Fetal Rhabdomyoma

Preferred Label : Fetal Rhabdomyoma;

NCIt definition : A rare benign mesenchymal neoplasm arising from skeletal muscle. It is characterized by the presence of immature spindle and polygonal cells within a scant myxoid stroma. It usually develops in the head and neck region of young children.;

Neoplastic status : Benign;

ICD-O code : 8903/0;

Details

Origin ID

C4260;

UMLS CUI

C0334482;

Automatic exact mappings (from CISMeF team)
- Fetal rhabdomyoma [ICD-9 code]
- Fetal rhabdomyoma [ICD-11 Extension code]
- Fetal rhabdomyoma [ICD-11 More detail]
- Fetal rhabdomyoma (disorder) [SNOMED CT concept]
Currated CISMeF NLP mapping
- Fetal rhabdomyoma [ICD-O code]
- Fetal rhabdomyoma (morphologic abnormality) [SNOMED CT concept]
- fetal rhabdomyoma [SNOMED Notion]
Disease excludes abnormal cell
- Malignant Cell [NCIt concept]
- Neoplastic Large Striated Muscle Cell with Clear Cytoplasm [NCIt concept]
- Spider Cell [NCIt concept]
Disease excludes normal cell origin
- Neuron, Neuroepithelial Cell, and Supporting Cell of the Nervous System [NCIt concept]
Excludes anatomical site(s)
- Bone [NCIt concept]
- Heart [NCIt concept]
Has associated anatomic sites
- Connective and Soft Tissue [NCIt concept]
- Musculoskeletal System [NCIt concept]
Semantic type(s)
- Neoplastic Process [UMLS semantic type]
UMLS correspondences (same concept)
- Fetal rhabdomyoma [ICD-O code]
- Fetal rhabdomyoma (disorder) [SNOMED CT concept]
- Fetal rhabdomyoma (morphologic abnormality) [SNOMED CT concept]
- fetal rhabdomyoma [SNOMED Notion]
concept_is_in_subset
- GDC Terminology [NCIt concept]
- GDC Value Terminology [NCIt concept]
- Mapped ICDO3.1 Morphology PT Terminology [NCIt concept]
- Mapped ICDO3.1 Morphology Terminology [NCIt concept]
- Mapped ICDO3.1 Terminology [NCIt concept]
- Mapped ICDO3.2 Morphology PT Terminology [NCIt concept]
- Mapped ICDO3.2 Morphology Terminology [NCIt concept]
- Mapped ICDO3.2 Terminology [NCIt concept]
disease_excludes_finding
- Malignant Cellular Infiltrate [NCIt concept]
disease_has_abnormal_cell
- Neoplastic Cell [NCIt concept]
- Neoplastic Connective and Soft Tissue Cell [NCIt concept]
- Neoplastic Muscle Cell [NCIt concept]
- Neoplastic Skeletal Muscle Cell [NCIt concept]
disease_has_finding
- Benign Cellular Infiltrate [NCIt concept]
- Indolent Clinical Course [NCIt concept]
- Well-Circumscribed Lesion [NCIt concept]
disease_has_molecular_abnormality
- PTCH1 Gene Mutation [NCIt concept]
disease_has_normal_cell_origin
- Connective and Soft Tissue Cell [NCIt concept]
- Muscle Cell [NCIt concept]
- Skeletal Muscle Cell [NCIt concept]
- Striated 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]
- Striated Muscle Tissue [NCIt concept]
disease_has_primary_anatomic_site
- Musculoskeletal System [NCIt concept]
disease_mapped_to_gene
- PTCH1 Gene [NCIt concept]
may_be_associated_disease_of_disease
- Nevoid Basal Cell Carcinoma Syndrome [NCIt concept]
pathogenesis_of_disease_involves_gene
- PTCH1 Gene [NCIt concept]
- PTCH1 wt Allele [NCIt concept]

Keyword's position in hierarchy(ies) :

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