About: Rhabdomyosarcoma

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Attributes	Values
rdf:type	Class
rdfs:label	Rhabdomyosarcoma
equivalentClass	nodeID://b638100
Has_NICHD_Parent	Neoplasm
Concept_In_Subset	NCI CTEP Simplified Disease Classification Terminology NCI CTEP SDC Rhabdomyosarcoma Sub-Category Terminology Clinical Data Interchange Standards Consortium Terminology CDISC SDTM Terminology CDISC SEND Terminology CDISC SEND Tumor Findings Results Terminology NICHD Terminology Neonatal Research Network Terminology
Semantic_Type	Neoplastic Process
Preferred_Name	Rhabdomyosarcoma
UMLS_CUI	C0035412
Contributing_Source	CDISC CTEP NICHD
ALT_DEFINITION	A malignant mesenchymal neoplasm arising from skeletal muscle.CDISC Cancer that forms in the soft tissues in a type of muscle called striated muscle. Rhabdomyosarcoma can occur anywhere in the body.NCI-GLOSS A malignant tumor showing skeletal muscle tumor differentiation and which does not show classic histologic features of described rhabdomyosarcoma subtypes (e.g. embryonal, alveolar). This term may be used for small biopsy specimens for which adequate tissue is not present for definitive classification.NCI
ICD-O-3_Code	8900/3
Neoplastic_Status	Malignant
Legacy_Concept_Name	Rhabdomyosarcoma
FULL_SYN	Rhabdomyosarcoma, NOSPTCTEP10039024 RhabdomyosarcomaPTNCI RHABDOMYOSARCOMA, MALIGNANTPTCDISC RhabdomyosarcomaPTNICHD rhabdomyosarcomaPTNCI-GLOSSCDR0000045872
DEFINITION	A rare aggressive malignant mesenchymal neoplasm arising from skeletal muscle. It usually occurs in children and young adults. Only a small percentage of tumors arise in the skeletal muscle of the extremities. The majority arise in other anatomical sites.NCI
code	C3359
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