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| Term | rhabdomyosarcoma | ID (Ontology) | DOID:3247 (Human Disease) |
| Definition | A skeletal muscle cancer that arise from skeletal muscle progenitors. | ||
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Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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cell type cancer |__sarcoma_________________ muscle cancer | |__skeletal muscle cancer__| rhabdomyosarcoma 24 rec. |__alveolar rhabdomyosarcoma 24 rec. |__anus rhabdomyosarcoma |__bile duct rhabdomyosarcoma | |__embryonal extrahepatic bile duct rhabdomyosarcoma |__central nervous system rhabdomyosarcoma |__embryonal rhabdomyosarcoma | |__botryoid rhabdomyosarcoma(+) | |__parameningeal embryonal rhabdomyosarcoma |__gallbladder rhabdomyosarcoma |__mediastinum rhabdomyosarcoma |__mixed type rhabdomyosarcoma |__oral rhabdomyosarcoma |__ovary rhabdomyosarcoma |__pleomorphic rhabdomyosarcoma | |__adult pleomorphic rhabdomyosarcoma | |__childhood pleomorphic rhabdomyosarcoma |__spindle cell rhabdomyosarcoma |
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| Is a |
sarcoma skeletal muscle cancer |
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External Crossreferences & Linkouts
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ICDO:8900/3 MESH:D012208 NCI:C3359 SNOMEDCT_US_2023_03_01:302847003 UMLS_CUI:C0035412 |
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