Childhood Embryonal Rhabdomyosarcoma

Preferred Label : Childhood Embryonal Rhabdomyosarcoma;

NCIt synonyms : Pediatric Embryonal Rhabdomyosarcoma; Embryonal Childhood Rhabdomyosarcoma;

NCIt related terms : Embryonal Rhabdomyosarcoma;

NCIt definition : A poorly circumscribed morphologic variant of rhabdomyosarcoma occurring in children. The neoplasm is characterized by the presence of primitive skeletal muscle in any stage of myogenesis.;

Alternative definition : NICHD: A poorly circumscribed morphologic variant of rhabdomyosarcoma that generally arises in the head and neck region or in the genitourinary tract.;

Neoplastic status : Malignant;

Details

Origin ID

C7957;

UMLS CUI

C0279612;

Automatic exact mappings (from CISMeF team)
- Embryonal rhabdomyosarcoma [PASCAL descriptor]
- Embryonal rhabdomyosarcoma [MedDRA Preferred Term]
- Embryonal rhabdomyosarcoma [HPO term]
- Embryonal rhabdomyosarcoma [ICD-O code]
- Embryonal rhabdomyosarcoma [ORDO Disease]
- Embryonal rhabdomyosarcoma [ICD-9 code]
- Embryonal rhabdomyosarcoma (disorder) [SNOMED CT concept]
- Embryonal rhabdomyosarcoma (morphologic abnormality) [SNOMED CT concept]
- embryonal rhabdomyosarcoma [DO Concept]
- embryonal rhabdomyosarcoma [SNOMED Notion]
- rhabdomyosarcoma, embryonal [MeSH Descriptor]
- rhabdomyosarcoma, embryonal [MeSH concept]
Disease excludes normal cell origin
- Epithelial Cell [NCIt concept]
- Neuron, Neuroepithelial Cell, and Supporting Cell of the Nervous System [NCIt concept]
Excludes anatomical site(s)
- Bone [NCIt concept]
Has associated anatomic sites
- Connective and Soft Tissue [NCIt concept]
- Musculoskeletal System [NCIt concept]
Has cytogenetic abnormalities
- Loss of Chromosome 11p [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]
- Intermediate Filaments Present [NCIt concept]
- Intracytoplasmic Eosinophilic Inclusion [NCIt concept]
- Well-Circumscribed Lesion [NCIt concept]
disease_excludes_normal_tissue_origin
- Epithelial Tissue [NCIt concept]
disease_has_abnormal_cell
- Malignant Cell [NCIt concept]
- Malignant Rhabdomyoblast [NCIt concept]
- Malignant Skeletal Muscle Cell [NCIt concept]
- Neoplastic Cell [NCIt concept]
- Neoplastic Connective and Soft Tissue Cell [NCIt concept]
- Neoplastic Muscle Cell [NCIt concept]
- Neoplastic Skeletal Muscle Cell [NCIt concept]
- Primitive Malignant Skeletal Muscle Cell [NCIt concept]
disease_has_finding
- Childhood Lesion [NCIt concept]
- High Grade Lesion [NCIt concept]
- Malignant Cellular Infiltrate [NCIt concept]
- Rapidly Enlarging Mass [NCIt concept]
disease_has_normal_cell_origin
- Connective and Soft Tissue Cell [NCIt concept]
- Muscle Cell [NCIt concept]
- Skeletal Muscle Cell [NCIt concept]
disease_has_normal_tissue_origin
- Connective and Soft Tissue [NCIt concept]
- Muscle Tissue [NCIt concept]
- Skeletal Muscle Tissue [NCIt concept]
- Soft Tissue [NCIt concept]
disease_may_have_cytogenetic_abnormality
- Rearrangement of 12q13 [NCIt concept]
- Rearrangement of 1p11-q11 [NCIt concept]
- del(11p15) [NCIt concept]
disease_may_have_molecular_abnormality
- FGFR4 Gene Mutation [NCIt concept]

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