdoid tumor occurring in children.;

Alternative definition : NICHD: A rare, clinically aggressive tumor of the CNS that most often affects children aged 3 years and younger, but that can occur in older children and adults.;

Neoplastic status : Malignant;

NCI Metathesaurus CUI : CL372028;

Details

Origin ID

C68634;

UMLS CUI

C2347613;

Automatic exact mappings (from CISMeF team)
- Atypical teratoid rhabdoid tumor [ORDO Disease]
- Atypical teratoid/rhabdoid tumor [ORDO Disease]
- Atypical teratoid/rhabdoid tumor [ICD-O code]
- Atypical teratoid/rhabdoid tumor (morphologic abnormality) [SNOMED CT concept]
- atypical teratoid rhabdoid tumor [DO Concept]
- atypical teratoid rhabdoid tumor [Radlex concept]
Disease may have findings
- Aggressive Clinical Course [NCIt concept]
- High Mitotic Activity [NCIt concept]
- Loss of BRG1 Protein Expression [NCIt concept]
- Loss of INI 1 Protein Expression [NCIt concept]
- Necrotic Change [NCIt concept]
Has associated anatomic sites
- Central Nervous System [NCIt concept]
- Nervous System [NCIt concept]
Semantic type(s)
- Neoplastic Process [UMLS semantic type]
concept_is_in_subset
- CTRP Disease Terminology [NCIt concept]
- CTRP Terminology [NCIt concept]
- NICHD Terminology [NCIt concept]
- Pediatric Hematology-Oncology Terminology [NCIt concept]
disease_excludes_finding
- Benign Cellular Infiltrate [NCIt concept]
- Indolent Clinical Course [NCIt concept]
disease_excludes_normal_tissue_origin
- Germinal Layer [NCIt concept]
disease_has_abnormal_cell
- Malignant Cell [NCIt concept]
- Malignant Cell with Large Nucleus and Abundant Eosinophilic Cytoplasm [NCIt concept]
- Malignant Neuroectodermal Cell [NCIt concept]
- Neoplastic Cell [NCIt concept]
disease_has_finding
- Childhood Lesion [NCIt concept]
- Intermediate Filaments Present [NCIt concept]
- Intracytoplasmic Eosinophilic Inclusion [NCIt concept]
- Malignant Cellular Infiltrate [NCIt concept]
disease_has_grade
- Grade 4 [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
- Central Nervous System [NCIt concept]
disease_mapped_to_gene
- SMARCA4 Gene [NCIt concept]
- SMARCB1 Gene [NCIt concept]
disease_may_have_abnormal_cell
- Non-Neoplastic Osteoclast-Like Giant Cell [NCIt concept]
disease_may_have_cytogenetic_abnormality
- Loss of Chromosome 22 [NCIt concept]
disease_may_have_molecular_abnormality
- SMARCA4 Gene Mutation [NCIt concept]
- SMARCB1 Gene Mutation [NCIt concept]

Keyword's position in hierarchy(ies) :

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